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Pharmaceuticals
  • Review
  • Open Access

23 October 2023

The Use of Shells of Marine Molluscs in Spanish Ethnomedicine: A Historical Approach and Present and Future Perspectives

and
1
Grupo de Investigación de Recursos Etnobiológicos del Duero-Douro (GRIRED), Facultad de Biología, Universidad de Salamanca, E-37071 Salamanca, Spain
2
Departamento de Anatomía Patológica, Biología Celular, Histología, Historia de la Ciencia, Medicina Legal y Forense y Toxicología, Área de Historia de la Ciencia, Facultad de Medicina, Universidad de Cádiz, E-11003 Cádiz, Spain
*
Author to whom correspondence should be addressed.
This article belongs to the Special Issue Plant and Marine-Derived Natural Product Research in Drug Discovery: Strengths and Perspective

Abstract

Since ancient times, the shells of marine molluscs have been used as a therapeutic and/or prophylactic resource. In Spain, they were part of practical guides for doctors or pharmacists until the 19th century. In general, seashells were prepared by dissolving in vinegar and were part of plasters or powders used as toothpaste, or to treat dyspepsia, heartburn and leprosy. Thus, the nacre or mother-of-pearl of various molluscs was regularly used in the Royal Colleges of Surgery and in hospitals during the times of the Cortes of Cadiz, as a medicine in galenic preparations based on powders. In contemporary Spanish ethnomedicine, seashells, with a high symbolic value, have been used as an amulet to prevent cracks in the breasts and promote their development during lactation, to avoid teething pain in young children, to eliminate stains on the face or to cure erysipelas. But, as in other countries, products derived from seashells have also been empirically applied. The two resources used traditionally have been the cuttlebone, the internal shell of cuttlefish and the nacre obtained from the external shells of some species. Cuttlebone, dried and pulverised, has been applied externally to cure corneal leukoma and in dental hygiene. In the case of nacre, a distinction must be made between chemical and physical remedies. Certain seashells, macerated in lemon juice, were used in coastal areas to remove spots on the face during postpartum. However, the most common practice in Spain mainland was to dissolve mother-of-pearl buttons in lemon juice (or vinegar). The substance thus obtained has been used to treat different dermatological conditions of the face (chloasma, acne), as well as to eliminate freckles. For the extraction of foreign bodies in the eyes, a very widespread traditional remedy has been to introduce small mother-of-pearl buttons under the lid. These popular remedies and practices are compared with those collected in classic works of medicine throughout history, and data on the pharmacological activity and pharmaceutical applications of the products used are provided. The use of cuttlebone powders is supported by different works on anti-inflammatory, immune-modulatory and/or wound healing properties. Nacre powder has been used in traditional medicines to treat palpitations, convulsions or epilepsy. As sedation and a tranquilisation agent, nacre is an interesting source for further drug development. Likewise, nacre is a biomaterial for orthopaedic and other tissue bioengineering applications. This article is a historical, cultural and anthropological view that can open new epistemological paths in marine-derived product research.

1. Introduction

In contemporary Spanish ethnomedicine, only a single use-report concerning the medical use of an entire marine mollusc has been documented. So, in Bedarona (Biscay), when they had warts on their hands, they collected limpets (genus Patella, Gastropoda, Patellidae) on the rocks along the coast. With each of these snails they rubbed a particular wart several times, and then killed them by poking them with a stick, in the belief that when the limpets rotted the warts would disappear [1]. However, in Spain, the most important therapeutic resource for this group of invertebrate animals has been their shells.

Symbolisms Associated with Shells

There is evidence and data on the use of seashells in different societies since time immemorial. Thus, we find studies on archaeozoology that show that the coastal malacofauna (molluscs) was used in the eastern part of the Iberian Peninsula from the Neolithic Age to the end of the Bronze Age for the manufacture of ornamental elements, and with a value linked to the world of symbolism and magic [2]. In some cases, they were personal attributes of an ornamental, aesthetic, ideological or symbolic nature of the amulet type [3,4]. It is evident that the world of beliefs, symbols and amulets form part of the first medical manifestations and that they have endured through the history of therapeutics [5,6]. In this way, since ancient times, the shells of marine molluscs have been used in the Mediterranean region as an apotropaic amulet to preserve both humans and domestic animals from harm and disease [5,7].
For this reason, it is very interesting to combine the methodologies of anthropology and history to study the traditions of popular culture. In the case of the symbolism associated with seashells, we can obtain a whole series of cultural interpretations of the historical experience. For example, because of its clear resemblance, shape and colouring, reminiscent of a woman’s vulva, the shell combines sexual symbolism with the idea of procreation and fertility. All this makes it the attribute of the goddess of love: Aphrodite-Venus materialises by emerging from the foam of the ocean and, placed in a shell, is carried to the mainland [8,9,10,11].
Paleo-Christian art made the empty shell an image of the departure of the soul to immortality [10], a symbol of birth into the future life, of the resurrection [8]. Christian symbolism saw the shell as the image of the sepulchre that embraces man after death before he can be resurrected [9]. As a symbol of fertility, the shell also became a symbol and attribute of the Virgin Mary [9,11].

2. Taxonomy and Uses in Folk Medicine

2.1. Magical Uses

Popularly known as the caracol de viento (“wind snail”), hung around the neck, it was used in various Spanish regions as a superstitious remedy to prevent teething pain in small children, to cure erysipelas and to remove spots from the face [12,13].
In 1883, in his work Supersticiones populares recogidas en Andalucía y comparadas con las portuguesas (“Popular superstitions collected in Andalusia and compared with those of Portugal”), the folklorist Alejandro Guichot y Sierra noted that he had heard this usage said in public to a shell seller in Seville, a seller who had a tarpaulin stretched on the ground on which piles of various seashells were displayed, and who was listened to by a large group of curious onlookers [14].
On the other hand, it is worth mentioning that there are many traditional methods used in Spain to prevent cracks in the breasts during breastfeeding, and different amulets have also been used which, according to popular belief, prevent them from appearing.
The similia similibus curantur (“likes are cured by likes”) principle can be applied to almost all of the amulets used for this purpose, since they are objects which, because of their resemblance to healthy and voluminous breasts, were used to prevent them from deteriorating and to facilitate their firming and resistance to the effects of breast-feeding [15,16]. In the present work we must point out the use of the shells of small marine molluscs, especially those of some representative species of the family Cypraeidae, commonly named cowries, and the shells of cockles (the common cockle, Cerastoderma edule (Linnaeus, 1758)), but also the use of those commonly known as buguinas, i.e., large and edible marine gastropods as the common whelk (Buccinum undatum Linnaeus, 1758; Buccinidae) or the knobbed triton (Charonia lampas (Linnaeus, 1758); Charoniidae) [17].

2.2. Empirical Remedies

In contemporary Spanish ethnomedicine, products derived from seashells have been used—applied in an empirical way—specifically the cuttlebone, the internal shell of cuttlefish (Sepia officinalis Linnaeus, 1758; Cephalopoda, Sepiidae) and the nacre (or mother-of-pearl) from the shells of certain species (e.g., Pinna nobilis Linnaeus, 1758; Haliotis tuberculata Linnaeus, 1758) (Figure 1).
Figure 1. Examples of zootherapeutic resources of marine origin used in contemporary Spanish ethnomedicine: (a) internal shell of the cuttlefish; (b) inner iridescent “mother-of-pearl” layer of the ear-shaped shell of the green ormer (Haliotis tuberculata); (c) detail of the interior surface of the shell of the noble pen shell (Pinna nobilis) (photos by J.A. González); (d) worn-out shell of a large oyster in which the nacreous layer is visible (photo by J.R. Vallejo).

2.2.1. The Cuttlebone in Spanish Ethnomedicine

Known in Spain by the names sepión, jibión or hueso de la jibia, the cuttlebone has been a zootherapeutic resource in Spanish ethnoveterinary medicine. Dried and pulverised, the cuttlebone has been applied externally (topical use) to cure corneal ulcers, infectious bovine keratoconjunctivitis (“pinkeye”) and udder injuries, and by its internal use to treat aphthous fever in cattle [18].
In the field of ethnomedicine, we find a reference to its use in the treatment of corneal leucoma. So, in Tenerife (Canary Islands), lesions appearing on the cornea as a result of a blow or injury were treated by applying the powder obtained from grinding this internal shell to the affected eye [19,20].
In Asturias, this powder was used to clean teeth, for dental hygiene [21].

2.2.2. Nacre in Spanish Ethnomedicine

The seashells richest in nacre were used in folk dermatology; they constituted a popular remedy for removing spots on the face that can be classified as “chemical”. Certain shells were macerated in lemon juice.
In Palamós (Gerona), women would fight against postpartum spots (melasma or chloasma) by applying a white paste obtained by macerating curculles de nacre (mother-of-pearl shells) in lemon juice for 9 or 10 days [22].
Nevertheless, due to the difficulty of obtaining mother-of-pearl shells far from the coast, or simply because it was a readily available resource, mother-of-pearl buttons were also dissolved in lemon juice or vinegar to obtain the remedy. So, in Extremadura, different types of pimples and acne were treated by applying the paste obtained from dissolving several mother-of-pearl buttons in lemon juice or vinegar to the affected areas [23,24,25].
To cure eczema, in the Canary Islands, they put a mother-of-pearl button in lemon juice and left the container in the open air all night. By dawn, the button had dissolved, and the substance obtained could then be used [26,27].
To make freckles, considered to be ugly or rather unattractive, disappear from the face, in the provinces of Cádiz [28], Badajoz [29] and Málaga [30], but also in far off Navarre [1], the face was washed with the mixture obtained by macerating one or more mother-of-pearl buttons in lemon juice. The glass was left in the open air overnight, and the following morning, when the buttons had melted, the liquid obtained was applied to the area where the freckles were. The treatment had to be repeated for at least a week.
The other field of ethnomedicine in which seashells very rich nacre were used is popular ophthalmology. In this case, we have to talk of a “physical-mechanical” type of remedy for the removal of foreign bodies from the eyes.
The nutlets (mericarps) of salvia, principally of the species Salvia verbenaca L., have been the most widespread remedy in Spain for the removal of foreign bodies from the eyes. Small in size (1.6–2.4 mm), producing mucilaginous and very soft substances, and popularly known as “eye-cleaners”, they have also been used to clean eyes in other parts of the Mediterranean region [31,32,33]. When a foreign body (an eyelash, dust, straw, etc.) enters the eye, a nutlet was placed under the lid to force it out. This practice was especially important in past decades when hand threshing and winnowing were still carried out in our country [34,35].
Continuing the importance of their use, we should also mention in this review the mechanical use of small mother-of-pearl buttons to remove foreign bodies from the eyes. So, if something got into the eye while working in the field, a small mother-of-pearl button was placed under the eyelid. This practice has been documented in Extremadura [24,36,37,38,39] and in the provinces of Alicante [40] and Soria [41].
In contrast, in Humanes (Guadalajara), they would insert a mother-of-pearl button into the eye when they had a stye, “to break its head”, i.e., with the aim of reducing the inflammation and releasing the pus that these painful eye conditions usually contain [42].

4. Medicinal Properties, Modern Uses and Perspectives

Many mollusc-derived products have an extensive array of therapeutic properties, including antimicrobial, antioxidant, anticancer, anti-inflammatory, antihypertensive, wound healing and other medicinal properties [94,95,96,97]. As a result of a significant evolutionary divergence, the phylum Mollusca includes numerous and very diverse groups de marine invertebrates. Associated with this is their very significant chemical diversity. Marine molluscs, for example, use secondary metabolites to communicate and defend themselves against predators and microbial pathogens [98,99], and they have become the focus of many chemical studies aimed at isolating and identifying novel natural products. This highlights the need for further research to identify the chemical compounds of certain molluscan species to provide leads for novel drugs and biomaterials in the future.

4.1. Cuttlebone

Cuttlefish bone is composed primarily of aragonite (crystal forms of calcium carbonate) and β-chitin, and it has a very elaborate microstructure. Many sea invertebrates have very characteristic internal shells, but the cuttlebone is unique due to its chambered complex structure [100,101,102,103]. Commonly used as a calcium-rich dietary supplement for caged animals (birds, turtles) and as a grinding stone for the beaks of cage birds [104], cuttlebone combining high porosity with high compressive strength is a very interesting material from the biomimetic materials’ technology point of view [100,101,104].

4.1.1. Pharmacological Activity and Pharmaceutical Applications

Cuttlebone is especially important in the field of promoting bone healing. Various studies reveal the potential of different biomaterials derived from cuttlebone to deliver 3D scaffolds with potential for bone formation and regeneration applications [105,106]. Cuttlebone-derived scaffolds are popular due to their biocompatibility and high regenerative potential.
Bone grafting is widely used to bridge major bone defects or to promote bone union. Concerning biocompatibility, fibrous capsules of hydroxyapatite from cuttlebone are a valuable bone graft material. Cuttlebone-derived hydroxyapatite, prepared from cuttlebone via hydrothermal transformation [107,108], is an appropriate biomaterial to stimulate bone formation and enhance bone regeneration [108]. For its effective osteoconduction, cuttlebone-derived hydroxyapatite is a safe material for use inside the body [109].
Alginate capsules with cuttlebone-derived fillers have been developed for bone repair applications. Prepared capsules are designed to be suitable for the treatment of small-sized bone loss provocative diseases, such as endodontic and periodontal diseases [110]. Proliferative and osteoconductive effects on the osteoblast-like MG-63 cells demonstrate the cellulose/cuttlebone scaffolds soaked in simulated body fluid as a favourable material for bone tissue engineering [111].
It has been discovered that cuttlefish bones are an excellent resource for producing desirable amounts of chitin and chitosan. Chitosan, a chitin-derived linear cationic polysaccharide, is a natural, hydrophilic, non-allergenic, biocompatible, non-toxic and biodegradable product obtained from chitin of cuttlebone [112,113]. Chemical modification of chitosan has been frequently carried out to prepare derivatives with applications in many fields including pharmaceutics [112,114,115,116]. For example, a low-molecular weight sulfated chitosan holds immense potential in carbohydrate-based pharmaceuticals [117], and it is a potential inhibitor of white spot syndrome virus proteins [118].
Likewise, antimicrobial activities of powdered cuttlebone have been demonstrated, and it can be used as an accessible natural source to provide novel, low-cost and safe antimicrobial agents [119]. For example, powdered cuttlebone has been found to be effective against the bacterium Klebsiella oxytoca, and antifungal activity against Aspergillus flavus has been also recorded [120].
Anti-inflammatory, immune-modulatory and wound healing activities of cuttlebone have been shown [97]. Cuttlebone is a valuable material for the treatment of skin wound such as ulcer lesions and burn injuries [121,122]. Cuttlebone extracts stimulated wound skins to induce acute inflammation and to promoted cell proliferation and matrix metalloproteases expression in fibroblast [122].
Prepared formulations from cuttlebone showed appropriate physicochemical properties and high antacid capacity. Then, as proposed by Mostoufi et al. [123], we can use formulations of cuttlefish bone as a good natural antacid drug that has fewer side effects, has high efficiency, is inexpensive, and is comparable with the marketed tablets and other antacid compounds.

4.1.2. Environmental Utilization

The cuttlebone has a high environmental value. It can be useful in bioecological research, providing reliable information on environmental conditions. For example, the isotope composition of cuttlebone aragonite appears to be in isotopic equilibrium with the ambient seawater [124], and stable carbon and oxygen isotopes from it are natural tags for determining the degree of spatial connectivity between nearshore and offshore environments [125].
Cuttlebone is an effective bio-adsorbent, constituting an efficient, low-cost and eco-friendly technology for reducing copper pollution during wastewater treatment [126]. A superhydrophobic and oleophilic porous material obtained using biomass cuttlebone as a scaffold has an excellent oil–water separation efficiency [127]. This finding is important for the elimination of spills of crude oil and other marine organic pollutants, very common around the world and resulting in severe environmental and ecological damage.
In addition, cuttlebone powder is used in the production of green concrete. It led to the substitution of a portion of cement content, and consequently, this type of concrete causes less harm to environment [128].

4.2. Nacre

Nacre (mother-of-pearl), the inner lustrous and iridescent layer of many mollusc shells, is composed of more than 95% aragonite (a crystallographic form of calcium carbonate—CaCO3) and less than 5% of an organic matrix (consisting of proteins, glycoproteins, polysaccharides and lipids) [129,130,131,132], and it possesses a unique combination of remarkable mechanical strength, impact resistance and toughness. The excellent mechanical and biomedically desirable properties of nacre are related to its hierarchical structure and precisely designed organic–inorganic interface [130,132,133,134,135].
The microarchitecture of nacre has been classically illustrated as a lamellar “bricks-and-mortar” arrangement. The basic structural pattern is the assembly of oriented plate-like aragonite crystals with a “brick” (CaCO3 platelets of micron sizes and sub-micron thicknesses) and “mortar” (organic macromolecular component) organization [129,131,136,137,138]. The water present at the nanograin interfaces also contributes to the viscoelastic nature of nacre [129].

4.2.1. Pharmacological Activity and Pharmaceutical Applications

Owing to this apparent simple morphology and peculiar properties, natural nacre has attracted considerable attention of chemists, biologists and material scientists and engineers. The current knowledge on microstructure and mechanics of nacre has favoured the fabrication of nacre-inspired artificial and related materials. The design and fabrication of de novo synthetic materials is an active area of research in mechanics of materials. A strong emphasis is given on the latest advances on the synthetic design and production of nacre-inspired materials and coatings, to be used in biomedical applications [130,135,137,139,140,141,142], and biomimetic strategies have been proposed to produce new layered nanocomposites in such a way that they produce the best result when interacting with the body [137,143,144,145]. For instance, artificial nacre-like coatings have been fashioned in a layer-by-layer approach using a lamination process. Several different methods have emerged to produce thin layer structures to enhance the mechanical behaviour of the individual components [146,147]. In addition, nacre is widely used as a system model to study biomineralization mechanisms [148,149], and in the future, nacre may have broad applications in biomineralization.
All of this demonstrates how nacre and nacre-derived materials show good interaction with bone, which makes this material attractive in the biomedical field, namely in the orthopaedic or dental areas. The field of bone tissue engineering requires materials capable of providing enhanced mechanical properties and promoting osteogenic cell lineage commitment. While bone repair has long relied almost exclusively on inorganic, calcium phosphate ceramics such as hydroxyapatite and their composites or on non-degradable metals, the organically derived shell nacre generated by molluscs has emerged as a promising alternative [131,132]. Studies, both in vitro and in vivo, have demonstrated nacre’s biocompatibility, biodegradability and osteogenic potential [142].
Nacre powder has a proliferation effect on osteoblasts, osteoclasts and bone marrow cells in the process of bone tissue formation and morphogenesis [142,150]. Nacre contains certain bone remodelling factors that activate osteoblasts and regulate protein signalling transduction to promote osteoblast mineralization [151], and one or more signal molecules capable of activating osteogenic bone marrow cells [152,153]. Likewise, nacre is well tolerated by the host tissue and stimulates a faster osteogenesis [154,155,156].
Nacre can be used directly as a bulk implant or as part of a composite material when combined with polymers or other ceramic products [131,132]. In vivo studies have shown that new bone is formed without causing any inflammation when nacre is implanted in the bone [157,158].
Bivalvia-derived nacre has recently gained interest as a potential alternative ceramic material in orthopaedic biomaterials, combining the integration and mechanical capabilities of calcium phosphates with increased bioactivity derived from proteins and biomolecules [131,132]. The potential of nacre as a versatile, bioactive ceramic capable of improving bone tissue regeneration and will elicit increased research efforts and innovation utilizing nacre.
Furthermore, in vitro studies have shown that water-soluble components extracted from the nacre promote the differentiation of preosteoblast cells and matrix mineralization [159]. Among the molecules that regulate the formation of nacre, p10 and p60 proteins promote these processes [160].
It was shown that nacre itself integrates well into bone tissue [161] and may stimulate the differentiation of stem cells into the osteoblast lineage [162,163]. The scientific basis of fusion with bone was first discovered in 1992 by Lopez et al. [164] and later confirmed by Lamghari et al. [165]. Under closer scrutiny, nacre was found to activate skeletal cells, induce bone formation and provide structural support in a human clinical trial [165]. The “water soluble matrix fraction” of nacre, despite the controversy concerning its definition according to nacre researchers, directly induces the formation of new bone [162]. Molecules from nacre matrix have been shown to decrease bone resorption by restricting osteoclast metabolism [151]. Furthermore, due to its organic content and plate-like design, nacre is mechanically tough, non-immunogenic and rapidly biodegradable, without eliciting detrimental physiological effects. These characteristics of nacre provides a unique substrate for delivery of a functional agent to sites of bone loss in quantities that lead to rapid bone repair and regeneration [132].
Nacre is a promising biomaterial in maxillofacial surgery [166]. Nacre has been proposed as a resorbable and osteoconductive material favouring bone apposition without triggering an inflammatory reaction [166], and it is biocompatible, non-toxic and biodegradable [131,156,166].
Nacre enhances tissue growth and bone tissue bonding. It also has excellent mechanical properties, such as resistance to fracture, that are like those of human bones [156,167]. Nacre powder combined with polylactic acid scaffolds could promote mouse bone marrow mesenchymal stem cell proliferation and increase alkaline phosphatase activity [142]. In the presence of a nacre extract, which can induce the early calcium precipitation in cells (after 7 days), the expression levels of osteogenic markers are higher than in normal with a dose-dependent manner [149]. Nacre extract is likely to stimulate MC3T3-E1 and osteoarthritic osteoblasts in vitro through containing ethanol-soluble diffusible factors. Thus, nacre extract can induce mineralization in osteoblasts [149,158]. However, no in vivo experimentations have been conducted owing possibly to the immunogenic properties of nacre.
In addition to the induction of bone formation, nacre powder promotes skin wound healing. In rat skin incisional injury models, nacre implanted in the dermis increased collagen synthesis by stimulating dermal fibroblasts [168]. Water-soluble nacre, with superior biocompatibility to it, enhanced wound healing recovery properties for burn-induced apoptotic and necrotic cellular damage and spurred angiogenesis [169]. When water-soluble nacre is applied to a burned area, the burn-induced granulation sites are rapidly filled with collagen, and the damaged dermis and epidermis are restored to the appearance of normal skin. Furthermore, water-soluble components from the nacre promote the proliferation of dermal fibroblast cells, enhance collagen secretion [168,169] and improve the healing process of burn wounds by rapidly restoring angiogenesis and fibroblast activity [142].
In several studies aimed at the development of dermatological applications, the in vitro and in vivo results showed that the expression of collagen, essential for healthy maintenance of skin, is increased when nacre is the basis of the treatment [170]. Agarwal et al. [171] found that powdered nacre shows limited cytotoxicity at high concentrations in scar-derived cells and exhibits no apparent oxidative stress on primary skin fibroblast cells and epidermal skin cells. Nacre powder extract induce the reconstruction of intercellular cements in cuticle and can be used to treat dermatitis symptoms [142]. The lipidic constituent of nacre stimulates a reconstitution of the intercellular content of the stratum corneum on atopic dermatitis [172] and moisturizes the skin [170]. For all this, nacre has become an ingredient of interest for skin-related cosmetics.
Correlated with the traditional use of nacre as a sedation and tranquilization agent, anticonvulsant and sedative-hypnotic activities of nacre powder are well known. Nacre original powder, nacre water-soluble protein, nacre acid-soluble protein and nacre conchiolin protein could down-regulate the expression of 5-HT3 receptor and up-regulate the level of GABAB [173].
The administration of nacre extracts improved scopolamine-induced impairment, namely, short-term memory, object recognition and spatial memory [174]. Treatment with nacre extract increases the expression of brain-derived neurotrophic factor and nerve growth factor, which decreased after scopolamine treatment [175].
Water-soluble matrix presents antioxidant activity. It has free radical scavenging ability and inhibits lipid peroxidation [142,159].

4.2.2. Environmental Utilization

Since the excessive petroleum-based plastics entails a great threat to the environment and human health, it is highly desirable to develop new materials for plastic replacement. Inspired by a brick-and-mortar microstructure of nacre, nacre-mimetic sustainable structural materials are being manufactured [176].

5. Documentary Sources Selection Procedures

The immeasurability and dispersion of therapeutic resources throughout history generates a complex data universe. Hence to access the maximum number of documentary sources, a narrative qualitative systematic review of the most important international and national databases was conducted. Thus, in the first step, the query was made in the collection of bibliographic reference databases of Web of Science (1900–present). The survey included the three main areas of research: the Science Citation Index (SCI), the Social Sciences Citation Index (SSCI) and the Arts and Humanities Citation Index (A&HCI). The Cambridge Digital Library and the Anthropology Plus and JSTOR III—Arts and Sciences international databases were consulted. The national resources referenced include the database of Ph.D. Theses, TESEO; the information system of the databases of the CSIC (Spanish Research Council); the Dialnet bibliographic website; Google Scholar; and the catalogue of Public State Libraries. The overall search pattern covered the title, abstract and keywords concerning ethnozoology-related disciplines that have UNESCO codes (e.g., anthropology, the history of medicine, zoology) and the terms marine molluscs, seashells, shells, cuttlebone, cuttlefish bone, nacre, mother-of-pearl, folk medicine, folklore, ethnobiology, ethnozoology, ethnomedicine and zootherapy, in conjunction with the Spanish geographical context. No restrictions regarding the language of the publications consulted, although most relevant studies were published in Spanish. Finally, we have consulted the collections of the Historical Library of the University of Cadiz and its portal dedicated to the conservation of historical heritage, as well as the heritage collections of the Complutense Library of Madrid.
In addition, it should be noted that the humanistic work presented delves into biological taxonomy and animal species identification. Thus, after performing a thorough analysis of the references retrieved and studied, the data were included in a database with several fields to characterise the animal species used, the disease or condition treated, the geographical location of the remedy and its corresponding bibliographic citation. The vernacular names found were contrasted and subjected to discriminatory analysis following biological, ecological and biogeographical criteria. Regarding animal taxonomy and nomenclature, we followed the checklists included in the Catalogue of Life: COL (https://www.catalogueoflife.org/; accessed on 3 August 2023) and the World Register of Marine Species: WoRMS (https://www.marinespecies.org/; accessed on 29 July 2023).

6. Final Considerations and Reflections

As can be seen, the chosen material and method is in line with emerging paradigms where the interdisciplinary or multidisciplinary are giving way to the transdisciplinary through the humanities. In this sense, our work is positioned through discursive analysis from the ethnographic to the historical field to shed light on a biomedical issue related to the search for pharmaceutical resources.
Remedies based on marine animals have been little studied and almost all relegated to the world of curiosities. However, many of these resources, which may seem unusual in our European context, have survived through time, and can inspire ethnopharmacological works.
In addition, consider the importance of historical parallels and fluctuations between different medical systems. Hence our work also wishes to inspire new lines of work based on the identification of species at times when official medicine entered in the biological paradigm.
The work presented reveals the rich history of marine shells and cuttlebones through medicine and science. Moreover, the narrative used documents the evolution of popular and scientific knowledge linked to highly topical cultural and social aspects. We emphasise that these cultural patterns must be analysed and studied with a transdisciplinary approach, opening up new ways of understanding knowledge and science in a broad sense, that can solve global health and environmental problems, and contribute to the fulfilment of Sustainable Development Goals (SDG).
On the other hand, and from a pharmacological point of view, it can be confirmed that the relationship between the chemical composition of these animal derivative products and their medicinal properties is mainly due to the presence of calcium carbonate. For example, the use of this common substance as toothpaste allows the treatment of dental problems. By its physical action on the gums, which increases gingival irrigation, it promotes healing in the case of wounds and/or bleeding. There is no doubt that the cleansing and exfoliating action of calcium carbonate justifies many of its medical applications, which would not be without risk if not managed properly.
Among the documentation consulted, the influence of certain chemical principles in the preparation of remedies was observed. In this respect, we would like to highlight the use of ashes, since the combustion of calcium carbonate (CaCO3) gives rise to calcium oxide (CaO), which is transformed by hydration into calcium hydroxide (Ca(OH)2). This is why we can find justification for medical prescriptions, such as those used at the Royal College of Surgery of the Cadiz Navy, a cornerstone of the union of medical and surgical studies in Europe. As documented (see Section 3.2), those surgeons prepared and applied a very subtle powder made from seashells in complex prescriptions. The scientific basis of these recipes was discussed in the so-called Observaciones de Juntas Literarias (“Remarks of Literary Meetings”), the manuscripts of which should be reread and analysed. Therefore, at this time of the 275th anniversary of this institution, where different professional competences were brought together, we find it interesting to highlight the importance of philosophical eclecticism in science as a conceptual approach that harmonises theories and ideas derived from different fields in order to generate new ideas.
From our point of view, studies on medicine, pharmacy and society can shed light on the true meaning of natural pharmaceutical matter. A new look at polypharmacy without prejudices and a penchant for science could be useful to counteract negationist or fundamentalist positions. Hence, the history of medicine, anthropology and the humanities in general can be used as a source of inspiration and reflection for scientific progress in subjects such as those with which we are dealing.
It is very interesting that the great treatises of pharmacology, as well as the works prior to the biomedical paradigms, show formulas for the elaboration of medicinal lime hydrolats from seashells. Undoubtedly, the use of calcium salts in cosmetology is also in line with ancient treatises, both for their photoprotective character and for their use in face masks for skin whitening.
In general, we can point out that the pharmacological properties of the calcium carbonate of seashells and cuttlebones allowed a fairly wide effective medical use (e.g., as an antacid, anti-diarrhoea, alexipharmic, anti-gout, cardiac tonic, etc.), whose historical, cultural and anthropological view can open new epistemological paths in research with products of animal origin.

Author Contributions

J.A.G. and J.R.V. contributed equally during the data collection, in the design of the research, in the preparation of the first draft of the manuscript, and in the review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

Data sharing is not applicable.

Acknowledgments

We wish to thank several anonymous contributors for their help in improving the manuscript. We would also like to show our gratitude to Rachel Fell for her professional English technical support.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Barandiarán, J.M.; Manterola, A. (Eds.) Medicina Popular en Vasconia; Instituto Labayru–Etniker Euskalerria: Bilbao, Spain, 2004. [Google Scholar]
  2. Luján Navas, A.L. Aprovechamiento y Gestión de Recursos Malacológicos Marinos en la Fachada Mediterránea de la Península Ibérica Durante la Prehistoria Reciente. Ph.D. Thesis, Universidad de Alicante, Alicante, Spain, 2016. [Google Scholar]
  3. Pascual Benito, J.L. Les Jovades (Cocentàina). Notes per a l’estudi del poblament eneolitic a la conca de Riu d’Alcoi. In Actas del Coloquio “El Eneolítico en el País Valenciano”; Instituto de Estatuto “Juan Gil-Albert”: Alcoy, Spain, 1984; pp. 73–79. [Google Scholar]
  4. Batista, C. El marisqueo en la Prehistoria de Gran Canaria. Vector Plus 2001, 18, 67–76. [Google Scholar]
  5. Voultsiadou, E. Therapeutic properties and uses of marine invertebrates in the ancient Greek world and early Byzantium. J. Ethnopharmacol. 2010, 130, 237–247. [Google Scholar] [CrossRef] [PubMed]
  6. Storm Hindley, K. Textual Magic: Charms and Written Amulets in Medieval England; The University of Chicago Press: Chicago, IL, USA, 2023. [Google Scholar]
  7. Hildburgh, W.L. Notes on Spanish amulets. Folklore 1906, 17, 454–471. [Google Scholar] [CrossRef]
  8. Mariño Ferro, X.R. El Simbolismo Animal: Creencias y Significados en la Cultura Occidental; Ediciones Encuentro: Madrid, Spain, 1996. [Google Scholar]
  9. Impelluso, L. La Naturaleza y sus Símbolos: Plantas, Flores y Animales; Electa: Barcelona, Spain, 2003. [Google Scholar]
  10. Ronnberg, A.; Martin, K. (Eds.) El Libro de los Símbolos. Reflexiones Sobre las Imágenes Arquetípicas; Taschen: Köln, Germany, 2011. [Google Scholar]
  11. Biedermann, H. Diccionario de Símbolos; Paidós: Barcelona, Spain, 2013. [Google Scholar]
  12. Sánchez Pérez, J.A. Supersticiones Españolas; Saeta: Madrid, Spain, 1948. [Google Scholar]
  13. Moreta Lara, M.A.; Álvarez Curiel, F. Supersticiones Populares Andaluzas; Arguval: Málaga, Spain, 1993. [Google Scholar]
  14. Guichot y Sierra, A. Supersticiones populares recogidas en Andalucía y comparadas con las portuguesas. In Biblioteca de las Tradiciones Populares Españolas, Tomo I; Machado Álvarez, A., Dir.; Francisco Álvarez y Cª Editores: Sevilla, Spain, 1883; pp. 201–300. [Google Scholar]
  15. Domínguez Moreno, J.M. La lactancia en la alta Extremadura. Rev. Folk. 1988, 89, 147–157. [Google Scholar]
  16. Quintía Pereira, R. Cornos, cairos, pezuños e outros amuletos de orixe animal. Galicia Encantada 2010. Available online: http://www.galiciaencantada.com/lenda.asp?cat=17&id=1662 (accessed on 18 April 2023).
  17. A Chave. Os Nomes Galegos dos Moluscos; A Chave: Xinzo de Limia, Spain, 2020; Available online: https://achave.gal/wp-content/uploads/achave_osnomesgalegosdos_moluscos_2020.pdf (accessed on 8 June 2023).
  18. González, J.A.; Amich, F.; Postigo-Mota, S.; Vallejo, J.R. Therapeutic and prophylactic uses of invertebrates in contemporary Spanish ethnoveterinary medicine. J. Ethnobiol. Ethnomed. 2016, 12, 36. [Google Scholar] [CrossRef]
  19. de Arribas y Sánchez, C. A Través de las Islas Canarias; Ed. A. Delgado Yumar: Santa Cruz de Tenerife, Spain, 1900. [Google Scholar]
  20. Ojeda Guerra, A.; Martín Hernández, R. Remedios oftalmológicos populares de la tradición oral de Tenerife y La Palma. Arch. Soc. Canar. Oftalmol. 1976, 1, 89–94. [Google Scholar]
  21. Álvarez Peña, A. Melecina Máxico-Tradicional n’Asturies; VTP Editorial: Gijón, Spain, 2004. [Google Scholar]
  22. Alemany, S.; Francès, L.; Subirós, R. Recull de remeis tradicionals als pobles pescadors de la Costa Brava. Rev. Etnol. Catalunya 2010, 36, 151–154. [Google Scholar]
  23. Otero Fernández, J.M. Medicina popular en La Siberia. Alminar Rev. Cultura 1983, 44, 6. [Google Scholar]
  24. González Pozuelo, F. Rasgos culturales de la sociedad tradicional extremeña. Cuad. Realid. Soc. 1985, 25–26, 85–110. [Google Scholar]
  25. Domínguez Moreno, J.M. Dermatología popular en Extremadura (y IV) granos. Rev. Folk. 2005, 297, 88–97. [Google Scholar]
  26. Castillo de Lucas, A. Folkmedicina; Dossat: Madrid, Spain, 1958. [Google Scholar]
  27. Pérez Vidal, J. Contribución al Estudio de la Medicina Popular Canaria; Ediciones IDEA: Santa Cruz de Tenerife, Spain, 2007. [Google Scholar]
  28. Rodríguez Aguado, O. Un acercamiento a la medicina popular en Ubrique (1996–1997). Cult. Cuid. 2001, 10, 46–62. [Google Scholar] [CrossRef][Green Version]
  29. Gregori, M.P. Medicina Popular en Valencia del Mombuey. Ph.D. Thesis, Universidad de Extremadura, Badajoz, Spain, 2006. [Google Scholar]
  30. Alcántara Montiel, J.F. La Medicina Popular en la Comarca del Alto Guadalhorce; Diputación Provincial de Málaga: Málaga, Spain, 1990. [Google Scholar]
  31. Vokou, D.; Katradi, K.; Kokkini, S. Ethnobotanical survey of Zagori (Epirus, Greece), a renewed centre of folk medicine in the past. J. Ethnopharmacol. 1993, 39, 187–196. [Google Scholar] [CrossRef] [PubMed]
  32. Rich, T.C.G.; Lambrick, C.R.; McNab, C. Conservation of Britain’s biodiversity: Salvia pratensis L. (Lamiaceae), Meadow Clary. Watsonia 1999, 22, 405–411. [Google Scholar]
  33. Khouchlaa, A.; Et-Touys, A.; Lakhdar, F.; Lakhdar, F.E.; El Idrissi, A.E.Y.; Zaakour, F. Ethnomedicinal use, phytochemistry, pharmacology, and toxicology of Salvia verbenaca L.: A review. Biointerface Res. Appl. Chem. 2022, 12, 1437–1469. [Google Scholar]
  34. Alfayate, M.C.; Barrera, I.; Ron, E.; García Jiménez, R.; Pajarón, S.; Pérez-Alonso, M.J. La mixocarpia de Salvia aegyptiaca L. y su aplicación etnobotánica. Bot. Complut. 2008, 32, 213–216. [Google Scholar]
  35. González, J.A.; García-Barriuso, M.; Amich, F. Ethnobotanical study of medicinal plants traditionally used in the Arribes del Duero, western Spain. J. Ethnopharmacol. 2010, 131, 343–355. [Google Scholar] [CrossRef]
  36. López Cano, E. Supersticiones y creencias populares. Alminar Rev. Cultura 1984, 51, 5. [Google Scholar]
  37. Vallejo, J.R.; Peral, D.; Carrasco, M.C. Catálogo de Remedios de la Medicina Popular de Guadiana del Caudillo; Excmo. Ayuntamiento de Guadiana del Caudillo: Guadiana del Caudillo, Spain, 2008. [Google Scholar]
  38. Tejerina Gallardo, A. Usos y Saberes Sobre las Plantas de Monfragüe. Etnobotánica de la Comarca Natural; Itomonfragüe: Cáceres, Spain, 2010. [Google Scholar]
  39. Gordón, F. La Medicina Popular en Valencia del Ventoso. Ph.D. Thesis, Universidad de Extremadura, Badajoz, Spain, 2015. [Google Scholar]
  40. Gandía Hernández, E. Cuidados de la salud en el ámbito familiar y doméstico: Un rol de género. Remedios tradicionales usados en Villena (Alicante). Feminismo/s 2007, 10, 31–47. [Google Scholar] [CrossRef][Green Version]
  41. García Arambilet, L.A. Medicina Popular en la Provincia de Soria: Descripción y Análisis de sus Prácticas. Ph.D. Thesis, Universidad de Salamanca, Salamanca, Spain, 1990. [Google Scholar]
  42. Hualde Pascual, C.; Ormazábal Herraiz, A. Usos y prácticas de medicina y veterinaria popular en la Campiña de Guadalajara. Cuad. Etnol. Guadalaj. 2002, 34, 273–306. [Google Scholar]
  43. Vallejo, J.R.; González, J.A. The medical use of leeches in contemporary Spain: Between science and tradition. Acta Med.-Hist. Adriat. AMHA 2015, 13, 131–158. [Google Scholar]
  44. Bazaliński, D.; Kózka, M.; Karnas, M.; Więch, P. Effectiveness of chronic wound debridement with the use of larvae of Lucilia sericata. J. Clin. Med. 2019, 8, 1845. [Google Scholar] [CrossRef]
  45. Barriola, I.M. La Medicina Popular en el País Vasco; Biblioteca Vascongada de los Amigos del País: San Sebastián, Spain, 1952. [Google Scholar]
  46. Erkoreka, A. La medicina popular en el País Vasco. Anthropologica 1987, 1, 63–75. [Google Scholar]
  47. López Ruiz, J. Instrumentos complementarios de los cuidados enfermeros: Toma de posición. Enferm. Clin. 2003, 13, 227–236. [Google Scholar] [CrossRef]
  48. Grupo de Terapias Complementarias del Colegio Oficial de Enfermería de Barcelona (GTC-COE Barcelona). Instrumentos Complementarios de los Cuidados de Enfermería—Documento Marco; COIB: Barcelona, Spain, 2004. [Google Scholar]
  49. Perdiguero, E.; Comelles, J.M. El estudio del pluralismo médico en España: Una aproximación histórica. In Pluralismo Médico y Curas Alternativas; Cuadrada, C., Ed.; Publicacions Universitat Rovira i Virgili: Tarragona, Spain, 2020; pp. 7–50. [Google Scholar]
  50. Perdiguero, E.; Comelles, J.M. Cultura, salud y enfermedad: Una medicina plural. In Manual de Historia de la Medicina; Barona Vilar, J.L., Coord.; Tirant lo Blanch: Valencia, Spain, 2023; pp. 53–64. [Google Scholar]
  51. Brondizio, E.S.; O’Brien, K.; Bai, X.; Biermann, F.; Steffen, W.; Berkhout, F.; Cudennec, C.; Lemos, M.C.; Wolfe, A.; Palma-Oliveira, J.; et al. Re-Conceptualizing the Anthropocene: A Call for Collaboration. Glob. Environ. Chang. 2016, 39, 318–327. [Google Scholar] [CrossRef]
  52. Kitch, S.L. How Can Humanities Interventions Promote Progress in the Environmental Sciences? Humanities 2017, 6, 76. [Google Scholar] [CrossRef]
  53. García, V.M. Dioscórides: Plantas y Remedios Medicinales (De Materia Medica). Libros I–III; Gredos: Madrid, Spain, 1998. [Google Scholar]
  54. López Eire, A. Dioscórides Interactivo Sobre los Remedios Medicinales—Manuscrito de Salamanca; Project MICINN HUM-2006-08794; Ediciones Universidad de Salamanca: Salamanca, Spain, 2006; Available online: https://dioscorides.usal.es/ (accessed on 8 May 2023).
  55. Laguna, A. Dioscórides P. Acerca de la Materia Medicinal… Salamanca. Traducción y Comentarios de Andrés Laguna; 1566 (facsimile edition); MRA: Barcelona, Spain, 1994. [Google Scholar]
  56. Cantó, J.; Gómez Santamaría, I.; González Marín, S.; Tarriño, E. Plinio: Historia Natural, 2nd ed.; Cátedra: Madrid, Spain, 2007. [Google Scholar]
  57. Valledor de Lozoya, A.; Araujo, R. How the naiad was drawn: A pre-Linnean iconography of freshwater mussels. Malacologia 2011, 53, 381–402. [Google Scholar] [CrossRef]
  58. Viñayo González, A.; Riesco Álvarez, H.B. Hortus Sanitatis, de Avibus, de Piscibus; facsimile ed.; Ediciones de la Universidad de León: León, Spain, 1998. [Google Scholar]
  59. Betlloch-Mas, I.; Chiner, E.; Chiner-Betlloch, J.; Llorca-Ibi, F.X.; Martín-Pascual, L. The use of animals in medicine of Latin tradition: Study of the Tresor de Beutat, a medieval treatise devoted to female cosmetics. J. Ethnobiol. Tradit. Med. Photon 2014, 121, 752–760. [Google Scholar]
  60. Ruiz Bravo-Villasante, C. Libro de las Utilidades Animales; Fundación Universitaria Española: Madrid, Spain, 1980. [Google Scholar]
  61. Dorveaux, P. L’antidotaire Nicolas. Deux Traductions Françaises de l’Antidotarium Nicolai. L’une du XIVè Siècle Suivie de Quelques Recettes de la Même Époque et d’un Glossaire. L’autre du XVè Siècle Incomplète. Publiées D’après les Manuscrits Français 25327 et 14827 de la Bibliothèque Nationale; H. Welter: Paris, France, 1896. [Google Scholar]
  62. Dorveaux, P. Antidotarium Nicolai; BiblioBazaar: Charleston, SC, USA, 2010. [Google Scholar]
  63. Vallejo, J.R.; Cobos, J.M. El recetario de la Escuela de Salerno conocido como el “Antidotarium Nicolai”. Med. Natur. 2013, 7, 35–41. [Google Scholar]
  64. Castell, F.A. Theorica y Pratica de Boticarios en que se Trata de la arte y Forma como se han de Componer las Confectiones Ansi Interiores Como Exteriores; Sebastian de Cormellas: Barcelona, Spain, 1592. [Google Scholar]
  65. Pensado, J.L. (Ed.) Colección de Voces y Frases Gallegas (De Fr. Martín Sarmiento); Ediciones Universidad de Salamanca: Salamanca, Spain, 1970. [Google Scholar]
  66. Vallejo, J.R.; Cobos, J.M. De la botánica médica a la Farmacia en España: La obra de Pedro Benedicto Mateo. Med. Natur. 2015, 9, 82–87. [Google Scholar]
  67. Saladino, F. Compendium Aromatariorum. … Saladino: [comie[n]ça el co[m]pendio de los Boticarios/Compuesto por el dotor Saladino…; Trasladado del latin en Lengua Vulgar Castellana por el lice[n]ciado Alfonso Rodriguez de Tudela]; Arnao Guillen de Brocar: Valladolid, Spain, 1515. [Google Scholar]
  68. Francés Causapé, M.C. Consideraciones Sobre Creencias, Farmacia y Terapéutica; Instituto de España—Real Academia Nacional de Farmacia, Discursos de la RANF: Madrid, Spain, 2009. [Google Scholar]
  69. Croll, O. La Royale Chymie de Crollius, Traduitte en François, par J. Marcel de Boulene; Pierre Drobet: Lyon, France, 1627. [Google Scholar]
  70. Costa-Neto, E.M. Os moluscos na zooterapia: Medicina tradicional e importância clínico-farmacológica. Biotemas 2006, 19, 71–78. [Google Scholar]
  71. Laval, E. Botica de los Jesuitas de Santiago; Asociación Chilena de Asistencia Social: Santiago, Chile, 1953. [Google Scholar]
  72. Fresquet Febrer, J.L. El uso de productos del reino mineral en la terapéutica del siglo XVI. El libro de los Medicamentos simples de Juan Fragoso (1581) y el Antidotario de Juan Calvo (1580). Asclepio 1999, 51, 55–92. [Google Scholar] [CrossRef] [PubMed]
  73. Osorio Oliveros, M.E. Curar el Alma y Medicar el Cuerpo: Ciencia Médica Jesuita en el Nuevo Reino de Granada (XVII–XVIII). El caso de la Botica del Colegio Máximo de Santafé. Ph.D. Thesis, Universidad de los Andes, Bogotá, Colombia, 2011. [Google Scholar]
  74. Bustos Rodríguez, M. Los Cirujanos del Real Colegio de Cádiz en la Encrucijada de la Ilustración (1740–1796); Universidad de Cádiz: Cádiz, Spain, 1983. [Google Scholar]
  75. Clavijo y Clavijo, S. Historia del Cuerpo de Sanidad Militar de la Armada (Génesis; Perspectiva de Siglos; Ruta de Libertad; Sus Celebridades); Tipografía de Fernando Espín: San Fernando, Spain, 1925. [Google Scholar]
  76. Laín Entralgo, P. (Ed.) Historia Universal de la Medicina; Salvat: Barcelona, Spain, 1971–1975. [Google Scholar]
  77. Granjel, L.S. Historia General de la Medicina Española; Ediciones Universidad de Salamanca: Salamanca, Spain, 1978–1986. [Google Scholar]
  78. Ferrer, D. Historia del Real Colegio de Cirugía de la Armada de Cádiz, 2nd ed.; Universidad de Cádiz: Cádiz, Spain, 1983. [Google Scholar]
  79. Cabrera Afonso, J.R. La Medicina española del siglo XVIII: El Real Colegio de Cirugía de Cádiz. Real Acad. Nac. Med. 2008, 4, 581–606. [Google Scholar]
  80. Redruello-Guerrero, P. Los Reales Colegios de Cirugía de Barcelona y Madrid en el siglo XVIII. Actual Med. 2020, 105, 202–208. [Google Scholar] [CrossRef]
  81. de Vega, L. Pharmacopea de la Armada o Real Catálogo de Medicamentos Pertenecientes a las Enfermedades Medicas…; Imp. D. Manuel Ximenez Carreño: Cádiz, Spain, 1759. [Google Scholar]
  82. Márquez Espinos, C. Las Juntas Literarias del Real Colegio de Cirugía; Universidad de Cádiz: Cádiz, Spain, 1986. [Google Scholar]
  83. Orozco Acuaviva, A. El modelo de Enseñanza en el Real Colegio de Cirugía de Cádiz en el siglo XVIII. Gades 1988, 18, 87–108. [Google Scholar]
  84. Cabrera Afonso, J.R. El libro Médico-Quirúrgico de los Reales Colegios de Cirugía Españoles en la Ilustración; Servicio de Publicaciones de la Universidad de Cádiz: Cádiz, Spain, 1990. [Google Scholar]
  85. Gestido del Olmo, M.R. Los Fondos Bibliográficos y Humanísticos del Real Colegio de Cirugía de Cádiz. Catalogación y Estudio Crítico. Cádiz.-(1994): Una Biblioteca Ilustrada Gaditana. Los Fondos Bibliográficos Humanísticos del Real Colegio de Cirugía de la Armada; Universidad de Cádiz: Cádiz, Spain, 1991. [Google Scholar]
  86. Remón Rodríguez, A. El Libro Médico-Científico en la Biblioteca del Real Colegio de Cirugía de Cádiz (1748–1844); Universidad de Cádiz: Cádiz, Spain, 2017. [Google Scholar]
  87. Pérez Pérez, A.; Vallejo, J.R. The smallpox vaccine in Latin America: A new approach (1801–1804). Medicina 2023, 59, 1093. [Google Scholar] [CrossRef]
  88. Mercant Ramírez, J. Historia de la Farmacoterapia: Siglos XVIII y XIX. La Farmacia Monástica de la Real Cartuja de Valldemossa; Universitat Autònoma de Barcelona: Barcelona, Spain, 2009. [Google Scholar]
  89. Archivo de la Facultad de Medicina de Cádiz (AFMC). Registro 8353, Libro de Cuentas del Real Colegio de Cirugía de Cádiz que Tiene Principio en año de 1751. Tomo 1º (1751–1780), f. 27; Facultad de Medicina—Universidad de Cádiz: Cádiz, Spain, 1751–1780. [Google Scholar]
  90. Ruiz Vega, P. La farmacia en la Real Academia de Medicina y Cirugía de Cádiz (Siglo XIX). Ph.D. Thesis, Universidad de Cádiz, Cádiz, Spain, 2016. [Google Scholar]
  91. Álvarez Alcalá, F. Formulario Universal o Guía Práctica del Médico, del Cirujano y del Farmacéutico; Librería de Don Ángel Calleja: Madrid, Spain, 1850. [Google Scholar]
  92. Nysten, P.H. Diccionario de Medicina, Cirugía, Farmacia, Medicina Legal, Física, Química, Botánica, Mineralogía, Zoología y Veterinaria: Por P. H. Nysten, Sucesivamente Aumentado […] por Bricheteau [et al. …]. Traducido Libremente al Castellano por José Castells; Imprenta de J. Roger: Barcelona, Spain, 1848. [Google Scholar]
  93. Gómez Pamo, J.R. Elementos de Materia Farmacéutica Mineral, Animal y Vegetal; Moya y Plaza: Madrid, Spain, 1871. [Google Scholar]
  94. Benkendorff, K. Molluscan biological and chemical diversity: Secondary metabolites and medicinal resources produced by marine molluscs. Biol. Rev. 2010, 85, 757–775. [Google Scholar] [CrossRef]
  95. Leal, M.C.; Madeira, C.; Brandão, C.A.; Puga, J.; Calado, R. Bioprospecting of marine invertebrates for new natural products—A chemical and zoogeographical perspective. Molecules 2012, 17, 9842–9854. [Google Scholar] [CrossRef]
  96. Benkendorff, K.; Rudd, D.; Nongmaithem, B.D.; Liu, L.; Young, F.; Edwards, V.; Ávila, C.; Abbott, C.A. Are the traditional medical uses of Muricidae molluscs substantiated by their pharmacological properties and bioactive compounds? Mar. Drugs 2015, 13, 5237–5275. [Google Scholar] [CrossRef]
  97. Ahmad, T.B.; Liu, L.; Kotiw, M.; Benkendorff, K. Review of anti-inflammatory, immune-modulatory and wound healing properties of molluscs. J. Ethnopharmacol. 2017, 210, 156–178. [Google Scholar] [CrossRef]
  98. Derby, C.D.; Kicklighter, C.E.; Johnson, P.M.; Zhang, X. Chemical composition of inks of diverse marine molluscs suggests convergent chemical defenses. J. Chem. Ecol. 2007, 33, 1105–1113. [Google Scholar] [CrossRef] [PubMed]
  99. Dang, V.T.; Benkendorff, K.; Green, T.; Speck, P. Marine snails and slugs: A great place to look for antiviral drugs. J. Virol. 2015, 89, 8114–8118. [Google Scholar] [CrossRef] [PubMed]
  100. Florek, M.; Fornal, E.; Gómez-Romero, P.; Zieba, E.; Paszkowicz, W.; Lekki, J.; Nowak, J.; Kuczumow, A. Complementary microstructural and chemical analyses of Sepia officinalis endoskeleton. Mater. Sci. Eng. C 2009, 29, 1220–1226. [Google Scholar] [CrossRef]
  101. Cadman, J.; Zhou, S.; Chen, Y.; Li, Q. Cuttlebone: Characterisation, application and development of biomimetic materials. J. Bionic. Eng. 2012, 9, 367–376. [Google Scholar] [CrossRef]
  102. Le Pabic, C.; Marie, A.; Marie, B.; Percot, A.; Bonnaud-Ponticelli, L.; López, P.J.; Luquet, G. First proteomic analyses of the dorsal and ventral parts of the Sepia officinalis cuttlebone. J. Proteom. 2017, 150, 63–73. [Google Scholar] [CrossRef]
  103. North, L.; Labonte, D.; Oyen, M.L.; Coleman, M.P.; Caliskan, H.B.; Johnston, R.E. Interrelated chemical-microstructural-nanomechanical variations in the structural units of the cuttlebone of Sepia officinalis. APL Mater. 2017, 5, 116103. [Google Scholar] [CrossRef]
  104. Sundaram, S. The various uses of cephalopods. Fish. Chimes 2009, 29, 23–25. [Google Scholar]
  105. García-Enríquez, S.; Guadarrama, H.E.; Reyes-González, I.; Mendizábal, E.; Jasso-Gastinel, C.F.; García-Enríquez, B.; Rembao-Boiorquez, D.; Pane-Pianese, C. Mechanical performance and in vivo tests of an acrylic bone cement filled with bioactive Sepia officinalis cuttlebone. J. Biomater. Sci. Polym. Ed. 2010, 21, 113–125. [Google Scholar] [CrossRef]
  106. Curti, F.; Serafim, A.; Olaret, E.; Dinescu, S.; Samoila, I.; Vasile, B.S.; Iovu, H.; Lungu, A.; Stancu, I.C.; Marinescu, R. Development of biocomposite alginate-cuttlebone-gelatin 3D printing inks designed for scaffolds with bone regeneration potential. Mar. Drugs 2022, 20, 670. [Google Scholar] [CrossRef]
  107. Hongmin, L.; Wei, Z.; Xingrong, Y.; Jing, W.; Wenxin, G.; Jihong, C.; Xin, X.; Fulin, C. Osteoinductive nanohydroxyapatite bone substitute prepared via in situ hydrothermal transformation of cuttlefish bone. J. Biomed. Mater. Res. B Appl. Biomater. 2015, 103, 816–824. [Google Scholar] [CrossRef]
  108. Mansouri, K.; Fattahian, H.; Mansouri, N.; Mostafavi, P.G.; Kajbafzadef, A. The role of cuttlebone and cuttlebone derived hydroxyapatite with platelet rich plasma on tibial bone defect healing in rabbit: An experimental study. Kafkas Univ. Vet. Fak. Derg. 2018, 24, 107–115. [Google Scholar] [CrossRef]
  109. Won, S.; Lee, J.M.; Park, H.; Seo, J.; Cheong, J. Evaluation of the bone defect regeneration after implantation with cuttlebone in rabbit. J. Vet. Clin. 2015, 32, 410–416. [Google Scholar] [CrossRef]
  110. Palaveniene, A.; Lebedevaite, M.; Liesiene, J. Alginate capsules with cuttlebone-derived fillers as an integrated solution for bone repair. Mater. Sci. 2018, 24, 295–300. [Google Scholar] [CrossRef]
  111. Palaveniene, A.; Songailiene, K.; Baniukaitiene, O.; Tamburaci, S.; Kimna, C.; Tihminlioglu, F.; Liesiene, J. The effect of biomimetic coating and cuttlebone microparticle reinforcement on the osteoconductive properties of cellulose-based scaffolds. Int. J. Biol. Macromol. 2020, 152, 1194–1204. [Google Scholar] [CrossRef]
  112. Kumar, M.N.V.R.; Muzzarelli, R.A.A.; Muzzarelli, C.; Sashiwa, H.; Domb, A.J. Chitosan chemistry and pharmaceutical perspectives. Chem. Rev. 2004, 104, 6017–6084. [Google Scholar] [CrossRef]
  113. Muzzarelli, R.A.A.; Muzzarelli, C. Chitosan chemistry: Relevance to the biomedical sciences. Adv. Polymer Sci. 2005, 186, 151–209. [Google Scholar]
  114. Rinaudo, M. Chitin and chitosan: Properties and application. Prog. Polymer Sci. 2006, 31, 603–632. [Google Scholar] [CrossRef]
  115. Vino, A.B.; Ramasamy, P.; Shanmugam, V.; Shanmugam, A. Extraction, characterization and in vitro antioxidative potential of chitosan and sulfated chitosan from Cuttlebone of Sepia aculeata Orbigny, 1848. Asian Pac. J. Trop. Biomed. 2012, 2 (Suppl. S1), S334–S341. [Google Scholar] [CrossRef]
  116. Garcinuño, S.; Aranaz, I.; Civera, C.; Arias, C.; Acosta, N. Evaluating non-conventional chitosan sources for controlled release of risperidone. Polymers 2022, 14, 1355. [Google Scholar] [CrossRef]
  117. Karthik, R.; Manigandan, V.; Saravanan, R.; Rajesh, R.P.; Chandrika, B. Structural characterization and in vitro biomedical activities of sulfated chitosan from Sepia pharaonis. Int. J. Biol. Macromol. 2016, 84, 319–328. [Google Scholar] [CrossRef]
  118. Narasimman, V.; Ramachandran, S. In silico analysis of low molecular weight sulfated chitosan from Sepia brevimana as potential inhibitors of white spot syndrome envelope proteins. Biomass Conv. Bioref. 2023. [Google Scholar] [CrossRef]
  119. Shanmugam, A.; Mahalakshmi, T.S.; Barwin, V.A. Antimicrobial activity of polysaccharides isolated from the cuttlebone of Sepia aculeate and Sepia brevimana: An approach to selected antimicrobial activity for human pathogenic microorganisms. J. Fish Aquat. Sci. 2008, 3, 268–274. [Google Scholar]
  120. Yazdanpanah, G.; Javid, N.; Honarmandrad, Z.; Amirmahani, N.; Nasiri, A. Evaluation of antimicrobial activities of powdered cuttlebone against Klebsiella oxytoca, Staphylococcus aureus, and Aspergillus flavus. Environ. Health Eng. Manag. J. 2021, 8, 39–45. [Google Scholar] [CrossRef]
  121. Jang, J.K.; Lee, O.S.; Kang, T.J.; Lim, S.C. Wound healing effect of cuttlebone extract in burn injury of rat. Food Sci. Biotechnol. 2013, 22 (Suppl. S1), 99–105. [Google Scholar] [CrossRef]
  122. Lee, K.M.; Shim, H.; Lee, G.S.; Park, I.H.; Lee, O.S.; Lim, S.C.; Kang, T.J. Chitin from the extract of cuttlebone induces acute inflammation and enhances MMP1 expression. Biomol. Ther. 2013, 21, 246–250. [Google Scholar] [CrossRef][Green Version]
  123. Mostoufi, A.; Bavarsad, N.; Aryanfar, S.; Akhgari, A. New natural marine antacid drug from cuttlebone. Pharm. Sci. 2018, 24, 227–234. [Google Scholar] [CrossRef]
  124. Bettencourt, V.; Guerra, A. Carbon- and oxygen-isotope composition of the cuttlebone of Sepia officinalis: A tool for predicting ecological information? Mar. Biol. 1999, 133, 651–657. [Google Scholar] [CrossRef]
  125. Dance, M.A.; Bello, G.; Furey, N.B.; Rooker, J.R. Species-specific variation in cuttlebone δ13C and δ18O for three species of Mediterranean cuttlefish. Mar. Biol. 2014, 161, 489–494. [Google Scholar] [CrossRef]
  126. Vibhatabandhu, P.; Srithongouthai, S. Removal of copper (II) from aqueous solutions using cuttlebone as bio-adsorbent. App. Envi. Res. 2016, 38, 39–47. [Google Scholar] [CrossRef]
  127. Xu, J.; Che, P.; Zhang, H.; Zhang, Y.; Wu, J.; Li, W.; He, J.; Ma, Z.; Li, T.; Dong, Y.; et al. Superhydrophobic modification of biomass cuttlebone applied to oil spill remediation. Materials 2022, 15, 4401. [Google Scholar] [CrossRef]
  128. Mirzabagheri, S.; Derhamjani, G.; Maharati, S.; Ziaee, Z.; Vatankhah, F.; Mirzabagheri, D. Using cuttlebone powder to produce green concrete. J. Appl. Eng. Sci. 2018, 8, 25–28. [Google Scholar] [CrossRef]
  129. Sun, J.; Bhushan, B. Hierarchical structure and mechanical properties of nacre: A review. RSC Adv. 2012, 2, 7617–7632. [Google Scholar] [CrossRef]
  130. Wang, J.; Cheng, Q.; Tang, Z. Layered nanocomposites inspired by the structure and mechanical properties of nacre. Chem. Soc. Rev. 2012, 41, 1111–1129. [Google Scholar] [CrossRef] [PubMed]
  131. Gerhard, E.M.; Wang, W.; Li, C.; Guo, J.; Ozbolat, I.T.; Rahn, K.M.; Armstrong, A.D.; Xia, J.; Qian, G.; Yang, J. Design strategies and applications of nacre-based biomaterials. Acta Biomater. 2017, 54, 21–34. [Google Scholar] [CrossRef]
  132. Ben-Nissan, B.; Choi, A.H.; Green, D.W. Marine derived biomaterials for bone regeneration and tissue engineering: Learning from nature. In Marine-Derived Biomaterials for Tissue Engineering Applications; Choi, A.H., Ben-Nissan, B., Eds.; Springer Nature Singapore Pte Ltd.: Singapore, 2019; pp. 51–78. [Google Scholar]
  133. Sumitomo, T.; Kakisawa, H.; Owaki, Y.; Kagawa, Y. Transmission electron microscopy observation of nanoscale deformation structures in nacre. J. Mater. Res. 2008, 23, 3213–3221. [Google Scholar] [CrossRef]
  134. Yao, N.; Epstein, A.K.; Liu, W.W.; Sauer, F.; Yang, N. Organic-inorganic interfaces and spiral growth in nacre. J. R. Soc. Interface 2009, 6, 367. [Google Scholar] [CrossRef]
  135. Barthelat, F. Nacre from mollusk shells: A model for high-performance structural materials. Bioinspir. Biomim. 2010, 5, 035001. [Google Scholar] [CrossRef]
  136. Cartwright, J.H.; Checa, A.G. The dynamics of nacre self-assembly. J. R. Soc. Interface 2007, 4, 491–504. [Google Scholar] [CrossRef]
  137. Luz, G.M.; Mano, J.F. Biomimetic design of materials and biomaterials inspired by the structure of nacre. Phil. Trans. R. Soc. A 2009, 367, 1587–1605. [Google Scholar] [CrossRef]
  138. Stempflé, P.; Pantalé, O.; Rousseau, M.; Lopez, E.; Bourrat, X. Mechanical properties of the elemental nanocomponents of nacre structure. Mater. Sci. Eng. C 2010, 30, 715–721. [Google Scholar] [CrossRef]
  139. Sarkar, R.; Banerjee, G. Ceramic based bio-medical implants. Interceram 2010, 59, 98–102. [Google Scholar]
  140. Barthelat, F.; Zhu, D. A novel biomimetic material duplicating the structure and mechanics of natural nacre. J. Mater. Res. 2011, 26, 1203–1215. [Google Scholar] [CrossRef]
  141. Lalzawmliana, V.; Mukherjee, P.; Kundu, B.; Nandi, S.K. Clinical application of biomimetic marine-derived materials for tissue engineering. In Marine-Derived Biomaterials for Tissue Engineering Applications; Choi, A.H., Ben-Nissan, B., Eds.; Springer Nature Singapore Pte Ltd.: Singapore, 2019; pp. 329–356. [Google Scholar]
  142. Pei, J.; Wang, Y.; Zou, X.; Ruan, H.; Tang, C.; Liao, J.; Si, G.; Sun, P. Extraction, purification, bioactivities and application of matrix proteins from pearl powder and nacre powder: A review. Front. Bioeng. Biotechnol. 2021, 9, 649665. [Google Scholar] [CrossRef] [PubMed]
  143. Kobayashi, I.; Samata, T. Bivalve shell structure and organic matrix. Mater. Sci. Eng. C 2006, 6, 692–698. [Google Scholar] [CrossRef]
  144. Corni, I.; Harvey, T.J.; Wharton, J.A.; Stokes, K.R.; Walsh, F.C.; Wood, R.J.K. A review of experimental techniques to produce a nacre-like structure. Bioinspir. Biomim. 2012, 7, 031001. [Google Scholar] [CrossRef] [PubMed]
  145. Bouville, F.; Maire, E.; Meille, S.; Van de Moortèle, B.; Stevenson, A.J.; Deville, S. Strong, tough and brittle bioinspired ceramics from brittle constituents. Nat. Mater. 2014, 13, 508–524. [Google Scholar] [CrossRef]
  146. Tang, Z.; Kotov, N.A.; Magonov, S.; Ozturk, B. Nanostructured artificial nacre. Nat. Mater. 2003, 2, 413–418. [Google Scholar] [CrossRef]
  147. Wei, H.; Ma, N.; Shi, F.; Wang, Z.; Zhang, X. Artificial nacre by alternating preparation of layer-by-layer polymer films and CaCO3 strata. Chem. Mater. 2007, 19, 1974–1978. [Google Scholar] [CrossRef]
  148. Schoeppler, V.; Lemanis, R.; Reich, E.; Pusztai, T.; Gránásy, L.; Zlotnikov, I. Crystal growth kinetics as an architectural constraint on the evolution of molluscan shells. Proc. Natl. Acad. Sci. USA 2019, 116, 20388–20397. [Google Scholar] [CrossRef]
  149. Wan, M.C.; Qin, W.; Lei, C.; Li, Q.H.; Meng, M.; Fang, M.; Song, W.; Chen, J.H.; Tay, F.; Niu, L.N. Biomaterials from the sea: Future building blocks for biomedical applications. Bioact. Mater. 2021, 6, 4255–4285. [Google Scholar] [CrossRef]
  150. Mao, Q.H.; Xu, P. Research progress of pearl/nacre in bone tissue repair. J. Oral Sci. Res. 2016, 32, 311–313. [Google Scholar]
  151. Duplat, D.; Chabadel, A.; Gallet, M.; Berland, S.; Bédouet, L.; Rousseau, M.; Kamel, S.; Milet, C.; Jurdic, P.; Brazier, M.; et al. The in vitro osteoclastic degradation of nacre. Biomaterials 2007, 28, 2155–2162. [Google Scholar] [CrossRef] [PubMed]
  152. Almeida, M.J.; Milet, C.; Peduzzi, J.; Pereira, L.; Haigle, J.; Barthelemy, M.; Lopez, E. Effect of water-soluble matrix fraction extracted from the nacre of Pinctada maxima on the alkaline phosphatase activity of cultured fibroblasts. J. Exp. Zool. 2000, 288, 327–334. [Google Scholar] [CrossRef] [PubMed]
  153. Rousseau, M.; Pereira-Mouries, L.; Almeida, M.J.; Milet, C.; Lopez, E. The water-soluble matrix fraction from the nacre of Pinctada maxima produces earlier mineralization of MC3T3-E1 mouse pre-osteoblasts. Comp. Biochem. Phys. B 2003, 135, 1–7. [Google Scholar] [CrossRef]
  154. Lamghari, M.; Antonietti, P.; Berland, S.; Laurent, A.; Lopez, E. Arthrodesis of lumbar spine transverse processes using nacre in rabbit. J. Bone Miner. Res. 2001, 16, 2232–2237. [Google Scholar] [CrossRef]
  155. Asvanund, P.; Chunhabundit, P.; Suddhasthira, T. Potential induction of bone regeneration by nacre: An in vitro study. Implant Dent. 2011, 20, 32–39. [Google Scholar] [CrossRef]
  156. Zhang, G.; Brion, A.; Willemin, A.S.; Piet, M.H.; Moby, V.; Bianchi, A.; Mainard, D.; Galois, L.; Gillet, P.; Rousseau, M. Nacre, a natural, multi-use, and timely biomaterial for bone graft substitution. J. Biomed. Mater. Res. A 2017, 105, 662–671. [Google Scholar] [CrossRef]
  157. Atlan, G.; Delattre, O.; Berland, S.; LeFaou, A.; Nabias, G.; Cot, D.; Lopez, E. Interface between bone and nacre implants in sheep. Biomaterials 1999, 20, 1017–1022. [Google Scholar] [CrossRef]
  158. Brion, A.; Zhang, G.; Dossot, M.; Moby, V.; Dumas, D.; Hupont, S.; Piet, M.H.; Bianchi, A.; Mainard, D.; Galois, L.; et al. Nacre extract restores the mineralization capacity of subchondral osteoarthritis osteoblasts. J. Struct. Biol. 2015, 192, 500–509. [Google Scholar] [CrossRef]
  159. Chaturvedi, R.; Singha, P.K.; Dey, S. Water soluble bioactives of nacre mediate antioxidant activity and osteoblast differentiation. PLoS ONE 2013, 8, e84584. [Google Scholar] [CrossRef]
  160. Lao, Y.; Zhang, X.; Zhou, J.; Su, W.; Chen, R.; Wang, Y.; Zhou, W.; Xu, Z.F. Characterization and in vitro mineralization function of a soluble protein complex P60 from the nacre of Pinctada fucata. Comp. Biochem. Physiol. B 2007, 148, 201–208. [Google Scholar] [CrossRef] [PubMed]
  161. Berland, S.; Delattre, O.; Borzeix, S.; Catonne, Y.; Lopez, E. Nacre/bone interface changes in durable nacre endosseous implants in sheep. Biomaterials 2005, 26, 2767–2773. [Google Scholar] [CrossRef] [PubMed]
  162. Rousseau, M.; Boulzaguet, H.; Biagianti, J.; Duplat, D.; Milet, C.; Lopez, E.; Bedouet, L. Low molecular weight molecules of oyster nacre induce mineralization of the MC3T3-E1 cells. Biomed. Mater. Res. A 2008, 85, 487–497. [Google Scholar] [CrossRef] [PubMed]
  163. Zhu, L.Q.; Wang, H.M.; Xu, J.H.; Wei, D.; Zhao, W.Q.; Wang, X.X.; Wu, N.P. Effects of titanium implant surface coated with natural nacre on MC3T3E1 cell line in vitro. Prog. Biochem. Biophys. 2008, 35, 671–675. [Google Scholar]
  164. Lopez, E.; Vidal, B.; Berland, S.; Camprasse, S.; Camprasse, G.; Silve, C. Demonstration of the capacity of nacre to induce bone formation by human osteoblasts maintained in vitro. Tissue Cell 1992, 24, 667–679. [Google Scholar] [CrossRef]
  165. Lamghari, M.; Berland, S.; Laurent, A.; Huet, H.; Lopez, E. Bone reactions to nacre injected percutaneously into the vertebrae of sheep. Biomaterials 2001, 22, 555–562. [Google Scholar] [CrossRef]
  166. Kün-Darbois, J.D.; Libouban, H.; Camprasse, G.; Camprasse, S.; Chappard, D. In vivo osseointegration and erosion of nacre screws in an animal model. J. Biomed. Mater. Res. B 2021, 109, 780–788. [Google Scholar] [CrossRef]
  167. Song, F.; Soh, A.K.; Bai, Y.L. Structural and mechanical properties of the organic matrix layers of nacre. Biomaterials 2003, 24, 3623–3631. [Google Scholar] [CrossRef]
  168. Lopez, E.; Le Faou, A.; Borzeix, S.; Berland, S. Stimulation of rat cutaneous fibroblasts and their synthetic activity by implants of powdered nacre (mother of pearl). Tissue Cell 2000, 32, 95–101. [Google Scholar] [CrossRef]
  169. Lee, K.; Kim, H.; Kim, J.M.; Chung, Y.H.; Lee, T.Y.; Lim, H.S.; Lim, J.H.; Kim, T.; Bae, J.S.; Woo, C.H.; et al. Nacre-driven water-soluble factors promote wound healing of the deep burn porcine skin by recovering angiogenesis and fibroblast function. Mol. Biol. Rep. 2012, 39, 3211–3218. [Google Scholar] [CrossRef]
  170. Santhana Vignesh, T.; Suja, C.P. Marine molluscan shell for dermal regeneration: A review. Pro. Aqua Farm. Mar. Biol. 2019, 2, 180025. [Google Scholar]
  171. Agarwal, V.; Tjandra, E.S.; Iyer, K.S.; Humfrey, B.; Fear, M.; Wood, F.M.; Dunlop, S.; Raston, C.L. Evaluating the effects of nacre on human skin and scar cells in culture. Toxicol. Res. 2014, 3, 223–227. [Google Scholar] [CrossRef]
  172. Rousseau, M.; Bedouet, L.; Lati, E.; Gasser, P.; Le Ny, K.; Lopez, E. Restoration of stratum corneum with nacre lipids. Comp. Biochem. Physiol. Part B Biochem. Mol. Biol. 2006, 145, 1–9. [Google Scholar] [CrossRef]
  173. Zhang, J.X.; Li, S.R.; Yao, S.; Bi, Q.R.; Hou, J.J.; Cai, L.Y.; Han, S.M.; Wu, W.Y.; Guo, D.A. Anticonvulsant and sedative-hypnotic activity screening of pearl and nacre (mother of pearl). J. Ethnopharmacol. 2016, 181, 229–235. [Google Scholar] [CrossRef]
  174. Fuji, T.; Inoue, T.; Hasegawa, Y. Nacre extract prevents scopolamine-induced memory deficits in rodents. Asian Pac. J. Trop. Med. 2018, 11, 202–208. [Google Scholar]
  175. Yamagami, H.; Fuji, T.; Wako, M.; Hasegawa, Y. Sulfated polysaccharide isolated from the nacre of pearl oyster improves scopolamine-induced memory impairment. Antioxidants 2021, 10, 505. [Google Scholar] [CrossRef] [PubMed]
  176. Guan, Q.F.; Yang, H.B.; Han, Z.M.; Ling, Z.C.; Yu, S.H. An all-natural bioinspired structural material for plastic replacement. Nat. Commun. 2020, 11, 5401. [Google Scholar] [CrossRef]
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