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Effects of Artemisia macrocephala Jacquem on Memory Deficits and Brain Oxidative Stress in Streptozotocin-Induced Diabetic Mice

Different species of Artemisia have been reported to have therapeutic potential in treating various health disorders, including diabetes and memory dysfunction. The present study was planned to evaluate the effects of Artemisia macrocephala Jacquem crude extract and its subfractions as antiamnesic a...

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Autores principales: Bari, Atiqul, Shah, Syed Muhammad Mukarram, Al-Joufi, Fakhria A., Shah, Syed Wadood Ali, Shoaib, Mohammad, Shah, Ismail, Zahoor, Muhammad, Ahmed, Muhammad Naeem, Ghias, Mehreen, Shah, Syed Muhammad Hassan, Khalil, Atif Ali Khan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9028531/
https://www.ncbi.nlm.nih.gov/pubmed/35458597
http://dx.doi.org/10.3390/molecules27082399
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author Bari, Atiqul
Shah, Syed Muhammad Mukarram
Al-Joufi, Fakhria A.
Shah, Syed Wadood Ali
Shoaib, Mohammad
Shah, Ismail
Zahoor, Muhammad
Ahmed, Muhammad Naeem
Ghias, Mehreen
Shah, Syed Muhammad Hassan
Khalil, Atif Ali Khan
author_facet Bari, Atiqul
Shah, Syed Muhammad Mukarram
Al-Joufi, Fakhria A.
Shah, Syed Wadood Ali
Shoaib, Mohammad
Shah, Ismail
Zahoor, Muhammad
Ahmed, Muhammad Naeem
Ghias, Mehreen
Shah, Syed Muhammad Hassan
Khalil, Atif Ali Khan
author_sort Bari, Atiqul
collection PubMed
description Different species of Artemisia have been reported to have therapeutic potential in treating various health disorders, including diabetes and memory dysfunction. The present study was planned to evaluate the effects of Artemisia macrocephala Jacquem crude extract and its subfractions as antiamnesic agents in streptozotocin-induced (STZ) diabetic mice. The in vivo behavioral studies were performed using the Y Maze test and novel object recognition test (NORT) test at doses of 100 and 200 mg/kg of crude extract and 75 and 150 mg/kg of fractions. The in vitro and ex vivo anticholinesterase activities, along with biochemical parameters (superoxide dismutase, catalase, glutathione and lipid peroxidation) in the brain, were evaluated. Blood glucose levels were monitored with a glucometer; crude extract and fractions reduced the glucose level considerably, with some differences in the extent of their efficacies. The crude extract and fractions demonstrated significant inhibitory activity against cholinesterases (AChE and BuChE) in vitro. Crude, chloroform and ethyl acetate extract were found to be more potent than the other fractions, with IC(50) of Crd-Am = 116.36 ± 1.48 and 240.52 ± 1.35 µg/mL, Chl-Am = 52.68 ± 1.09 and 57.45 ± 1.39 µg/mL and Et-Am = 75.19 ± 1.02 and 116.58 ± 1.09 µg/mL, respectively. Oxidative stress biomarkers like superoxide dismutase, catalase and glutathione levels were elevated, whereas MDA levels were reduced by crude extract and all fractions with little difference in their respective values. The Y-maze test and novel object recognition test demonstrated declines in memory impairment in groups (n = 6) treated with crude extract and fractions as compared to STZ diabetic (amnesic) group. The most active fraction, Chl-Am, was also subjected to isolation of bioactive compounds; three compounds were obtained in pure state and designated as AB-I, AB-II and AB-III. Overall, the results of the study showed that Artemisia macrocephala Jacquem enhanced the memory impairment associated with diabetes, elevated acetylcholine levels and ameliorated oxidative stress. Further studies are needed to explore the beneficial role of the secondary metabolites isolated in the present study as memory enhancers. Toxicological aspects of the extracts are also important and need to be evaluated in other animal models.
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spelling pubmed-90285312022-04-23 Effects of Artemisia macrocephala Jacquem on Memory Deficits and Brain Oxidative Stress in Streptozotocin-Induced Diabetic Mice Bari, Atiqul Shah, Syed Muhammad Mukarram Al-Joufi, Fakhria A. Shah, Syed Wadood Ali Shoaib, Mohammad Shah, Ismail Zahoor, Muhammad Ahmed, Muhammad Naeem Ghias, Mehreen Shah, Syed Muhammad Hassan Khalil, Atif Ali Khan Molecules Article Different species of Artemisia have been reported to have therapeutic potential in treating various health disorders, including diabetes and memory dysfunction. The present study was planned to evaluate the effects of Artemisia macrocephala Jacquem crude extract and its subfractions as antiamnesic agents in streptozotocin-induced (STZ) diabetic mice. The in vivo behavioral studies were performed using the Y Maze test and novel object recognition test (NORT) test at doses of 100 and 200 mg/kg of crude extract and 75 and 150 mg/kg of fractions. The in vitro and ex vivo anticholinesterase activities, along with biochemical parameters (superoxide dismutase, catalase, glutathione and lipid peroxidation) in the brain, were evaluated. Blood glucose levels were monitored with a glucometer; crude extract and fractions reduced the glucose level considerably, with some differences in the extent of their efficacies. The crude extract and fractions demonstrated significant inhibitory activity against cholinesterases (AChE and BuChE) in vitro. Crude, chloroform and ethyl acetate extract were found to be more potent than the other fractions, with IC(50) of Crd-Am = 116.36 ± 1.48 and 240.52 ± 1.35 µg/mL, Chl-Am = 52.68 ± 1.09 and 57.45 ± 1.39 µg/mL and Et-Am = 75.19 ± 1.02 and 116.58 ± 1.09 µg/mL, respectively. Oxidative stress biomarkers like superoxide dismutase, catalase and glutathione levels were elevated, whereas MDA levels were reduced by crude extract and all fractions with little difference in their respective values. The Y-maze test and novel object recognition test demonstrated declines in memory impairment in groups (n = 6) treated with crude extract and fractions as compared to STZ diabetic (amnesic) group. The most active fraction, Chl-Am, was also subjected to isolation of bioactive compounds; three compounds were obtained in pure state and designated as AB-I, AB-II and AB-III. Overall, the results of the study showed that Artemisia macrocephala Jacquem enhanced the memory impairment associated with diabetes, elevated acetylcholine levels and ameliorated oxidative stress. Further studies are needed to explore the beneficial role of the secondary metabolites isolated in the present study as memory enhancers. Toxicological aspects of the extracts are also important and need to be evaluated in other animal models. MDPI 2022-04-08 /pmc/articles/PMC9028531/ /pubmed/35458597 http://dx.doi.org/10.3390/molecules27082399 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bari, Atiqul
Shah, Syed Muhammad Mukarram
Al-Joufi, Fakhria A.
Shah, Syed Wadood Ali
Shoaib, Mohammad
Shah, Ismail
Zahoor, Muhammad
Ahmed, Muhammad Naeem
Ghias, Mehreen
Shah, Syed Muhammad Hassan
Khalil, Atif Ali Khan
Effects of Artemisia macrocephala Jacquem on Memory Deficits and Brain Oxidative Stress in Streptozotocin-Induced Diabetic Mice
title Effects of Artemisia macrocephala Jacquem on Memory Deficits and Brain Oxidative Stress in Streptozotocin-Induced Diabetic Mice
title_full Effects of Artemisia macrocephala Jacquem on Memory Deficits and Brain Oxidative Stress in Streptozotocin-Induced Diabetic Mice
title_fullStr Effects of Artemisia macrocephala Jacquem on Memory Deficits and Brain Oxidative Stress in Streptozotocin-Induced Diabetic Mice
title_full_unstemmed Effects of Artemisia macrocephala Jacquem on Memory Deficits and Brain Oxidative Stress in Streptozotocin-Induced Diabetic Mice
title_short Effects of Artemisia macrocephala Jacquem on Memory Deficits and Brain Oxidative Stress in Streptozotocin-Induced Diabetic Mice
title_sort effects of artemisia macrocephala jacquem on memory deficits and brain oxidative stress in streptozotocin-induced diabetic mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9028531/
https://www.ncbi.nlm.nih.gov/pubmed/35458597
http://dx.doi.org/10.3390/molecules27082399
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