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Article: Tylophora hirsuta L. leaf extract attenuates alloxan-induced diabetes in mice by suppressing oxidative stress and α-amylase

TitleTylophora hirsuta L. leaf extract attenuates alloxan-induced diabetes in mice by suppressing oxidative stress and α-amylase
Authors
KeywordsTylophora hirsuta
Diabetes mellitus
Oxidative stress
Alpha-amylase
Phenolic compounds
Issue Date2021
PublisherWolters Kluwer - Medknow Publications and Media Pvt. Ltd. The Journal's web site is located at http://www.apjtb.org
Citation
Asian Pacific Journal of Tropical Biomedicine, 2021, v. 11 n. 9, p. 394-404 How to Cite?
AbstractObjective: To evaluate the antidiabetic potential of leaf extracts of Tylophora hirsuta (T. hirsuta). Methods: The methanolic and ethyl acetate extracts of T. hirsuta leaves were analyzed by high pressure liquid chromatography. In vitro antioxidant activity was determined by ferric ion reduction, 1, 1-diphenyl-2-picrylhydrazyl, and hydrogen peroxide scavenging methods. In vitro alpha amylase (α-amylase) inhibitory activity of the plant extracts was assessed. In vivo antidiabetic potential was determined in alloxan-induced diabetic mice to assess glycated hemoglobin (HbA1c), oral glucose tolerance, serum amylase, lipid profile, fasting blood glucose, and body weight. Histopathological lesions of the pancreas, liver and kidney were observed. Oxidative stress biomarkers such as superoxide dismutase, catalase and peroxidase were also determined. Results: Quercetin, chlorogenic acid, p-coumaric acid, and m-coumaric acid were found in the plant extracts. The methanolic plant extract exhibited higher in vitro antioxidant activities than the ethyl acetate extract. Moreover, methanolic plant extract exhibited (83.90±1.56)% α-amylase inhibitory activity at 3.2 mg/ mL concentration. Animal study showed that the methanolic extract of T. hirsuta improved the levels of fasting blood glucose, HbA1c, serum α-amylase, lipid profile, liver function biomarkers, and kidney functions of diabetic mice. Moreover, the methanolic extract ameliorated diabetes-related oxidative stress by increasing superoxide dismutase and catalase activities and decreasing peroxidase and malondialdehyde levels. Histopathological examination showed that the plant extract had improved the integrity of pancreatic islets of Langerhans and reduced the pathological lesions in the liver and kidney of diabetic mice. Conclusions: The methanolic extract of T. hirsuta exhibits pronounced antidiabetic activity in mice through reduction of oxidative stress. The plant extract has several natural antioxidants such as phenolic acids. T. hirsuta extract could serve as a nutraceutical for managing diabetes mellitus.
Persistent Identifierhttp://hdl.handle.net/10722/301625
ISSN
2021 Impact Factor: 1.514
2020 SCImago Journal Rankings: 0.507
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorAkhtar, MF-
dc.contributor.authorShagufta, A-
dc.contributor.authorSaleem, A-
dc.contributor.authorBaig, MMFA-
dc.contributor.authorSharif, A-
dc.contributor.authorRasul, A-
dc.contributor.authorAbdel-Daim, MM-
dc.date.accessioned2021-08-09T03:41:48Z-
dc.date.available2021-08-09T03:41:48Z-
dc.date.issued2021-
dc.identifier.citationAsian Pacific Journal of Tropical Biomedicine, 2021, v. 11 n. 9, p. 394-404-
dc.identifier.issn2221-1691-
dc.identifier.urihttp://hdl.handle.net/10722/301625-
dc.description.abstractObjective: To evaluate the antidiabetic potential of leaf extracts of Tylophora hirsuta (T. hirsuta). Methods: The methanolic and ethyl acetate extracts of T. hirsuta leaves were analyzed by high pressure liquid chromatography. In vitro antioxidant activity was determined by ferric ion reduction, 1, 1-diphenyl-2-picrylhydrazyl, and hydrogen peroxide scavenging methods. In vitro alpha amylase (α-amylase) inhibitory activity of the plant extracts was assessed. In vivo antidiabetic potential was determined in alloxan-induced diabetic mice to assess glycated hemoglobin (HbA1c), oral glucose tolerance, serum amylase, lipid profile, fasting blood glucose, and body weight. Histopathological lesions of the pancreas, liver and kidney were observed. Oxidative stress biomarkers such as superoxide dismutase, catalase and peroxidase were also determined. Results: Quercetin, chlorogenic acid, p-coumaric acid, and m-coumaric acid were found in the plant extracts. The methanolic plant extract exhibited higher in vitro antioxidant activities than the ethyl acetate extract. Moreover, methanolic plant extract exhibited (83.90±1.56)% α-amylase inhibitory activity at 3.2 mg/ mL concentration. Animal study showed that the methanolic extract of T. hirsuta improved the levels of fasting blood glucose, HbA1c, serum α-amylase, lipid profile, liver function biomarkers, and kidney functions of diabetic mice. Moreover, the methanolic extract ameliorated diabetes-related oxidative stress by increasing superoxide dismutase and catalase activities and decreasing peroxidase and malondialdehyde levels. Histopathological examination showed that the plant extract had improved the integrity of pancreatic islets of Langerhans and reduced the pathological lesions in the liver and kidney of diabetic mice. Conclusions: The methanolic extract of T. hirsuta exhibits pronounced antidiabetic activity in mice through reduction of oxidative stress. The plant extract has several natural antioxidants such as phenolic acids. T. hirsuta extract could serve as a nutraceutical for managing diabetes mellitus.-
dc.languageeng-
dc.publisherWolters Kluwer - Medknow Publications and Media Pvt. Ltd. The Journal's web site is located at http://www.apjtb.org-
dc.relation.ispartofAsian Pacific Journal of Tropical Biomedicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectTylophora hirsuta-
dc.subjectDiabetes mellitus-
dc.subjectOxidative stress-
dc.subjectAlpha-amylase-
dc.subjectPhenolic compounds-
dc.titleTylophora hirsuta L. leaf extract attenuates alloxan-induced diabetes in mice by suppressing oxidative stress and α-amylase-
dc.typeArticle-
dc.identifier.emailBaig, MMFA: faran@hku.hk-
dc.identifier.authorityBaig, MMFA=rp02755-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.4103/2221-1691.321128-
dc.identifier.scopuseid_2-s2.0-85111731865-
dc.identifier.hkuros323987-
dc.identifier.volume11-
dc.identifier.issue9-
dc.identifier.spage394-
dc.identifier.epage404-
dc.identifier.isiWOS:000678618100003-
dc.publisher.placeIndia-

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