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In Vivo and In Silico Studies of Flavonoids Isolated from Pistacia integerrima as Potential Antidiarrheal Agents

[Image: see text] Pistacia integerrima leaf galls are used in several traditional medicines to cure many diseases such as diarrhea, asthma, fever, cough, vomiting, and hepatitis. The main goal of the present investigation was to assess the antidiarrheal effect of the Pistacia integerrima extracts/fr...

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Autores principales: Alhumaydhi, Fahad A., Rauf, Abdur, Rashid, Umer, Bawazeer, Saud, Khan, Khalid, Mubarak, Mohammad S., Aljohani, Abdullah S. M., Khan, Haroon, El-Saber Batiha, Gaber, El-Esawi, Mohamed A., Mishra, Abhay P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223227/
https://www.ncbi.nlm.nih.gov/pubmed/34179606
http://dx.doi.org/10.1021/acsomega.1c00298
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author Alhumaydhi, Fahad A.
Rauf, Abdur
Rashid, Umer
Bawazeer, Saud
Khan, Khalid
Mubarak, Mohammad S.
Aljohani, Abdullah S. M.
Khan, Haroon
El-Saber Batiha, Gaber
El-Esawi, Mohamed A.
Mishra, Abhay P.
author_facet Alhumaydhi, Fahad A.
Rauf, Abdur
Rashid, Umer
Bawazeer, Saud
Khan, Khalid
Mubarak, Mohammad S.
Aljohani, Abdullah S. M.
Khan, Haroon
El-Saber Batiha, Gaber
El-Esawi, Mohamed A.
Mishra, Abhay P.
author_sort Alhumaydhi, Fahad A.
collection PubMed
description [Image: see text] Pistacia integerrima leaf galls are used in several traditional medicines to cure many diseases such as diarrhea, asthma, fever, cough, vomiting, and hepatitis. The main goal of the present investigation was to assess the antidiarrheal effect of the Pistacia integerrima extracts/fractions and four isolated flavonoid compounds (1–4) on mice. An in vivo assay involving castor-oil-induced diarrhea was used to evaluate the antidiarrheal potential of extracts/fractions at 100, 200, and 400 mg/kg p.o., as well as isolated compounds at 5, 10, and 20 mg/kg p.o. Pretreatment of mice with extracts/fractions significantly attenuated castor-oil-induced diarrhea in a dose-dependent manner. Among all crude extracts and fractions, the ethyl acetate extract was the most effective with 100% protection against diarrhea followed by chloroform (75% protection) at 400 mg/kg p.o. Although all the isolated compounds exhibited strong antidiarrheal activity, isolated compounds 1 and 4 demonstrated 100% protection against diarrhea. Moreover, docking models were performed using the Molecular Operating Environment (MOE) and AutoDock software and suggested that the extracts and isolated compounds exert antidiarrheal activity by inhibiting mu-opioid and delta-opioid receptors. Therefore, our finding affords a strong pharmacological basis for the traditional use of P. integerrima galls in the treatment of diarrhea.
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spelling pubmed-82232272021-06-25 In Vivo and In Silico Studies of Flavonoids Isolated from Pistacia integerrima as Potential Antidiarrheal Agents Alhumaydhi, Fahad A. Rauf, Abdur Rashid, Umer Bawazeer, Saud Khan, Khalid Mubarak, Mohammad S. Aljohani, Abdullah S. M. Khan, Haroon El-Saber Batiha, Gaber El-Esawi, Mohamed A. Mishra, Abhay P. ACS Omega [Image: see text] Pistacia integerrima leaf galls are used in several traditional medicines to cure many diseases such as diarrhea, asthma, fever, cough, vomiting, and hepatitis. The main goal of the present investigation was to assess the antidiarrheal effect of the Pistacia integerrima extracts/fractions and four isolated flavonoid compounds (1–4) on mice. An in vivo assay involving castor-oil-induced diarrhea was used to evaluate the antidiarrheal potential of extracts/fractions at 100, 200, and 400 mg/kg p.o., as well as isolated compounds at 5, 10, and 20 mg/kg p.o. Pretreatment of mice with extracts/fractions significantly attenuated castor-oil-induced diarrhea in a dose-dependent manner. Among all crude extracts and fractions, the ethyl acetate extract was the most effective with 100% protection against diarrhea followed by chloroform (75% protection) at 400 mg/kg p.o. Although all the isolated compounds exhibited strong antidiarrheal activity, isolated compounds 1 and 4 demonstrated 100% protection against diarrhea. Moreover, docking models were performed using the Molecular Operating Environment (MOE) and AutoDock software and suggested that the extracts and isolated compounds exert antidiarrheal activity by inhibiting mu-opioid and delta-opioid receptors. Therefore, our finding affords a strong pharmacological basis for the traditional use of P. integerrima galls in the treatment of diarrhea. American Chemical Society 2021-06-14 /pmc/articles/PMC8223227/ /pubmed/34179606 http://dx.doi.org/10.1021/acsomega.1c00298 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Alhumaydhi, Fahad A.
Rauf, Abdur
Rashid, Umer
Bawazeer, Saud
Khan, Khalid
Mubarak, Mohammad S.
Aljohani, Abdullah S. M.
Khan, Haroon
El-Saber Batiha, Gaber
El-Esawi, Mohamed A.
Mishra, Abhay P.
In Vivo and In Silico Studies of Flavonoids Isolated from Pistacia integerrima as Potential Antidiarrheal Agents
title In Vivo and In Silico Studies of Flavonoids Isolated from Pistacia integerrima as Potential Antidiarrheal Agents
title_full In Vivo and In Silico Studies of Flavonoids Isolated from Pistacia integerrima as Potential Antidiarrheal Agents
title_fullStr In Vivo and In Silico Studies of Flavonoids Isolated from Pistacia integerrima as Potential Antidiarrheal Agents
title_full_unstemmed In Vivo and In Silico Studies of Flavonoids Isolated from Pistacia integerrima as Potential Antidiarrheal Agents
title_short In Vivo and In Silico Studies of Flavonoids Isolated from Pistacia integerrima as Potential Antidiarrheal Agents
title_sort in vivo and in silico studies of flavonoids isolated from pistacia integerrima as potential antidiarrheal agents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223227/
https://www.ncbi.nlm.nih.gov/pubmed/34179606
http://dx.doi.org/10.1021/acsomega.1c00298
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