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Anti-glycation properties of Illicium verum Hook. f. fruit in-vitro and in a diabetic rat model

BACKGROUND: Chronic hyperglycemic triggers the non-enzymatic glycation of biomolecules, resulting in the production of advanced glycation endproducts, that lead to several micro- and macrovascular complications. Therefore, the discovery of new, effective, and safe anti-glycation agents is an importa...

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Autores principales: Khan, Hafiz Nadeem, Rasheed, Saima, Choudhary, M. Iqbal, Ahmed, Nessar, Adem, Abdu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934496/
https://www.ncbi.nlm.nih.gov/pubmed/35305622
http://dx.doi.org/10.1186/s12906-022-03550-z
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author Khan, Hafiz Nadeem
Rasheed, Saima
Choudhary, M. Iqbal
Ahmed, Nessar
Adem, Abdu
author_facet Khan, Hafiz Nadeem
Rasheed, Saima
Choudhary, M. Iqbal
Ahmed, Nessar
Adem, Abdu
author_sort Khan, Hafiz Nadeem
collection PubMed
description BACKGROUND: Chronic hyperglycemic triggers the non-enzymatic glycation of biomolecules, resulting in the production of advanced glycation endproducts, that lead to several micro- and macrovascular complications. Therefore, the discovery of new, effective, and safe anti-glycation agents is an important need. One of the best choices for the management of diabetes is to use complementary and alternative medicinal therapies. Therefore, the present study was designed to evaluate the anti-glycation activity of ethanolic extract of Illicium verum Hook. f. (Star anise, a frequently used spice and medicinally important herb). METHODS: The anti-glycation activity of ethanolic extract of Illicium verum Hook. f. was determined by using both in-vitro and in-vivo assays. HSA-fructose glycation model was employed to assess the in-vitro inhibition of protein glycation, additionally cross-linked AGEs (formed by incubating lysozyme with fructose) were assessed by SDS polyacrylamide gel electrophoresis. Dual inhibitory mechanisms, i.e., antioxidant and metal chelating activities, were also evaluated by using DPPH, ABTS, and Fe (II)-chelation assays. Acute toxicity of I. verum extract was also performed (by administrating different doses i.e. 2,000, 1,500, 1,000, and 500 mg/kg of body weight). Finally, in-vivo anti-glycation potential was evaluated by 7 weeks of administration of I. verum extract in streptozotocin-induced diabetic rats. RESULTS: In HSA-fructose glycation model, extract of I. verum showed a good inhibitory activity with IC(50) value of 0.11±0.001 mg/mL, as compared to the standard inhibitor, rutin (IC(50) = 0.02±0.01 mg/mL). Extract of I. verum showed inhibitory activity in DPPH, and ABTS radical scavenging assays with IC(50) values of 130±1.0, and 57±2.0 μg/mL, respectively, while it was found to be inactive in the Fe(+2)-chelation assay. The extract was found to be non-toxic, and reduce the elevated blood glucose, urea, lipid, liver function parameters, and renal AGEs levels in streptozotocin-induced diabetic rats. CONCLUSIONS: These results suggest that I. verum supplementation might help to reduce the burden of AGEs, and may have potential in preventing diabetes-associated complications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-022-03550-z.
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spelling pubmed-89344962022-03-23 Anti-glycation properties of Illicium verum Hook. f. fruit in-vitro and in a diabetic rat model Khan, Hafiz Nadeem Rasheed, Saima Choudhary, M. Iqbal Ahmed, Nessar Adem, Abdu BMC Complement Med Ther Research BACKGROUND: Chronic hyperglycemic triggers the non-enzymatic glycation of biomolecules, resulting in the production of advanced glycation endproducts, that lead to several micro- and macrovascular complications. Therefore, the discovery of new, effective, and safe anti-glycation agents is an important need. One of the best choices for the management of diabetes is to use complementary and alternative medicinal therapies. Therefore, the present study was designed to evaluate the anti-glycation activity of ethanolic extract of Illicium verum Hook. f. (Star anise, a frequently used spice and medicinally important herb). METHODS: The anti-glycation activity of ethanolic extract of Illicium verum Hook. f. was determined by using both in-vitro and in-vivo assays. HSA-fructose glycation model was employed to assess the in-vitro inhibition of protein glycation, additionally cross-linked AGEs (formed by incubating lysozyme with fructose) were assessed by SDS polyacrylamide gel electrophoresis. Dual inhibitory mechanisms, i.e., antioxidant and metal chelating activities, were also evaluated by using DPPH, ABTS, and Fe (II)-chelation assays. Acute toxicity of I. verum extract was also performed (by administrating different doses i.e. 2,000, 1,500, 1,000, and 500 mg/kg of body weight). Finally, in-vivo anti-glycation potential was evaluated by 7 weeks of administration of I. verum extract in streptozotocin-induced diabetic rats. RESULTS: In HSA-fructose glycation model, extract of I. verum showed a good inhibitory activity with IC(50) value of 0.11±0.001 mg/mL, as compared to the standard inhibitor, rutin (IC(50) = 0.02±0.01 mg/mL). Extract of I. verum showed inhibitory activity in DPPH, and ABTS radical scavenging assays with IC(50) values of 130±1.0, and 57±2.0 μg/mL, respectively, while it was found to be inactive in the Fe(+2)-chelation assay. The extract was found to be non-toxic, and reduce the elevated blood glucose, urea, lipid, liver function parameters, and renal AGEs levels in streptozotocin-induced diabetic rats. CONCLUSIONS: These results suggest that I. verum supplementation might help to reduce the burden of AGEs, and may have potential in preventing diabetes-associated complications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-022-03550-z. BioMed Central 2022-03-19 /pmc/articles/PMC8934496/ /pubmed/35305622 http://dx.doi.org/10.1186/s12906-022-03550-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Khan, Hafiz Nadeem
Rasheed, Saima
Choudhary, M. Iqbal
Ahmed, Nessar
Adem, Abdu
Anti-glycation properties of Illicium verum Hook. f. fruit in-vitro and in a diabetic rat model
title Anti-glycation properties of Illicium verum Hook. f. fruit in-vitro and in a diabetic rat model
title_full Anti-glycation properties of Illicium verum Hook. f. fruit in-vitro and in a diabetic rat model
title_fullStr Anti-glycation properties of Illicium verum Hook. f. fruit in-vitro and in a diabetic rat model
title_full_unstemmed Anti-glycation properties of Illicium verum Hook. f. fruit in-vitro and in a diabetic rat model
title_short Anti-glycation properties of Illicium verum Hook. f. fruit in-vitro and in a diabetic rat model
title_sort anti-glycation properties of illicium verum hook. f. fruit in-vitro and in a diabetic rat model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934496/
https://www.ncbi.nlm.nih.gov/pubmed/35305622
http://dx.doi.org/10.1186/s12906-022-03550-z
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