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Pharmacological and pharmacognostical valuation of Canna indica leaves extract by quantifying safety profile and neuroprotective potential

The current study primarily focused on the pharmacognostical and phytochemical screening of Canna indica and further analyzing the leaves extract for toxicological profile and neuroprotective potential. The microscopic, dry powder properties of the leaf material and phytochemical, physicochemical an...

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Autores principales: Chigurupati, Sridevi, Abdul Rahman Alharbi, Nouf, Sharma, Arun Kumar, Alhowail, Ahmad, Vardharajula, Venkata Ramaiah, Vijayabalan, Shantini, Das, Suprava, Kauser, Fatema, Amin, Elham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459113/
https://www.ncbi.nlm.nih.gov/pubmed/34588868
http://dx.doi.org/10.1016/j.sjbs.2021.05.072
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author Chigurupati, Sridevi
Abdul Rahman Alharbi, Nouf
Sharma, Arun Kumar
Alhowail, Ahmad
Vardharajula, Venkata Ramaiah
Vijayabalan, Shantini
Das, Suprava
Kauser, Fatema
Amin, Elham
author_facet Chigurupati, Sridevi
Abdul Rahman Alharbi, Nouf
Sharma, Arun Kumar
Alhowail, Ahmad
Vardharajula, Venkata Ramaiah
Vijayabalan, Shantini
Das, Suprava
Kauser, Fatema
Amin, Elham
author_sort Chigurupati, Sridevi
collection PubMed
description The current study primarily focused on the pharmacognostical and phytochemical screening of Canna indica and further analyzing the leaves extract for toxicological profile and neuroprotective potential. The microscopic, dry powder properties of the leaf material and phytochemical, physicochemical analysis was evaluated for pharmacognostical assessment. Dry leaves of C. indica were extracted using methanol and then further studied for both in vitro and in vivo toxicological study. The acute toxicity was measured by estimating the antioxidant defense system and anatomical impairment in the rat's organs. Also, the neuroprotective activity of the plant extract was assessed using anticholinesterase enzymatic inhibitory assay. The extract was found to be hemocompatible and showed absences of induction of behavioural changes. Likewise, no changes were seen on the anatomical structure of the rat’s organs. The methanolic extract portrayed a significant upsurge in the reduced glutathione level and showed a comparable acetylcholinesterase inhibition in a dosedependent manner with an IC50 value of 14.53 μg/mL compared to the standard Donepezil with an IC50 value of 13.31 μg/mL. C. indica has compelling pharmacognostical characteristics, good safety reports, and significant antioxidant as well as the neuroprotective potential that shows great potential for its further in-depth research for pharmacological use.
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spelling pubmed-84591132021-09-28 Pharmacological and pharmacognostical valuation of Canna indica leaves extract by quantifying safety profile and neuroprotective potential Chigurupati, Sridevi Abdul Rahman Alharbi, Nouf Sharma, Arun Kumar Alhowail, Ahmad Vardharajula, Venkata Ramaiah Vijayabalan, Shantini Das, Suprava Kauser, Fatema Amin, Elham Saudi J Biol Sci Original Article The current study primarily focused on the pharmacognostical and phytochemical screening of Canna indica and further analyzing the leaves extract for toxicological profile and neuroprotective potential. The microscopic, dry powder properties of the leaf material and phytochemical, physicochemical analysis was evaluated for pharmacognostical assessment. Dry leaves of C. indica were extracted using methanol and then further studied for both in vitro and in vivo toxicological study. The acute toxicity was measured by estimating the antioxidant defense system and anatomical impairment in the rat's organs. Also, the neuroprotective activity of the plant extract was assessed using anticholinesterase enzymatic inhibitory assay. The extract was found to be hemocompatible and showed absences of induction of behavioural changes. Likewise, no changes were seen on the anatomical structure of the rat’s organs. The methanolic extract portrayed a significant upsurge in the reduced glutathione level and showed a comparable acetylcholinesterase inhibition in a dosedependent manner with an IC50 value of 14.53 μg/mL compared to the standard Donepezil with an IC50 value of 13.31 μg/mL. C. indica has compelling pharmacognostical characteristics, good safety reports, and significant antioxidant as well as the neuroprotective potential that shows great potential for its further in-depth research for pharmacological use. Elsevier 2021-10 2021-06-01 /pmc/articles/PMC8459113/ /pubmed/34588868 http://dx.doi.org/10.1016/j.sjbs.2021.05.072 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Chigurupati, Sridevi
Abdul Rahman Alharbi, Nouf
Sharma, Arun Kumar
Alhowail, Ahmad
Vardharajula, Venkata Ramaiah
Vijayabalan, Shantini
Das, Suprava
Kauser, Fatema
Amin, Elham
Pharmacological and pharmacognostical valuation of Canna indica leaves extract by quantifying safety profile and neuroprotective potential
title Pharmacological and pharmacognostical valuation of Canna indica leaves extract by quantifying safety profile and neuroprotective potential
title_full Pharmacological and pharmacognostical valuation of Canna indica leaves extract by quantifying safety profile and neuroprotective potential
title_fullStr Pharmacological and pharmacognostical valuation of Canna indica leaves extract by quantifying safety profile and neuroprotective potential
title_full_unstemmed Pharmacological and pharmacognostical valuation of Canna indica leaves extract by quantifying safety profile and neuroprotective potential
title_short Pharmacological and pharmacognostical valuation of Canna indica leaves extract by quantifying safety profile and neuroprotective potential
title_sort pharmacological and pharmacognostical valuation of canna indica leaves extract by quantifying safety profile and neuroprotective potential
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459113/
https://www.ncbi.nlm.nih.gov/pubmed/34588868
http://dx.doi.org/10.1016/j.sjbs.2021.05.072
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