Effects of Carrageenans on Biological Properties of Echinochrome

Sea urchin pigment echinochrome A (Ech), a water-insoluble compound, is the active substance in the cardioprotective and antioxidant drug Histochrome® (PIBOC FEB RAS, Moscow, Russia). It has been established that Ech dissolves in aqueous solutions of carrageenans (CRGs). Herein, we describe the effects of different types of CRGs on some properties of Ech. Our results showed that CRGs significantly decreased the spermotoxicity of Ech, against the sea urchin S. intermedius sperm. Ech, as well as its complex with CRG, did not affect the division and development of early embryos of the sea urchin. Ech reduced reactive oxygen species production (ROS) in neutrophils, caused by CRG. The obtained complexes of these substances with pro- and anti-activating ROS formation properties illustrate the possibility of modulating the ROS induction, using these compounds. The CRGs stimulate the induction of anti-inflammatory IL-10 synthesis, whereas Ech inhibits this synthesis and increases the production of the pro-inflammatory cytokines IL-6 and TNFα. The inclusion of Ech, in the complex with the CRGs, decreases Ech’s ability to induce the expression of pro-inflammatory cytokines, especially TNFα, and increases the induction of anti-inflammatory cytokine IL-10. Thus, CRGs modify the action of Ech, by decreasing its pro-inflammatory effect. Whereas, the Ech’s protective action towards human epithelial HT-29 cells remains to be unaltered in the complex, with κ/β-CRG, under stress conditions.


Introduction
With increasing awareness of functional properties of products from marine organisms, their attractiveness, both as a source of nutritious food items and stockpot of novel, biologically-active compounds, continuously expand [1]. The characteristic color of spines and armors of sea urchins are attributed to calcium salts of polyhydroxynaphthoquinone pigments derivatives-spinochromes and echinochromes-exhibiting a vast range of pharmacological activities. One of the most popular pigments is the echinochrome A (6-ethyl-2,3,5,7,8-pentahydroxy-1,4-naphthoquinone), which is known to be a biologically-active compound with antimicrobial, antialgal, and antioxidant activities [2]. Most of all, it has been ascertained that a treatment with echinochrome protected the mitochondrial functions in cardiomyocytes, against the acardiotoxic drugs (tert-Butyl hydroperoxide, sodium nitroprusside) [3]. There are controversial data in the literature, in terms of Ech's capacity to activate an immune response, some data suggest that Ech has an ability to activate inflammation, whereas others suggest that it can suppress inflammation [4,5]. Pharmacological studies in vitro and in vivo or absence (λ) of 3,6-anhydrogalactose units (DA). The degree of sulfation decreased in the following row: λ > ι/κ > κ > κ/β.   [20] C. armatus λ G2S D2S, 6S 26 [20] C. armatus κ G4S DA 22 [21] T.crinitus κ/β G4S/G DA/DA 19 [22] A. flabelliformis ι/κ G4S/G4S DA2S/DA 20

Toxicity
As a cellular model to study spermotoxic and embryotoxic properties, we used the spermatozoa and developing embryos of the sea urchin S. intermedius.
The spermotoxicities of Ech, CRGs, and the complexes Ech/CRGs were investigated by the Sea Urchins Sperm Cell Toxicity Test (SUSCT)-test [23,24]. These activities were determined by the degree of inhibition of the spermatozoa's ability to fertilize the sea urchin eggs. Previously, all types of CRGs (κ, λ, ι/κ) were investigated for spermotoxicity in seawater, at a concentration 50 to 200 μg mL −1 . The results showed that all of the studied CRGs had no toxic effect on the spermatozoa fertilization ability, at these concentrations. The current study with Ech in the concentration range from 1 to 10 μg mL −1 revealed that this substance exhibited spermotoxicity. The spermotoxicity of Ech was expressed in the 50% inhibition of the spermatozoa's ability to fertilize the egg-cells (IC50 values were of 3 μg mL −1 ), at a sperm:egg ratio of 300:1. When the Eсh was added to a solution of CRGs, with a concentration of the 100 μg mL −1 , the spermotoxicity of the Ech decreased significantly. The higher the concentration of the Ech, the greater was the protective effect of the CRG (Figure 1a). The protection of various CRGs types, against the spermotoxicity of the Ech (C = 3 μg mL −1 ) was studied by the SUSCT-test, at the spermatozoa to eggs ratios of 300:1 and 150:1 (Figure 1b). From the data presented in Figure 1b, it can be seen that λ-CRG, with a higher degree of sulfation, showed a greater protective activity. This dependence of the protective effects of the CRGs on their structures, was particularly noticeable at the spermatozoa to eggs ratio of 150:1, when the sensitivity of the method was the highest.
To determine the embryotoxic effects of the Ech and its complex, with the CRG (100 μg mL −1 ), fertilized eggs from the sea urchins were used. In a concentration range from 2-36 μg mL −1 , the Ech did not affect the division and development of early embryos of the sea urchin Strongylocentrotus intermedius, as well as its complex with the CRGs.

Toxicity
As a cellular model to study spermotoxic and embryotoxic properties, we used the spermatozoa and developing embryos of the sea urchin S. intermedius.
The spermotoxicities of Ech, CRGs, and the complexes Ech/CRGs were investigated by the Sea Urchins Sperm Cell Toxicity Test (SUSCT)-test [23,24]. These activities were determined by the degree of inhibition of the spermatozoa's ability to fertilize the sea urchin eggs. Previously, all types of CRGs (κ, λ, ι/κ) were investigated for spermotoxicity in seawater, at a concentration 50 to 200 µg mL −1 . The results showed that all of the studied CRGs had no toxic effect on the spermatozoa fertilization ability, at these concentrations. The current study with Ech in the concentration range from 1 to 10 µg mL −1 revealed that this substance exhibited spermotoxicity. The spermotoxicity of Ech was expressed in the 50% inhibition of the spermatozoa's ability to fertilize the egg-cells (IC 50 values were of 3 µg mL −1 ), at a sperm:egg ratio of 300:1. When the Ech was added to a solution of CRGs, with a concentration of the 100 µg mL −1 , the spermotoxicity of the Ech decreased significantly. The higher the concentration of the Ech, the greater was the protective effect of the CRG (Figure 1a). The protection of various CRGs types, against the spermotoxicity of the Ech (C = 3 µg mL −1 ) was studied by the SUSCT-test, at the spermatozoa to eggs ratios of 300:1 and 150:1 (Figure 1b). From the data presented in Figure 1b, it can be seen that λ-CRG, with a higher degree of sulfation, showed a greater protective activity. This dependence of the protective effects of the CRGs on their structures, was particularly noticeable at the spermatozoa to eggs ratio of 150:1, when the sensitivity of the method was the highest.
To determine the embryotoxic effects of the Ech and its complex, with the CRG (100 µg mL −1 ), fertilized eggs from the sea urchins were used. In a concentration range from 2-36 µg mL −1 , the Ech did not affect the division and development of early embryos of the sea urchin Strongylocentrotus intermedius, as well as its complex with the CRGs. The spermatozoa fertilizing ability of various types of CRGs (100 μg mL −1 ), in the presence of Ech (3 mg mL −1 ). * p < 0.05.

Reactive Oxygen Species (ROS)-Inducing Activity of the CRG and the Ech on the Human Blood Cells
The ROS induction in human neutrophils, in the presence of the Ech and its complexes with CRGs, was determined with the Ech concentration varying from 1 to 10 μg mL −1 . To assess the effect of the content of the polysaccharide in the complex with the Ech, on the formation of ROS, we used CRG concentrations in the range of 5 to 200 μg mL −1 . Thus, complexes with different CRGs/Ech ratios (5:1, 10:1, and 20:1) were prepared.
The corresponding effects were detected using a fluorescent probe and measured by means of flow cytometry ( Figure 2). Lipopolysaccharide (LPS) from E. coli was used as a reference immunomodulator, in the current test, and the ROS production induced by the LPS, as a positive control, was approximately twice as much as the negative control (the vehicle). At low concentrations, the activity of Ech towards the ROS formation was comparable to the negative control, whereas at high concentrations its effect was lower than that of the control by 20%. The influence of the CRGs on the activation of ROS, at lower concentrations, was not significant except for the λ-CRG. In contrast, the CRGs at a concentration of 100 μg mL −1 intensified the induction of the ROS by up to 25-55%, relative to the negative control. The addition of the Ech to the CRGs, especially at high concentrations, resulted in significant diminishment of the ROS formation induced by the CRGs alone. The action of the complexes was compared to the negative control, where at higher concentrations, the effect of the samples was more noticeable.

Reactive Oxygen Species (ROS)-Inducing Activity of the CRG and the Ech on the Human Blood Cells
The ROS induction in human neutrophils, in the presence of the Ech and its complexes with CRGs, was determined with the Ech concentration varying from 1 to 10 µg mL −1 . To assess the effect of the content of the polysaccharide in the complex with the Ech, on the formation of ROS, we used CRG concentrations in the range of 5 to 200 µg mL −1 . Thus, complexes with different CRGs/Ech ratios (5:1, 10:1, and 20:1) were prepared.
The corresponding effects were detected using a fluorescent probe and measured by means of flow cytometry ( Figure 2). Lipopolysaccharide (LPS) from E. coli was used as a reference immunomodulator, in the current test, and the ROS production induced by the LPS, as a positive control, was approximately twice as much as the negative control (the vehicle). At low concentrations, the activity of Ech towards the ROS formation was comparable to the negative control, whereas at high concentrations its effect was lower than that of the control by 20%. The influence of the CRGs on the activation of ROS, at lower concentrations, was not significant except for the λ-CRG. In contrast, the CRGs at a concentration of 100 µg mL −1 intensified the induction of the ROS by up to 25-55%, relative to the negative control. The addition of the Ech to the CRGs, especially at high concentrations, resulted in significant diminishment of the ROS formation induced by the CRGs alone. The action of the complexes was compared to the negative control, where at higher concentrations, the effect of the samples was more noticeable.

IL-10-Inducing Action of the CRGs and the Ech on the Human Blood Cells
The action of the carragenans, Ech, and their complexes on the pro-inflammatory (IL-6 and TNFα) and anti-inflammatory (IL-10) cytokines induction was conducted. In this experiment, Eсh was used at one concentration, 1 μg mL −1 whereas, CRG concentrations individually and in complexes, varied in the following row 5.0, 10.0, and 20 μg mL −1 . As seen in Figure 3, κ-and λ-types (10 and 20 μg mL −1 ) induced the expression of IL-10 in cells, by approximately 120 and 100 pg mL −1 , in comparison to the negative control, respectively. Ech significantly inhibited the synthesis of IL-10, reducing the induction of this anti-inflammatory cytokine by 50%, compared to the control. At the same time, the inclusion of Ech into the CRG complex increased the induction of IL-10 synthesis, compared to Ech. The greatest effect was shown by the complex of Ech with ι/κ-CRG ( Figure 3). Regarding the pro-inflammatory cytokines, Ech (1 μg mL −1 ) was a strong inductor, in comparison to the highest concentrations of the CRGs, but its action was decreased, especially in the complexes with the κ-or λ-types, by about 300 pg mL −1 for IL-6 and 350 pg mL −1 for TNFα. However, the combined action of the CRNs and the Ech complexes on the IL-6 still remained high, compared to the control. The ι/κ-CRG influenced the effect of Ech with less degree than the others, as complexes had formed. Thus, the CRGs modified the activity of Ech by decreasing its pro-inflammatory effect.

IL-10-Inducing Action of the CRGs and the Ech on the Human Blood Cells
The action of the carragenans, Ech, and their complexes on the pro-inflammatory (IL-6 and TNFα) and anti-inflammatory (IL-10) cytokines induction was conducted. In this experiment, Eсh was used at one concentration, 1 μg mL −1 whereas, CRG concentrations individually and in complexes, varied in the following row 5.0, 10.0, and 20 μg mL −1 . As seen in Figure 3, κ-and λ-types (10 and 20 μg mL −1 ) induced the expression of IL-10 in cells, by approximately 120 and 100 pg mL −1 , in comparison to the negative control, respectively. Ech significantly inhibited the synthesis of IL-10, reducing the induction of this anti-inflammatory cytokine by 50%, compared to the control. At the same time, the inclusion of Ech into the CRG complex increased the induction of IL-10 synthesis, compared to Ech. The greatest effect was shown by the complex of Ech with ι/κ-CRG ( Figure 3). Regarding the pro-inflammatory cytokines, Ech (1 μg mL −1 ) was a strong inductor, in comparison to the highest concentrations of the CRGs, but its action was decreased, especially in the complexes with the κ-or λ-types, by about 300 pg mL −1 for IL-6 and 350 pg mL −1 for TNFα. However, the combined action of the CRNs and the Ech complexes on the IL-6 still remained high, compared to the control. The ι/κ-CRG influenced the effect of Ech with less degree than the others, as complexes had formed. Thus, the CRGs modified the activity of Ech by decreasing its pro-inflammatory effect.

IL-10-Inducing Action of the CRGs and the Ech on the Human Blood Cells
The action of the carragenans, Ech, and their complexes on the pro-inflammatory (IL-6 and TNFα) and anti-inflammatory (IL-10) cytokines induction was conducted. In this experiment, Eсh was used at one concentration, 1 μg mL −1 whereas, CRG concentrations individually and in complexes, varied in the following row 5.0, 10.0, and 20 μg mL −1 . As seen in Figure 3, κ-and λ-types (10 and 20 μg mL −1 ) induced the expression of IL-10 in cells, by approximately 120 and 100 pg mL −1 , in comparison to the negative control, respectively. Ech significantly inhibited the synthesis of IL-10, reducing the induction of this anti-inflammatory cytokine by 50%, compared to the control. At the same time, the inclusion of Ech into the CRG complex increased the induction of IL-10 synthesis, compared to Ech. The greatest effect was shown by the complex of Ech with ι/κ-CRG (Figure 3). Regarding the pro-inflammatory cytokines, Ech (1 μg mL −1 ) was a strong inductor, in comparison to the highest concentrations of the CRGs, but its action was decreased, especially in the complexes with the κ-or λ-types, by about 300 pg mL −1 for IL-6 and 350 pg mL −1 for TNFα. However, the combined action of the CRNs and the Ech complexes on the IL-6 still remained high, compared to the control. The ι/κ-CRG influenced the effect of Ech with less degree than the others, as complexes had formed. Thus, the CRGs modified the activity of Ech by decreasing its pro-inflammatory effect.

IL-10-Inducing Action of the CRGs and the Ech on the Human Blood Cells
The action of the carragenans, Ech, and their complexes on the pro-inflammatory (IL-6 and TNFα) and anti-inflammatory (IL-10) cytokines induction was conducted. In this experiment, Eсh was used at one concentration, 1 μg mL −1 whereas, CRG concentrations individually and in complexes, varied in the following row 5.0, 10.0, and 20 μg mL −1 . As seen in Figure 3, κ-and λ-types (10 and 20 μg mL −1 ) induced the expression of IL-10 in cells, by approximately 120 and 100 pg mL −1 , in comparison to the negative control, respectively. Ech significantly inhibited the synthesis of IL-10, reducing the induction of this anti-inflammatory cytokine by 50%, compared to the control. At the same time, the inclusion of Ech into the CRG complex increased the induction of IL-10 synthesis, compared to Ech. The greatest effect was shown by the complex of Ech with ι/κ-CRG (Figure 3). Regarding the pro-inflammatory cytokines, Ech (1 μg mL −1 ) was a strong inductor, in comparison to the highest concentrations of the CRGs, but its action was decreased, especially in the complexes with the κ-or λ-types, by about 300 pg mL −1 for IL-6 and 350 pg mL −1 for TNFα. However, the combined action of the CRNs and the Ech complexes on the IL-6 still remained high, compared to the control. The ι/κ-CRG influenced the effect of Ech with less degree than the others, as complexes had formed. Thus, the CRGs modified the activity of Ech by decreasing its pro-inflammatory effect.

IL-10-Inducing Action of the CRGs and the Ech on the Human Blood Cells
The action of the carragenans, Ech, and their complexes on the pro-inflammatory (IL-6 and TNFα) and anti-inflammatory (IL-10) cytokines induction was conducted. In this experiment, Ech was used at one concentration, 1 µg mL −1 whereas, CRG concentrations individually and in complexes, varied in the following row 5.0, 10.0, and 20 µg mL −1 . As seen in Figure 3, κand λ-types (10 and 20 µg mL −1 ) induced the expression of IL-10 in cells, by approximately 120 and 100 pg mL −1 , in comparison to the negative control, respectively. Ech significantly inhibited the synthesis of IL-10, reducing the induction of this anti-inflammatory cytokine by 50%, compared to the control. At the same time, the inclusion of Ech into the CRG complex increased the induction of IL-10 synthesis, compared to Ech. The greatest effect was shown by the complex of Ech with ι/κ-CRG (Figure 3). Regarding the pro-inflammatory cytokines, Ech (1 µg mL −1 ) was a strong inductor, in comparison to the highest concentrations of the CRGs, but its action was decreased, especially in the complexes with the κor λ-types, by about 300 pg mL −1 for IL-6 and 350 pg mL −1 for TNFα. However, the combined action of the CRNs and the Ech complexes on the IL-6 still remained high, compared to the control. The ι/κ-CRG influenced the effect of Ech with less degree than the others, as complexes had formed. Thus, the CRGs modified the activity of Ech by decreasing its pro-inflammatory effect.

Influence of the CRGs, the Ech and Their Complex, on the HT-29 Tumor Cells
The effect of the Ech, alone and in carrageenans complexes, on the HT-29 cells treated with ethanol was investigated. The exposure of cells to EtOH permits an assessment of the samples' ability to affect cell viability and, as a result, the permeability of the epithelial monolayer. All of the investigated samples were inert, in response to the intestinal epithelial HT-29 cells, under normal conditions. Under stress conditions, only the κ/β-CRG and the Ech, as well their complex, restored the cell viability after exposure to the EtOH. As to the CRG, the most prominent action was detected for the lowest concentrations, where protective effect preserved. The complex of κ/β-CRG with the Ech, also possessed an ability to restore the HT-29 cells after an exposure to ethanol (Figure 4).

Influence of the CRGs, the Ech and Their Complex, on the HT-29 Tumor Cells
The effect of the Ech, alone and in carrageenans complexes, on the HT-29 cells treated with ethanol was investigated. The exposure of cells to EtOH permits an assessment of the samples' ability to affect cell viability and, as a result, the permeability of the epithelial monolayer. All of the investigated samples were inert, in response to the intestinal epithelial HT-29 cells, under normal conditions. Under stress conditions, only the κ/β-CRG and the Ech, as well their complex, restored the cell viability after exposure to the EtOH. As to the CRG, the most prominent action was detected for the lowest concentrations, where protective effect preserved. The complex of κ/β-CRG with the Ech, also possessed an ability to restore the HT-29 cells after an exposure to ethanol (Figure 4).

IL-10-Inducing Action of the CRGs and the Ech on the Human Blood Cells
The action of the carragenans, Ech, and their complexes on the pro-inflam TNFα) and anti-inflammatory (IL-10) cytokines induction was conducted. In thi was used at one concentration, 1 μg mL −1 whereas, CRG concentrations ind complexes, varied in the following row 5.0, 10.0, and 20 μg mL −1 . As seen in Figur (10 and 20 μg mL −1 ) induced the expression of IL-10 in cells, by approximately 120 in comparison to the negative control, respectively. Ech significantly inhibited the reducing the induction of this anti-inflammatory cytokine by 50%, compared to t same time, the inclusion of Ech into the CRG complex increased the induction o compared to Ech. The greatest effect was shown by the complex of Ech with ι/ Regarding the pro-inflammatory cytokines, Ech (1 μg mL −1 ) was a strong inductor the highest concentrations of the CRGs, but its action was decreased, especially in t

tion of the CRGs and the Ech on the Human Blood Cells
e carragenans, Ech, and their complexes on the pro-inflammatory (IL-6 and mmatory (IL-10) cytokines induction was conducted. In this experiment, Eсh ncentration, 1 μg mL −1 whereas, CRG concentrations individually and in the following row 5.0, 10.0, and 20 μg mL −1 . As seen in Figure 3, κ-and λ-types duced the expression of IL-10 in cells, by approximately 120 and 100 pg mL −1 , egative control, respectively. Ech significantly inhibited the synthesis of IL-10, n of this anti-inflammatory cytokine by 50%, compared to the control. At the ion of Ech into the CRG complex increased the induction of IL-10 synthesis, e greatest effect was shown by the complex of Ech with ι/κ-CRG (Figure 3). lammatory cytokines, Ech (1 μg mL −1 ) was a strong inductor, in comparison to

L-10-Inducing Action of the CRGs and the Ech on the Human Blood Cells
The action of the carragenans, Ech, and their complexes on the pro-inflammatory (IL-6 and α) and anti-inflammatory (IL-10) cytokines induction was conducted. In this experiment, Eсh used at one concentration, 1 μg mL −1 whereas, CRG concentrations individually and in plexes, varied in the following row 5.0, 10.0, and 20 μg mL −1 . As seen in Figure 3, κ-and λ-types nd 20 μg mL −1 ) induced the expression of IL-10 in cells, by approximately 120 and 100 pg mL −1 , mparison to the negative control, respectively. Ech significantly inhibited the synthesis of IL-10, cing the induction of this anti-inflammatory cytokine by 50%, compared to the control. At the e time, the inclusion of Ech into the CRG complex increased the induction of IL-10 synthesis, pared to Ech. The greatest effect was shown by the complex of Ech with ι/κ-CRG (Figure 3). rding the pro-inflammatory cytokines, Ech (1 μg mL −1 ) was a strong inductor, in comparison to = 20 µg mL −1 , final value. * p < 0.05.

Influence of the CRGs, the Ech and Their Complex, on the HT-29 Tumor Cells
The effect of the Ech, alone and in carrageenans complexes, on the HT-29 cells treated with ethanol was investigated. The exposure of cells to EtOH permits an assessment of the samples' ability to affect cell viability and, as a result, the permeability of the epithelial monolayer. All of the investigated samples were inert, in response to the intestinal epithelial HT-29 cells, under normal conditions. Under stress conditions, only the κ/β-CRG and the Ech, as well their complex, restored the cell viability after exposure to the EtOH. As to the CRG, the most prominent action was detected for the lowest concentrations, where protective effect preserved. The complex of κ/β-CRG with the Ech, also possessed an ability to restore the HT-29 cells after an exposure to ethanol (Figure 4).

Discussion
Ech, a water-insoluble compound, is the active substance (P N002362/01) of the drug Histochrome ® , registered in the Russian Federation. Earlier we have shown that Ech is soluble in aqueous solutions of CRGs, up to the concentration of 0.1 mg mL −1 . Moreover, the CRG environment protects the Ech from autooxidation [11]. In this work, we showed that carrageenans modified the biological activity of the Ech.
One of the manifestations of the biological effect of the drug is its ability to cause some disorders in the development and death of embryos (spermotoxic, embryotoxic, and cytostatic activities). The widespread use of the sea urchin embryos to test the toxicological and pharmacological effects of various drugs is due to the simplicity of the incubation of the synchronously developing embryos, under controlled conditions, and the ease of the intravital observation. The influence of the Ech and its complex with CRG, on sperm, was determined by the degree to which it inhibited the ability of spermatozoa to fertilize the sea urchin eggs and the further development of the early embryos of sea urchins, in comparison to the control. As the results showed, the CRGs significantly decreased the spermotoxicity of the Ech, towards the sea urchin S. intermedius sperm. Furthermore, neither the Ech, nor its complex with CRG, affected the division and development of the early embryos of the sea urchin.
Oxidative processes occurring during the neutrophils activation could be traced by the change in the ROS production [25]. In the case of the phagocytosis of the pathogens, the ROS were produced by the nicotinamide adenine dinucleotide phosphate oxidase (NOX) in a small volume of the phagosome [26]. During our study, we used an APF fluorescent probe (2-[6-(4-amino)phenoxy-3Hxanthen-3-on-9]benzoic acid), with a strong specificity towards the species of the reactive oxygen, localized predominantly in the phagosomes [27]. It should be noted that, in general, the activating effect of the CRGs was dependent on the polysaccharide concentration and the sulfation degree. In this study, a positive correlation between the impact on the ROS formation and the sulfation degree of the CRG (except for its highest concentration) was observed. Generally, the complex of the λ-CRG, with the Ech, was the most active out of all three types, their effect (complexes of the CRGs and the Ech with concentrations of 200:5 and 100:5 μg mL −1 ) was about 15%, compared to control (Figure 2). The importance of the CRG sulfation degree, with regards to monocyte behaviour, have also been observed, previously [28].

Discussion
Ech, a water-insoluble compound, is the active substance (P N002362/01) of the drug Histochrome ® , registered in the Russian Federation. Earlier we have shown that Ech is soluble in aqueous solutions of CRGs, up to the concentration of 0.1 mg mL −1 . Moreover, the CRG environment protects the Ech from autooxidation [11]. In this work, we showed that carrageenans modified the biological activity of the Ech.
One of the manifestations of the biological effect of the drug is its ability to cause some disorders in the development and death of embryos (spermotoxic, embryotoxic, and cytostatic activities). The widespread use of the sea urchin embryos to test the toxicological and pharmacological effects of various drugs is due to the simplicity of the incubation of the synchronously developing embryos, under controlled conditions, and the ease of the intravital observation. The influence of the Ech and its complex with CRG, on sperm, was determined by the degree to which it inhibited the ability of spermatozoa to fertilize the sea urchin eggs and the further development of the early embryos of sea urchins, in comparison to the control. As the results showed, the CRGs significantly decreased the spermotoxicity of the Ech, towards the sea urchin S. intermedius sperm. Furthermore, neither the Ech, nor its complex with CRG, affected the division and development of the early embryos of the sea urchin.
Oxidative processes occurring during the neutrophils activation could be traced by the change in the ROS production [25]. In the case of the phagocytosis of the pathogens, the ROS were produced by the nicotinamide adenine dinucleotide phosphate oxidase (NOX) in a small volume of the phagosome [26]. During our study, we used an APF fluorescent probe (2-[6-(4-amino)phenoxy-3H-xanthen-3-on-9]benzoic acid), with a strong specificity towards the species of the reactive oxygen, localized predominantly in the phagosomes [27]. It should be noted that, in general, the activating effect of the CRGs was dependent on the polysaccharide concentration and the sulfation degree. In this study, a positive correlation between the impact on the ROS formation and the sulfation degree of the CRG (except for its highest concentration) was observed. Generally, the complex of the λ-CRG, with the Ech, was the most active out of all three types, their effect (complexes of the CRGs and the Ech with concentrations of 200:5 and 100:5 µg mL −1 ) was about 15%, compared to control (Figure 2). The importance of the CRG sulfation degree, with regards to monocyte behaviour, have also been observed, previously [28].
In the complexes of the Ech with polysaccharides, containing 3,6-anhydrogalactose and the lower sulfate group contents (κ, ι/κ), the resultant action was closer to the level of the Ech alone. This was supported by results from the literature, which reported that the Ech significantly prevented an increase in the ROS levels in rat cardiac myoblast H9c2 cells and cardiomyocytes induced by some cardiotoxic agents [3], as well as in intraocular inflammation caused by endotoxin-induced uveitis [29]. Overall, this experiment indicated the modulation of the inductions of the ROS, in complexes with substances containing pro-(CRGs) and anti-(Ech) activating properties.
Depending on the ROS location in cells, the function of these molecules changes enormously. For example, mitochondrial ROS have a particularly interesting role in the immune response, since these ROS are currently considered essential for pathways initiating the production of pro-inflammatory cytokines [30]. The influence of the investigated samples on the synthesis of the immune mediators enabled the study of another facet of their immune activity, both separately and as complexes. Pro-inflammatory cytokines were exemplified by the IL-6, the most important inducer of the acute-phase proteins, and the TNFα, another pro-inflammatory molecule with cytotoxic effects in antitumor immunity, whereas the IL-10 is an important immunoregulatory cytokine with multiple biologic effects and strong tendencies of anti-inflammatory action [31]. The CRGs stimulated the induction of anti-inflammatory IL-10, whereas, the Ech inhibited the synthesis of this cytokine, and the addition of the CRGs to the Ech increased the induction of the expression of the anti-inflammatory IL-10 ( Figure 3). Ech, at a concentration 1 µg mL −1 , increased the IL-6 and TNFα synthesis; however, the complexes with CRGs exhibited much less activity in the case of synthesizing the pro-inflammatory cytokine TNFα. The effect of the Ech on the cytokine balance towards the pro-inflammatory response corresponded to the literature data, which reported that spinochromes act as inductors of TNF-α production in LPS-stimulated macrophage cell cultures [5]. Another study underlined a pro-inflammatory action of the naphthoquinones, in mice [32].
Literature data suggest that the CRGs do not affect the epithelial cells of human gastrointestinal tract [33], but the influence of the Ech towards these cells, which is of special interest when one considers an oral administration of a drug, has not been investigated, to our knowledge.
HT-29 is a colorectal cancer cell line used as an in vitro model, for the intestinal epithelium, because it is a mucin secreting cell line which retains many features attributed to the lower small intestine [34]. Previously we have studied the influence of CRGs on these cells, under stress conditions and have found out that only the low-sulfated CRG had a protective action towards the HT-29 intestinal epithelial cells [35]. Our purpose in the study described in this report, was to determine the protective action of the Ech alone and in combination with the low-sulfated CRG on the survival of monolayers of these cells, treated with EtOH ( Figure 4). The stress effect of ethanol on the state of the HT-29 cells provided an opportunity to assay the protective properties of polysaccharides from the red algae and the Ech. The Ech (1 µg mL −1 ) also preserved the HT-29 cells, under stress conditions, to an extent similar to the κ/β-CRG (25 µg mL −1 ). These results provide an opportunity to propose the CRGs as a possible matrix system, for oral delivery of Ech, which preserves the Ech-favorable qualities and mitigates its negative biological properties.
In general, the CRGs modified the Ech toxicity and the immunological properties. Our results showed that the CRGs significantly decreased the spermotoxicity of the Ech, against the sea urchin S. intermedius sperm. The Ech, as well as its complex with CRG, did not affect the division and development of the early embryos of the sea urchin. The influence of the investigated substances on the induction of the ROS, in the neutrophils, confirmed that Ech in a complex with a polysaccharide inhibited the induction of ROS induced by CRG.
The complexes obtained by us illustrated the modulation of the ROS induction, by these substances, with pro-(CRGs) and anti-(Ech) activating properties of the initial components. The CRG decreased the Ech's ability to induce the expression of pro-inflammatory cytokines and increased the expression of anti-inflammatory cytokines. Whereas, the Ech's protective action towards the intestinal cells exposed to EtOH, remained invariable in the complex with the κ/β-CRG.

Materials and Methods
The standardized echinochrome (pentahydroxyethylnaphthoquinone, Ech), registration number in the Russian Federation was P N002362/01 [Russian State Register of Drugs (as of 5 December 2016) Part 2]. It was obtained in powder form, from the G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Vladivostok. The purity of the Ech (99.0%) was confirmed by liquid chromatography, coupled with mass spectrometry (LC-MS) data (Shimadzu LCMS-2020, Kyoto, Japan). The purified Ech that looked like red-brown needles, was soluble in ethanol, had a melting point of 219-221.5 • C, and a similar nuclear magnetic resonance (NMR) spectra to that reported previously in Reference [36]. We used an ethanolic solution of the Ech, at a concentration 10 mg mL −1 , as a stock solution.
The CRGs were isolated by aqueous extraction from the Chondrus armatus (Gigartinaceae), Tichocarpus crinitus (Tichocarpaceae), and Anfeltiopsis flabelliformis (Phyllophoraceae) red algae, harvested along the Russian coast of the Japanese Sea. The polysaccharides were separated into gelling KCl-insoluble and non-gelling KC1-soluble fractions and their structures were established according to the published protocols [20][21][22]. Viscosimetric molecular weights of the CRGs were calculated using

Sea Urchin Models
The test samples in these experiments were polysaccharides of three CRG types. They were dissolved in sea water at 50 • C, to the level of the initial concentrations, from 0.5 to 1.0 mg mL −1 . Ech dissolved in 50% EtOH was used at the initial concentrations of 0.5 and 1 mg mL −1 . Adult sea urchins Strongylocentrotus intermedius (collected in the Troitsa Bay (Peter the Great Bay, the Sea of Japan) during August-September 2017, at a depth of 5-10 m) were stored in an aquarium with a closed-filter system, at a seawater temperature of 20 • C and salinity of 32 ± 0.5‰. Pooling male and female gametes and eggs, fertilizations were performed according to the standard procedures described in References [37,38]. The quality of the isolated sperms and eggs was checked with fertilization, prior to experiment. The fertilization membrane was formed within 1-2 min, after insemination, in at least 95-99% of the eggs, under normal conditions.

Sea Urchins Sperm Cell Toxicity Test (SUSCT Test)
We used the standard bioassay record of the SUSCT test for the analysis of the obtained preparations [23,24]. Sperm from sea urchins (15 × 10 6 cell mL −1 ), prior to the experiment, were sustained in seawater for 30 min, with various concentrations of the substances. Next, the spermatozoa were added to the suspension of eggs (2.5 × 10 3 cell mL −1 ). The final sperm:egg ratios were about 300 and 150:1. After 15 min, the percentage of fertilized eggs were counted on a Motic AE 21 inverted microscope (Xiamen, China). The experiments were carried out in triplicate using a 12-well plate. The effect of substance toxicity was assessed, visually, according to the number of unfertilized eggs in the four fields of view, in each experiment. The number of eggs fertilized by the sperms, after incubation in the seawater, without substances (control), was assumed to be 95-100%.

Sea Urchin Embryos Development Test
The preliminary fertilized eggs (2.5 × 10 3 cell mL −1 ) were stored in seawater, with different concentrations of the tested Ech (10 to 40 µg mL −1 ) and its complexes with CRGs, for 30 min, after which a suspension of native sperm was added. The number of embryos developed up to the stage of 2-4 blastomeres and of early blastula, in the presence of the test compounds, was evaluated using a microscope.

Ethical Approval for Human Blood Samples
The medical ethical committee of the local hospital (Vladivostok, Russian Federation) approved the study protocol. All subjects who participated in the experiments wrote an informed consent.

Leukocytes
Leukocytes were rapidly isolated from venous citrated blood by lyzing erythrocytes in a solution containing 0.15 M NH 4 Cl, 10 mM NaHCO 3 , and 0.1 mM EDTA [39].

Detection of Reactive Oxygen Production
Reactive oxygen production was detected by flow cytometry, with APF, as described elsewhere [40]. Cells (200,000 cells/well) were incubated for 1 hour, with the samples (12.5, 25, 50, and 100 µg mL −1 ; final value). Free cells with (phosphate buffer saline) PBS, instead of the samples, were used as the negative control and were considered to be 100%. After 10 min on ice, the cells were analyzed, immediately, by a four color FACSCalibur (Becton Dickinson, San Jose, CA, USA) flow cytometer. Forward and side scatter light was used to identify the neutrophils cell populations.

IL-6-, IL-10-and TNFα-Inducing Activity of CRGs and Ech on Human Blood Cells
Blood processing was performed using the procedure described by De Groote et al. [41]. Heparinated peripheral blood was diluted 1:5 in sterile Medium 199 (Sigma, St. Louis, MO, USA) with glutamine (300 mg L −1 ) (Gibco, Darmstadt, Germany) and gentamicin (50 µg ml −1 ). Diluted blood (0.1 mL) was incubated with the investigated samples, in saline (37 • C, 5% CO 2 ). The CRGs were added to obtain the final concentrations of 5, 10, and 20 µg mL −1 Ech (to 1 µg mL −1 ) and their complexes, to obtain final concentration values corresponding to the substances, separately. After 24 h, the supernatants were collected and frozen, followed by determining the cytokine content, using specific ELISA kits, according to the manufacture's protocol ("Cytokine", Saint-Petersburg, Russia).

xCELLigence System
Experiments on the xCELLigence system were conducted by means of the Real-Time Cell Analyzer Dual Plate (RTCA-DP) instrument (ACEA Bioscience, San Diego, CA, USA). The recommendations proposed by Ke et al. [42] and Sokolova et al. [35] were applied to study the effect of the samples on human intestinal epithelial cell monolayers.

Statistical Analysis
All data are presented as means ± standard deviations. Statistical calculation was conducted by ANOVA one-way analysis of variance. Differences were suggested when statistically probable at p < 0.01.

Conclusions
The inclusion of Ech into the carrageenan matrix enables a decrease the spermotoxicity of the Ech (besides protection of the substance from oxidation and improvement its solubility [11]), preserving its protective properties against the ROS synthesis by neutrophils, and the protective action towards the HT-29 intestinal epithelial cells.