Toxicity and Anti-Inflammatory Effects of IAgave sisalana/I Extract Derived from Agroindustrial Residue

Background: In several countries, the leaf juice of Agave sisalana (also known as sisal) is widely used topically, especially as an antiseptic, and orally for the treatment of different pathologies. However, in Brazil, which is the largest producer of Agave sisalana, its residue, which represents th...

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Veröffentlicht in:Plants (Basel) 2023-03, Vol.12 (7)
Hauptverfasser: Costa, Luisa Taynara Silvério da, Fracasso, Julia Amanda Rodrigues, Guarnier, Lucas Pires, Brito, Gustavo Reis de, Fumis, Daniel Baldini, Camargo Bittencourt, Renata Aparecida de, Guiotti, Aimée Maria, Barros Barbosa, Débora de, Camargo, Isabel Cristina Cherici, Souza, Edislane Barreiros de, Oliva Neto, Pedro de, Santos, Lucinéia dos
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container_issue 7
container_start_page
container_title Plants (Basel)
container_volume 12
creator Costa, Luisa Taynara Silvério da
Fracasso, Julia Amanda Rodrigues
Guarnier, Lucas Pires
Brito, Gustavo Reis de
Fumis, Daniel Baldini
Camargo Bittencourt, Renata Aparecida de
Guiotti, Aimée Maria
Barros Barbosa, Débora de
Camargo, Isabel Cristina Cherici
Souza, Edislane Barreiros de
Oliva Neto, Pedro de
Santos, Lucinéia dos
description Background: In several countries, the leaf juice of Agave sisalana (also known as sisal) is widely used topically, especially as an antiseptic, and orally for the treatment of different pathologies. However, in Brazil, which is the largest producer of Agave sisalana, its residue, which represents the majority of its weight, has been thrown away. For this reason, the determination of the pharmacological and toxicological potentials of sisal residue and its possible therapeutic use is seen as a way to contribute to the sustainable development and social promotion of the largest producer of sisal in Brazil, the interior of Bahia State, which is among the poorest areas in the country. Given the scarcity of available scientific studies on the pharmacological and toxicological properties of sisal residue juice, this study aimed to promote the acid hydrolysis of this juice to potentiate the anti-inflammatory effect already described in the literature. Furthermore, it aimed to evaluate the toxicological profile of the hydrolyzed extract (EAH) and to determine its acute toxicity, as well as its side effects on the reproductive aspects of rats. Method: The anti-inflammatory effect of EAH was evaluated in vitro using the induction of hemolysis by hypotonic solution and in vivo in rats using the carrageenan-induced paw edema test and the xylene-induced ear edema test. The acute toxicity, resulting from a single-dose administration, was investigated for some manifestation of toxic symptoms related to motor control and consciousness in rats. At a concentration of 100 mg/kg, by repeated doses, the reproductive toxicity effects of EAH in rats were assessed. Results: In vitro anti-inflammatory activity was positive using the human red blood cell membrane stabilization method. In both in vivo tests used to assess the anti-inflammatory activity, EAH (at three doses) significantly inhibited edema when compared to the control group. At a dose of 50 mg/kg, EAH exhibited a greater effect than indomethacin, a nonsteroidal anti-inflammatory drug with known activity. In vivo toxicological studies have shown that EAH does not present toxic effects when administered orally in a single dose, up to 1000 mg/kg. Finally, EAH promoted a gonadotoxic effect and increased the embryonic mortality rate after implantation. Conclusions: It is suggested that the anti-edematogenic effect of the acid hydrolysis extract from sisal juice is due to the high concentration of steroidal sapogenins. There
doi_str_mv 10.3390/plants12071523
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However, in Brazil, which is the largest producer of Agave sisalana, its residue, which represents the majority of its weight, has been thrown away. For this reason, the determination of the pharmacological and toxicological potentials of sisal residue and its possible therapeutic use is seen as a way to contribute to the sustainable development and social promotion of the largest producer of sisal in Brazil, the interior of Bahia State, which is among the poorest areas in the country. Given the scarcity of available scientific studies on the pharmacological and toxicological properties of sisal residue juice, this study aimed to promote the acid hydrolysis of this juice to potentiate the anti-inflammatory effect already described in the literature. Furthermore, it aimed to evaluate the toxicological profile of the hydrolyzed extract (EAH) and to determine its acute toxicity, as well as its side effects on the reproductive aspects of rats. Method: The anti-inflammatory effect of EAH was evaluated in vitro using the induction of hemolysis by hypotonic solution and in vivo in rats using the carrageenan-induced paw edema test and the xylene-induced ear edema test. The acute toxicity, resulting from a single-dose administration, was investigated for some manifestation of toxic symptoms related to motor control and consciousness in rats. At a concentration of 100 mg/kg, by repeated doses, the reproductive toxicity effects of EAH in rats were assessed. Results: In vitro anti-inflammatory activity was positive using the human red blood cell membrane stabilization method. In both in vivo tests used to assess the anti-inflammatory activity, EAH (at three doses) significantly inhibited edema when compared to the control group. At a dose of 50 mg/kg, EAH exhibited a greater effect than indomethacin, a nonsteroidal anti-inflammatory drug with known activity. In vivo toxicological studies have shown that EAH does not present toxic effects when administered orally in a single dose, up to 1000 mg/kg. Finally, EAH promoted a gonadotoxic effect and increased the embryonic mortality rate after implantation. Conclusions: It is suggested that the anti-edematogenic effect of the acid hydrolysis extract from sisal juice is due to the high concentration of steroidal sapogenins. Therefore, this extract can be considered a potential new anti-inflammatory or even an important sapogenin source for the development of steroidal glucocorticoids. However, further studies are needed to elucidate the chemical composition of sisal juice. 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However, in Brazil, which is the largest producer of Agave sisalana, its residue, which represents the majority of its weight, has been thrown away. For this reason, the determination of the pharmacological and toxicological potentials of sisal residue and its possible therapeutic use is seen as a way to contribute to the sustainable development and social promotion of the largest producer of sisal in Brazil, the interior of Bahia State, which is among the poorest areas in the country. Given the scarcity of available scientific studies on the pharmacological and toxicological properties of sisal residue juice, this study aimed to promote the acid hydrolysis of this juice to potentiate the anti-inflammatory effect already described in the literature. Furthermore, it aimed to evaluate the toxicological profile of the hydrolyzed extract (EAH) and to determine its acute toxicity, as well as its side effects on the reproductive aspects of rats. Method: The anti-inflammatory effect of EAH was evaluated in vitro using the induction of hemolysis by hypotonic solution and in vivo in rats using the carrageenan-induced paw edema test and the xylene-induced ear edema test. The acute toxicity, resulting from a single-dose administration, was investigated for some manifestation of toxic symptoms related to motor control and consciousness in rats. At a concentration of 100 mg/kg, by repeated doses, the reproductive toxicity effects of EAH in rats were assessed. Results: In vitro anti-inflammatory activity was positive using the human red blood cell membrane stabilization method. In both in vivo tests used to assess the anti-inflammatory activity, EAH (at three doses) significantly inhibited edema when compared to the control group. At a dose of 50 mg/kg, EAH exhibited a greater effect than indomethacin, a nonsteroidal anti-inflammatory drug with known activity. In vivo toxicological studies have shown that EAH does not present toxic effects when administered orally in a single dose, up to 1000 mg/kg. Finally, EAH promoted a gonadotoxic effect and increased the embryonic mortality rate after implantation. Conclusions: It is suggested that the anti-edematogenic effect of the acid hydrolysis extract from sisal juice is due to the high concentration of steroidal sapogenins. Therefore, this extract can be considered a potential new anti-inflammatory or even an important sapogenin source for the development of steroidal glucocorticoids. However, further studies are needed to elucidate the chemical composition of sisal juice. Regarding toxicology studies, EAH did not show cytotoxic and clastogenic potentials, but it presented a powerful reproductive toxic effect in rats.</description><subject>Anti-inflammatory drugs</subject><subject>Chemical properties</subject><subject>Corticosteroids</subject><subject>Pharmaceutical research</subject><subject>Sisal hemp</subject><issn>2223-7747</issn><issn>2223-7747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNptj0tLAzEQx4MoWGqvngOePGybx3aze1xq1YWCUOu5TJPJEtmHbNLSfnsjemjBmYEZht9_HoTcczaVsmCzrwa64Llgis-FvCIjIYRMlErV9Vl9Sybef7JoeQyejUi96Y9Ou3Ci0BladsElVWcbaFsI_XCiS2tRB097S6uyhgNS7zzEZTCr6PIYBtCBPuHgDmioHfqWlvXQu87sfRgcNHSN3pk93pEbC43HyV8ek4_n5WbxmqzeXqpFuUpqzrhIdpoXRmqhkReskIhMpIajgDRX2Y4jGhBcpEWRYfzTcD5XRmkxF4qBzHdCjsnD79waGty6zvY_J7bO622p0qxI87gmUtN_qOgGW6f7Dq2L_QvB44UgMgGPoYa999vqfX3OfgPS0XdF</recordid><startdate>20230301</startdate><enddate>20230301</enddate><creator>Costa, Luisa Taynara Silvério da</creator><creator>Fracasso, Julia Amanda Rodrigues</creator><creator>Guarnier, Lucas Pires</creator><creator>Brito, Gustavo Reis de</creator><creator>Fumis, Daniel Baldini</creator><creator>Camargo Bittencourt, Renata Aparecida de</creator><creator>Guiotti, Aimée Maria</creator><creator>Barros Barbosa, Débora de</creator><creator>Camargo, Isabel Cristina Cherici</creator><creator>Souza, Edislane Barreiros de</creator><creator>Oliva Neto, Pedro de</creator><creator>Santos, Lucinéia dos</creator><general>MDPI AG</general><scope>ISR</scope></search><sort><creationdate>20230301</creationdate><title>Toxicity and Anti-Inflammatory Effects of IAgave sisalana/I Extract Derived from Agroindustrial Residue</title><author>Costa, Luisa Taynara Silvério da ; Fracasso, Julia Amanda Rodrigues ; Guarnier, Lucas Pires ; Brito, Gustavo Reis de ; Fumis, Daniel Baldini ; Camargo Bittencourt, Renata Aparecida de ; Guiotti, Aimée Maria ; Barros Barbosa, Débora de ; Camargo, Isabel Cristina Cherici ; Souza, Edislane Barreiros de ; Oliva Neto, Pedro de ; Santos, Lucinéia dos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g1012-bc19d3c2ce19093ee024d1e2a4876b1eeda2124996e152d1157d7c25270a38b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Anti-inflammatory drugs</topic><topic>Chemical properties</topic><topic>Corticosteroids</topic><topic>Pharmaceutical research</topic><topic>Sisal hemp</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Costa, Luisa Taynara Silvério da</creatorcontrib><creatorcontrib>Fracasso, Julia Amanda Rodrigues</creatorcontrib><creatorcontrib>Guarnier, Lucas Pires</creatorcontrib><creatorcontrib>Brito, Gustavo Reis de</creatorcontrib><creatorcontrib>Fumis, Daniel Baldini</creatorcontrib><creatorcontrib>Camargo Bittencourt, Renata Aparecida de</creatorcontrib><creatorcontrib>Guiotti, Aimée Maria</creatorcontrib><creatorcontrib>Barros Barbosa, Débora de</creatorcontrib><creatorcontrib>Camargo, Isabel Cristina Cherici</creatorcontrib><creatorcontrib>Souza, Edislane Barreiros de</creatorcontrib><creatorcontrib>Oliva Neto, Pedro de</creatorcontrib><creatorcontrib>Santos, Lucinéia dos</creatorcontrib><collection>Gale In Context: Science</collection><jtitle>Plants (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Costa, Luisa Taynara Silvério da</au><au>Fracasso, Julia Amanda Rodrigues</au><au>Guarnier, Lucas Pires</au><au>Brito, Gustavo Reis de</au><au>Fumis, Daniel Baldini</au><au>Camargo Bittencourt, Renata Aparecida de</au><au>Guiotti, Aimée Maria</au><au>Barros Barbosa, Débora de</au><au>Camargo, Isabel Cristina Cherici</au><au>Souza, Edislane Barreiros de</au><au>Oliva Neto, Pedro de</au><au>Santos, Lucinéia dos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toxicity and Anti-Inflammatory Effects of IAgave sisalana/I Extract Derived from Agroindustrial Residue</atitle><jtitle>Plants (Basel)</jtitle><date>2023-03-01</date><risdate>2023</risdate><volume>12</volume><issue>7</issue><issn>2223-7747</issn><eissn>2223-7747</eissn><abstract>Background: In several countries, the leaf juice of Agave sisalana (also known as sisal) is widely used topically, especially as an antiseptic, and orally for the treatment of different pathologies. However, in Brazil, which is the largest producer of Agave sisalana, its residue, which represents the majority of its weight, has been thrown away. For this reason, the determination of the pharmacological and toxicological potentials of sisal residue and its possible therapeutic use is seen as a way to contribute to the sustainable development and social promotion of the largest producer of sisal in Brazil, the interior of Bahia State, which is among the poorest areas in the country. Given the scarcity of available scientific studies on the pharmacological and toxicological properties of sisal residue juice, this study aimed to promote the acid hydrolysis of this juice to potentiate the anti-inflammatory effect already described in the literature. Furthermore, it aimed to evaluate the toxicological profile of the hydrolyzed extract (EAH) and to determine its acute toxicity, as well as its side effects on the reproductive aspects of rats. Method: The anti-inflammatory effect of EAH was evaluated in vitro using the induction of hemolysis by hypotonic solution and in vivo in rats using the carrageenan-induced paw edema test and the xylene-induced ear edema test. The acute toxicity, resulting from a single-dose administration, was investigated for some manifestation of toxic symptoms related to motor control and consciousness in rats. At a concentration of 100 mg/kg, by repeated doses, the reproductive toxicity effects of EAH in rats were assessed. Results: In vitro anti-inflammatory activity was positive using the human red blood cell membrane stabilization method. In both in vivo tests used to assess the anti-inflammatory activity, EAH (at three doses) significantly inhibited edema when compared to the control group. At a dose of 50 mg/kg, EAH exhibited a greater effect than indomethacin, a nonsteroidal anti-inflammatory drug with known activity. In vivo toxicological studies have shown that EAH does not present toxic effects when administered orally in a single dose, up to 1000 mg/kg. Finally, EAH promoted a gonadotoxic effect and increased the embryonic mortality rate after implantation. Conclusions: It is suggested that the anti-edematogenic effect of the acid hydrolysis extract from sisal juice is due to the high concentration of steroidal sapogenins. Therefore, this extract can be considered a potential new anti-inflammatory or even an important sapogenin source for the development of steroidal glucocorticoids. However, further studies are needed to elucidate the chemical composition of sisal juice. Regarding toxicology studies, EAH did not show cytotoxic and clastogenic potentials, but it presented a powerful reproductive toxic effect in rats.</abstract><pub>MDPI AG</pub><doi>10.3390/plants12071523</doi></addata></record>
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source MDPI - Multidisciplinary Digital Publishing Institute; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; PubMed Central Open Access
subjects Anti-inflammatory drugs
Chemical properties
Corticosteroids
Pharmaceutical research
Sisal hemp
title Toxicity and Anti-Inflammatory Effects of IAgave sisalana/I Extract Derived from Agroindustrial Residue
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