Therapeutic Potential and Nutraceutical Profiling of North Bornean Seaweeds: A Review

Malaysia has a long coastline surrounded by various islands, including North Borneo, that provide a suitable environment for the growth of diverse species of seaweeds. Some of the important North Bornean seaweed species are Kappaphycus alvarezii, Eucheuma denticulatum, Halymenia durvillaei (Rhodophyta), Caulerpa lentillifera, Caulerpa racemosa (Chlorophyta), Dictyota dichotoma and Sargassum polycystum (Ochrophyta). This review aims to highlight the therapeutic potential of North Bornean seaweeds and their nutraceutical profiling. North Bornean seaweeds have demonstrated anti-inflammatory, antioxidant, antimicrobial, anticancer, cardiovascular protective, neuroprotective, renal protective and hepatic protective potentials. The protective roles of the seaweeds might be due to the presence of a wide variety of nutraceuticals, including phthalic anhydride, 3,4-ethylenedioxythiophene, 2-pentylthiophene, furoic acid (K. alvarezii), eicosapentaenoic acid, palmitoleic acid, fucoxanthin, β-carotene (E. denticulatum), eucalyptol, oleic acid, dodecanal, pentadecane (H. durvillaei), canthaxanthin, oleic acid, pentadecanoic acid, eicosane (C. lentillifera), pseudoephedrine, palmitic acid, monocaprin (C. racemosa), dictyohydroperoxide, squalene, fucosterol, saringosterol (D. dichotoma), and lutein, neophytadiene, cholest-4-en-3-one and cis-vaccenic acid (S. polycystum). Extensive studies on the seaweed isolates are highly recommended to understand their bioactivity and mechanisms of action, while highlighting their commercialization potential.


Introduction
Marine organisms have been widely used as sources of functional bioactive compounds over the years [1]. Among marine resources, seaweeds (multicellular marine algae) are well-documented natural sources of proteins, nitrogen compounds, carbohydrates as well as lipids, vitamins, minerals, pigments and volatile compounds [1,2]. Based on chlorophyll, seaweeds are divided into three groups-green algae (Chlorophyceae), red algae (Rhodophyceae), and brown algae (Phaeophyceae) [3]-and possess a wide range of biological potentials that are beneficial against several disorders such as cytotoxic, antioxidant, anti-inflammatory, and antimitotic activities [4,5]. Due to population growth, fast industrial growth, and the public's desire for natural products, worldwide demand for seaweed products is anticipated to grow even more in the years ahead [6].
Malaysia is part of the Coral Triangle, a geographical area in Southeast Asia and the Pacific that includes the oceans close to Indonesia, Malaysia, Philippines, Papua New Guinea, Timor-Leste and Solomon Islands. The temperatures of Malaysia's coastal waters make it ideal for the development and growth of a wide variety of seaweed species. The Table 1. Descriptions of North Bornean seaweed species.

Therapeutic Potential of North Bornean Seaweeds
Seaweeds are also known as sea vegetables and have been used for the treatment of various disorders [13][14][15][16]. Anti-inflammatory, antioxidant, antimicrobial, and anticancer properties as well as cardiovascular protection, renal protection, hepatoprotection, and neuroprotection are only a few of the medicinal activities of seaweed that have been previously described [9,[16][17][18][19][20][21][22]. Some of the protective actions of North Bornean seaweeds are discussed below.

Anti-Inflammatory Activity
Inflammation is a recognized defensive mechanism evolved in high-level organisms in response to stressors that disrupt bodily homeostasis. Microbial infections, tissue stress and some traumas are examples of hazards that cause inflammation with common symptoms of fever, redness, swelling and pain [23,24]. Overproduction of pro-inflammatory cytokines including tumor necrosis factor-alpha (TNF-α), interleukin (IL) (IL-6 and IL-1), prostaglandin E2 (PGE2), nitric oxide (NO), and enhanced production of reactive oxygen species (ROS) define the inflammatory response [25]. Increased activity of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) is associated with increased NO and PGE2 production [26].
K. alvarezii has been reported to have anti-inflammatory potential in asthma-induced rats. The extract changed circulating white blood cell levels, reduced mucin synthesis, and downregulated the expression of TNF-α, IL-4, nuclear factor kappa beta (NF-κB), epidermal growth factor receptor (EGFR) and matrix metalloproteinase . The consumption of seaweed may be useful for asthma patients. The extract decreases bronchiole smooth muscle thickness for airflow facilitation and decreases asthmatic inflammation, lung eosinophil infiltration, and mucin production [16].
The anti-inflammatory activity of C. lentillifera polysaccharides has been reported to have an inhibitory impact on lipopolysaccharide (LPS)-induced HT29 colorectal carcinoma cells, lowering the overproduction of TNF-α and IL-1β, SIgA and mucin2 (related proteins), as well as decreasing TNF-α and IL-1β expression [27]. C. racemosa polysaccharides have been reported to have anti-inflammatory potential and activate the hemoxigenase-1 (HO-1) pathway to sustain the production of hemoxigenase-1 enzyme, crucial for the prevention of inflammation [28].
In murine macrophage RAW 264.7 cells, the dichloromethane fraction of D. dichotoma extract at a concentration of 25 ug/mL inhibited the production of NO and PGE2, followed by a reduction in the expression of inducible nitric oxide synthase (iNOS) and COX-2 proteins, and iNOS and COX-2 mRNA in a dose-dependent pattern. COX-2 and iNOS are implicated in a variety of pathological processes, including inflammation. The solvent fractions of D. dichotoma extracts also decrease the mRNA expression of other cytokines including TNF-α, IL-1, and IL-6 in the murine macrophage cell line [29].
Anti-inflammatory and analgesic activity from brown algae S. polycystum has been reported using a mouse model with the paw edema method, where the mouse paw was inflamed and the hexane fraction of seaweed extract at a concentration of 70 mg/kg b.w. was applied. The anti-inflammatory effect was measured by the decreased percentage of edema size. The hexane fractions of S. polycystum extract significantly reduced the edema size compared to untreated mice [17].
Marine seaweeds from North Borneo are a good source of antioxidants [9,11,34,35]. In a study, the antioxidant potential of marine seaweeds from North Borneo was evaluated by the Trolox equivalent antioxidant capacity (TEAC) and ferric reducing antioxidant power (FRAP) methods and total phenolic content by the Folin-Ciocalteu method expressed as phloroglucinol equivalents (PGE) [9]. The antioxidation activities of the North Bornean seaweeds showed good radical-scavenging and reducing power potential. The radicalscavenging and reducing power activities of the seaweeds have been reported in K. alvarezii 1. 63 [9]. Among the above-mentioned seaweeds, C. lentillifera has high antioxidation activities followed by C. racemosa, S. polycystum, H. durvillaei, D. dichotoma, K. alvarezii and E. denticulatum; while in terms of TP, S. polycystum has indicated high values followed by C. lentillifera, C. racemosa, D. dichotoma, K. alvarezii, H. durvillaei and E. denticulatum [9].

Antimicrobial Activity
Pathogenic microbes including bacteria, fungi, viruses and parasites are responsible for the development of various diseases that arise in the community [36]. Seaweeds with various bioactive secondary metabolites act as antimicrobial agents [37,38].
The antibacterial potential of the aqueous extraction of K. alvarezii against Staphylococcus aureus (S. aureus) (Rosenbach, 1884) has been examined. Administration of the extract at a concentration of 200 mg/mL resulted in an inhibition zone of 10.03 mm [37]. The ethanol extract of K. alvarezii was also effective against S. aureus, Staphylococcus epidermidis  [18]. Regarding antiviral activity, it has been reported that red algal lectin ECA-2 obtained from K. alvarezii (currently known as KAA-2 of K. alvarezii) exhibited strong anti-influenza activity against a wide spectrum of influenza virus strains, including the newly evolving swine-origin H1N1-2009 influenza strain. The mechanism involved the direct binding of ECA-2 to the viral envelope protein hemagglutinin (HA) and inhibited influenza virus propagation [41].
The ethanol extract of E. denticulatum inhibited the growth of S. aureus with inhibition zones of 6.0-16.3 mm. Furthermore, the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values for E. denticulatum extract against S. aureus were 10% and 15%, respectively. At 10%, minimum bacterial growth was observed, the number of bacteria greatly decreased from 3.0 × 10 7 to 1.5 × 10 2 CFU/plate, and turbidity levels also decreased; while at 15% of the extract, no bacterial growth was noticed [42]. No antifungal activity of E. denticulatum extract has been reported against Aspergillus flavus (A. flavus) (Link) [43]. Sulphated polydigalactosides (carrageenans) extracted from E. denticulatum have been tested for in vitro antiviral activity against human herpes virus type 1 (HHV-1). Carrageenans indicated an antiviral impact by the inhibition of virus attachment and interference in a subsequent stage of the virus replicative cycle. HHV-1 viral DNA synthesis was reduced by 3 folds in cultures treated with sulphated polydigalactosides from E. denticulatum (0.75 mg/mL) [44].
The extracts of H. durvillaei has been reported to have antimicrobial effects. The presence of antimicrobial activities of H. durvillaei extract against pathogenic bacteria was determined using the disc diffusion method. The solvent extract of H. durvillaei inhibited the growth of P. aeruginosa (11.89 mm), S. aureus (12.22 mm), and Streptococcus pyogenes (S. pyogenes) Rosenbach, 1884 (10.67 mm), respectively. However, no fungicidal activity of the solvent extract of H. durvillaei has been reported against C. albicans [45].
The chloroform extracts of C. lentillifera were tested against Methicillin-resistant S. aureus (MRSA) and neuropathogenic Escherichia coli K1 (E. coli K1). Moderate antibacterial activity of 62.17% against MRSA and poor antibacterial impact against E. coli K1 of 12.42% were demonstrated by C. lentillifera extract at a concentration of 250 µg/mL [35]. However, no antibacterial effect from an aqueous extract of C. lentillifera , as compared with positive (enrofloxacin, 128 µg/mL) and negative controls [46]. The antiviral activity of C. lentillifera extract was tested against White Spot Syndrome Virus (WSSV) (family Nimaviridae, consisting of a large circular double-stranded DNA genome) [46,47]. WSSV infects shrimps and is characterized by the presence of circular white patches in the cuticle of the cephalothorax and abdominal segments, with a reddish to pinkish color. In Asia and Americas, WSSV caused mass mortalities (80-100%) of cultured shrimps [48]. The administration of C. lentillifera extract yielded very good outcomes. Shrimps injected with WSSV and C. lentillifera (1-10 mg/mL) preincubated solutions exhibited significantly lower mortality of 0.0-6.7%, compared with the positive control (100%) (only WSSV-injected). This inhibitory effect was further confirmed by the reduction in viral loads of WSSV, and C. lentillifera (1-10 mg/mL) expressed significantly lower viral loads (0.00-0.79 log 10 copies number/µg of total DNA, respectively) than the positive control (4.39 log 10 copies number/µg of total DNA) [46]. Fungicidal activities of C. lentillifera against L. thermophilum and H. sabahensis have been reported as well. An ethanol extract of C. lentillifera inhibited hyphal growths of L. thermophilum IPMB 1401, L. thermophilum IPMB 1601 and H. sabahensis IPMB 1603 [18].
A chloroform extract of C. racemosa demonstrated antibacterial activity against MRSA and E. coli K1. The extract of C. racemosa, at a concentration of 250 µg/mL, displayed a high antibacterial effect of 97.7% against MRSA, but a weak effect of 19.90% against E. coli K1. A methanol extract of C. racemosa (250 µg/mL) also showed antibacterial activity of 61.54% and 42.91% against MRSA and E. coli K1 [35], respectively. C. racemosa has been reported to show antifungal activity against A. flavus. An ethanol extract of the seaweed demonstrated the strongest inhibitory power with a 30 mm diameter inhibition zone against A. flavus [43]. The antiviral activity of a solvent extract of C. racemosa was demonstrated against the Chikungunya virus (CHIKV) [49]. The virus belongs to the alphavirus genus of the Togaviridae family, an RNA virus mostly spread by bites of Aedes aegypti and Aedes albopictus mosquitoes, which cause high fever, joint pain, back pain, vomiting, headache, kidney, liver, heart disease, etc. [50]. The antiviral potential of a solvent extract of C. racemosa was determined based on inhibition of the cytopathic effect caused by CHIKV on African monkey kidney epithelial (Vero) cells. Chloroform, ethyl acetate, ethanol, and methanol extracts (5 to 640 µg/mL) of C. racemosa showed a significant inhibition effect [49].
Methanol, dichloromethane and hexane extracts of D. dichotoma at a concentration of 1.5 mg/disc were investigated for in vitro antibacterial and antifungal activities. The results indicated that the methanol extract inhibited the growth of B. subtilis (6.5 mm) and S. aureus (7.5 mm). The dichloromethane extract inhibited the growth of B. subtilis (7.0 mm), Enterobacter aerogenes (E. aerogenes) (Hormaeche & Edwards, 1960) (6.5 mm), E. coli (6.5 mm), Proteus vulgaris (P. vulgaris) (11.0 mm) and Salmonella typhimurium (S. typhimurium) (Loeffler, 1892) (7.0 mm), whereas the hexane extract inhibited the growth of B. subtilis (9.0 mm) and S. aureus (7.5 mm) only [51]. The antibacterial activity of the ethanol extract of D. dichotoma has been shown against Salmonella typhi (S. typhi), Klebsiella pneumoniae (K. pneumoniae) (Schroeter, 1886) Trevisan, 1887 and Shigella boydii (S. boydii) (Ewing, 1949) [52]. The antifungal activity of diethyl ether, methanol, and acetone extracts of D. dichotoma has been reported against Mucor sp. and A. flavus [52], while no antifungal activity of the solvent extracts of D. dichotoma (1.5 mg/disc) has been observed against C. albicans [51]. The antiviral activity of various fractions of D. dichotoma extract has been tested against herpes simplex virus (HSV) and coxsackievirus B3 (CVB3) [53]. HSV belongs to the Herpesviridae Family, has a double-stranded DNA structure, infects humans, and causes a variety of illnesses ranging from mild mucocutaneous infections to life-threatening infections, whereas CVB3 belongs to the Picornaviridae Family, has a single-stranded RNA structure, and is responsible for a wide spectrum of human diseases, from asymptomatic to deadly infections [54,55]. The antiviral properties of the fractions were recorded in terms of virus plaque inhibition on a Vero cell monolayer. The fractions indicated moderated antiviral activities against both HSV and CVB3 viruses [53].
A solvent extract of S. polycystum was tested against human pathogenic bacteria. The methanol extract of the seaweed resulted in the inhibition of P. aeruginosa (15 mm), K. pneumoniae (16 mm), E. coli (19 mm), and S. aureus (20 mm) [56]. However, methanol and ethanol extracts of S. polycystum indicated no inhibition against B. subtilis or S. enteritidis. Similarly, no antifungal activity has been observed against A. niger [57].

Anticancer Activity
Cancer is one of the main causes of mortality in the world, and many research facilities are now focusing on the development of new anticancer medicines that could improve chemotherapy treatment and reduce mortality rates [58]. The protective role of marine products, and especially seaweeds found in North Borneo, in controlling chronic diseases such as cancer has been articulated [19,[59][60][61][62].
A solvent extract of K. alvarezii has been reported with anti-breast and anti-colorectal cancer potential. The anticancer activities were expressed with inhibitory concentration (IC 50 ) value (µg/mL). An IC 50 value of less than 100 is considered to indicate an active compound with anticancer properties. An ethanolic extract of K. alvarezii exhibited anticancer activity against human breast adenocarcinoma cell line MCF-7 with an IC 50 of 75.7 µg/mL, while ethyl acetate and hexane extracts showed anti-colorectal cancer activity against human colorectal carcinoma cell line HCT-116 with IC 50 values of 21.4 and 43.0 µg/mL, respectively [63].
The antitumor activity of E. denticulatum against Ehrlich carcinoma and Meth-A fibrosarcoma has been reported. Oral administration of the extract (1600 mg/kg b.w.) for 28 days resulted in the inhibition of Ehrlich carcinoma by 25% in tumor-implanted mice. Similarly, intraperitoneal administration of E. denticulatum extract (50 mg/kg b.w.) for 7 days resulted in the inhibition of Meth-A fibrosarcoma by 17% [19]. The anticancer activity of crude extracts of H. durvelaei was investigated against four cancer cell lines (A549, HT-29, PC-3, and AGS). The results indicated that administration of H. durvelaei extracts reduced the growth of AGS and HT-29 cell lines by 27.17% and 1.47%, respectively [61].
Oligosaccharides (β-1,3-xylooligosaccharides) obtained from C. lentillifera have been reported to show antitumor properties against human breast adenocarcinoma cell line MCF-7. Exposure to C. lentillifera oligosaccharides inhibited the growth of MCF-7 cells in a dose-dependent manner and induced apoptosis (triggered chromatin condensation and poly ADP-ribose polymerase degradation) [59].
Polysaccharide fractions (coded as CRP) obtained from C. racemosa have been reported to show antitumor activity in tumor-inoculated mice (H22 tumor). The results indicated that administration of C. racemosa polysaccharide fractions of different doses could significantly inhibit the H22 tumor. After 14 days of transplantation, the weight of tumors in mice without polysaccharide treatment increased to 1.02 g while the tumor weight in mice exposed to the polysaccharide at a dose of 100 mg/kg b.w./day by routine oral passage decreased to 0.47 g, and the tumor inhibition rate reached 53.9% [60].
The anticancer activity of sulphated polysaccharides (fucoidan) from S. polycystum at a concentration ranging from 25-150 µg/mL has been reported against human breast adenocarcinoma cell line MCF-7 via cell viability assay. Treatment with the sulphated polysaccharides indicated the highest percentage of inhibition (90.4%) against the MCF-7 cell line at 150 µg/mL with an estimated IC 50 of 50 µg/mL [64]. In another study, aside from MCF-7 cells, treatment with S. polycystum polysaccharide induced apoptosis in colorectal cancer cell lines (HCT-15 cell) [34].

Anti-Obesity and Cardiovascular Protection
The hypocholesterolemic effects of various marine algae and algal polysaccharides have been reported. The administration of extract significantly reduced serum total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C) and triglycerides (TG) [12,20].
E. denticulatum played a vital role in the reduction of fat absorption by the body via inhibition of pancreatic lipase [12]. Inhibiting the absorption of dietary fat is one of the most efficient methods to manage obesity and cardiovascular risks [65,66]. An E. denticulatum extract at a concentration of 3.8 mg/mL showed pancreatic lipase activity inhibition with an 83% reduction [12].
Treatment of HCF diet rats with C. lentillifera was reported to show anti-obesity and cardiovascular protection activity. Supplementation with 5% C. lentillifera extract for 16 weeks in HCF-diet rats reduced body weight by 39.5%, significantly increased HDL-C levels by 48.7%, reduced plasma TC by 18.4%, LDL-C by 34.6% and TG by 33.7%, and lowered plasma MDA level by 9%, GSH-Px by 31.8% and CAT by 3.14%, compared to the corresponding levels in high-cholesterol-diet rats [20].
The exposure of induced-hypercholesterolemia and -hypertriglyceridemia rats to S. polycystum significantly reduced body weight gain, plasma antioxidant enzymes and plasma lipid peroxidation to levels closer to those of healthy rats. Supplementation with 5% S. polycystum in rats fed a high-fat diet reduced body weight by 42.6%, significantly increased HDL-C levels by 16.2%, reduced plasma TC by 11.4%, LDL-C by 22% and TG by 7.69%, and decreased the plasma MDA level by 6.8%, GSH-Px by 43.4% and CAT by 15.7%, as compared to the corresponding levels in hypercholesterolemia and hypertriglyceridemia rats [20].

Hepatoprotection
Millions of people die each year as a result of hepatic diseases across the world [67,68]. The spread of hepatic disorders is aided by alcohol intake, obesity, nonalcoholic fatty liver disease, viral infection and medications [69][70][71][72][73]. Oxidative stress is one of the mechanisms underlying hepatotoxicity, which occurs when there is an imbalance between the production of reactive oxygen species (ROS) and the antioxidants' ability to scavenge them in the liver [74]. Overproduction of ROS results in the elevation of serum hepatic marker enzymes including serum glutamate pyruvate transaminase (SGPT) or alanine aminotransferase (ALT), serum glutamic-oxaloacetic transaminase (SGOT) or aspartate transaminase (AST), and alkaline phosphatase (ALP), an indication of liver damage. It also induces lipid peroxidation and alters levels of antioxidant enzymes including glutathione peroxidases (GPs), catalase (CAT), superoxide dismutase (SOD), glutathione S-transferase (GST), quinone reductase (QR), etc. [75][76][77].
The hepatoprotective activity of K. alvarezii ethanolic extract administered for 25 days against lead acetate-induced hepatic injury in mice has been investigated. The extract at a concentration of 800 mg/kg b.w. reduced AST, ALT and ALP levels by 15.79%, 18.52% and 16.11%, respectively, compared to lead acetate-treated mice (20 mg/kg b.w. orally once a day for 21 days). Mice administered with ethanol extract of K. alvarezii (800 mg/kg b.w.) also demonstrated a significant (p < 0.05) elevation in SOD and GPx levels by 45.94% and 18.78%, respectively, and a significant (p < 0.05) reduction in MDA level by 22.83%, compared with lead acetate-treated mice. Histological observations of mouse hepatic tissues treated with K. alvarezii ethanolic extract indicated improved hepatic cell structure, blood congestion, and fatty degeneration compared to lead acetate-treated mice [76].
A methanol extract of C. lentillifera demonstrated hepatoprotection against acetaminophen (n-acetyl-p-aminophenol; APAP) induced hepatic damage in juvenile zebrafish (aged 1-3 months). The administration of APAP to the control group at a concentration of 10 µM caused fish mortality; while the introduction of the methanol extract of C. lentillifera at concentrations of 10, 20 and 30 µg/l to tanks holding 10 µM APAP-treated groups reduced fish mortality. Histological observation by hematoxylin and eosin staining of zebrafish hepatic tissues exposed to 10 µM APAP and concurrently administered C. lentillifera extract indicated a reduction in hepatic necrosis, hepatocyte swelling, hepatocyte vacuolization and leukocyte infiltration in a dose-dependent manner, as compared to the control group treated solely with 10 µM APAP [78].
The protective effect of a solvent extract of S. polycystum was examined in acetaminophen (single dose administered intraperitoneally, 800 mg/kg b.w.) induced hepatic oxidative injured rats. The oral administration of S. polycystum extract in intoxicated rats at a concentration of 200 mg/kg b.w./day for 15 days reduced elevated levels of ALT (27.64%), AST (56.43%), LDH (43.38%), ALP (72.53%) and MDA (31.50%), compared to the levels in an APAP-administered control group [22].

Neuroprotection
Neuroprotection is a strategy for halting the progression of neurodegeneration [80]. Neurodegeneration is a multifaceted, complicated process that results in the death and loss of neuronal structures in the nervous system. Oxidative stress, calcium dysregulation, axonal transport deficiencies, mitochondrial dysfunction, inappropriate neuron-glial interactions, DNA damage and neuroinflammation are all underlying processes in neurodegeneration [80]. Seaweeds from North Borneo are rich in sulphated and non-sulphated polysaccharides and have been reported to have neuroprotection potential [21,81,82].
It was reported that an extract of K. alvarezii might be beneficial as a food supplement or medication for those who are prone to neurological disorders. In primary cultures of hippocampal neurons, the effects of K. alvarezii extracts on the development and complexity of neuronal cytoarchitecture were reported. A solvent extract of K. alvarezii with an optimal concentration of 1 µg/mL was added to primary cultures of fetal rat hippocampal neurons. The extract significantly elevated axonal length, number of secondary axonal collateral branches, length of primary dendrites and number of secondary dendritic branches by 58%, 8 folds, 68% and 2.6 folds, respectively, as compared to control [81].
Alzheimer's disease is a common neurologic disorder, responsible for brain shrinkage and cell death. It is the most prevalent type of dementia and one of the top four causes of mortality in developed countries [83]. So far, the primary symptomatic therapy for this condition has been based on the "cholinergic hypothesis," where the medications increase the level of acetylcholine in the brain by inhibiting the activity of the cholinesterase (acetylcholinesterase and butyrylcholinesterase) enzyme [84]. The anti-butyrylcholinesterase activity of a solvent extract of D. dichotoma has been reported. A methanol extract of D. dichotoma at a concentration of 1.3-6.5 mg/mL showed significant (p < 0.05) inhibition of cholinesterase enzyme (54.42%), compared to standard donepezil (cholinesterase inhibitor) (57.57%) at a concentration of 0.40-4.15 mg/mL [82].
The acetylcholinesterase and butyrylcholinesterase inhibitory activities of C. racemosa and S. polycystum at various concentrations (0.0125-0.2 mg/mL) have been determined. Solvent extracts of C. racemosa and S. polycystum indicated anti-acetylcholinesterase activities with IC 50 values ranging from 0.086-0.115 mg/mL, while C. racemosa extracts indicated anti-butyrylcholinesterase activity with an IC 50 value of 0.156 mg/mL [21].
A summary regarding the protective nature of the above-mentioned North Bornean seaweeds is shown in Table 2.

Methodology
The information was retrieved from multiple internet databases such as ScienceDirect, PubMed, Wiley, ACS publications, etc., and registers including theses and proceedings. Records were searched with keywords related to seaweed, North Borneo, distribution, taxonomy, bioactivity, secondary metabolites, and diseases. Around 250 records approximately from the year 2000 to 2021 were retrieved and screened. Among these, about 100 records were excluded due to being out of the scope of the review. Eventually, a total of 149 records were adopted for the current review paper, and data from organizations such as the World Health Organization were included as well.
Despite their excellent pharmacological characteristics, only K. alvarezii and E. denticulatum are widely cultivated, developed as a functional food source, and used for carrageenans production. Locally, C. lentillifera and C. racemosa are also consumed as a nutrition source. For future perspectives, studies on functional food development and cultivation techniques are highly recommended. Furthermore, extensive studies on the seaweed isolates are needed to understand their bioactivity and mechanisms of action, while highlighting their commercialization potential.

Conflicts of Interest:
The authors declare no conflict of interest.