Open Access
AMP kinase: A promising therapeutic drug target for post-COVID-19 complications
Mohammad Saquib Ashraf
1
,
Kanika Tuli
2, 3
,
Shadman Moiz
4
,
Satish Kumar Sharma
5
,
Sushila Sharma
6
,
Deepa Sharma
7
,
2
Guru Nanak Institute of Pharmacy, Dalewal, Hoshiarpur 144208, Punjab, India.
|
3
Guru Nanak Institute of Pharmacy, Dalewal, Hoshiarpur 144208, Punjab, India
|
4
Department of Biotechnology, Lalit Narayan Mithila University, Darbhanga 846004, Bihar, India.
|
5
Department of Pharmacology, Glocal School of Pharmacy, The Glocal University, Saharanpur, India
|
6
Department of Pharmacology, Glocal School of Pharmacy, The Glocal University, Saharanpur, India.
|
7
UMM Matrix Innovations Private Limited, Delhi 110044, India.
|
Publication type: Journal Article
Publication date: 2024-12-01
scimago Q1
wos Q1
SJR: 1.315
CiteScore: 10.9
Impact factor: 5.1
ISSN: 00243205, 18790631
PubMed ID:
39489398
Abstract
The COVID-19 pandemic, caused by SARS-CoV-2, has resulted in severe respiratory issues and persistent complications, particularly affecting glucose metabolism. Patients with or without pre-existing diabetes often experience worsened symptoms, highlighting the need for innovative therapeutic approaches. AMPK, a crucial regulator of cellular energy balance, plays a pivotal role in glucose metabolism, insulin sensitivity, and inflammatory responses. AMPK activation, through allosteric or kinase-dependent mechanisms, impacts cellular processes like glucose uptake, fatty acid oxidation, and autophagy. The tissue-specific distribution of AMPK emphasizes its role in maintaining metabolic homeostasis throughout the body. Intriguingly, SARS-CoV-2 infection inhibits AMPK, contributing to metabolic dysregulation and post-COVID-19 complications. AMPK activators like capsaicinoids, curcumin, phytoestrogens, cilostazol, and momordicosides have demonstrated the potential to regulate AMPK activity. Compounds from various sources improve fatty acid oxidation and insulin sensitivity, with metformin showing opposing effects on AMPK activation compared to the virus, suggesting potential therapeutic options. The diverse effects of AMPK activation extend to its role in countering viral infections, further highlighting its significance in COVID-19. This review explores AMPK activation mechanisms, its role in metabolic disorders, and the potential use of natural compounds to target AMPK for post-COVID-19 complications. Also, it aims to review the possible methods of activating AMPK to prevent post-COVID-19 diabetes and cardiovascular complications. It also explores the use of natural compounds for their therapeutic effects in targeting the AMPK pathways. Targeting AMPK activation emerges as a promising avenue to mitigate the long-term effects of COVID-19, offering hope for improved patient outcomes and a better quality of life.
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GOST
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Ashraf M. S. et al. AMP kinase: A promising therapeutic drug target for post-COVID-19 complications // Life Sciences. 2024. Vol. 359. p. 123202.
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Ashraf M. S., Tuli K., Moiz S., Sharma S. K., Sharma S., Sharma D., Adnan M. AMP kinase: A promising therapeutic drug target for post-COVID-19 complications // Life Sciences. 2024. Vol. 359. p. 123202.
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TY - JOUR
DO - 10.1016/j.lfs.2024.123202
UR - https://linkinghub.elsevier.com/retrieve/pii/S0024320524007926
TI - AMP kinase: A promising therapeutic drug target for post-COVID-19 complications
T2 - Life Sciences
AU - Ashraf, Mohammad Saquib
AU - Tuli, Kanika
AU - Moiz, Shadman
AU - Sharma, Satish Kumar
AU - Sharma, Sushila
AU - Sharma, Deepa
AU - Adnan, Mohd
PY - 2024
DA - 2024/12/01
PB - Elsevier
SP - 123202
VL - 359
PMID - 39489398
SN - 0024-3205
SN - 1879-0631
ER -
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BibTex (up to 50 authors)
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@article{2024_Ashraf,
author = {Mohammad Saquib Ashraf and Kanika Tuli and Shadman Moiz and Satish Kumar Sharma and Sushila Sharma and Deepa Sharma and Mohd Adnan},
title = {AMP kinase: A promising therapeutic drug target for post-COVID-19 complications},
journal = {Life Sciences},
year = {2024},
volume = {359},
publisher = {Elsevier},
month = {dec},
url = {https://linkinghub.elsevier.com/retrieve/pii/S0024320524007926},
pages = {123202},
doi = {10.1016/j.lfs.2024.123202}
}
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