4.7 Article

Sanqi Oral Solution Ameliorates Renal Ischemia/Reperfusion Injury via Reducing Apoptosis and Enhancing Autophagy: Involvement of ERK/mTOR Pathways

Journal

FRONTIERS IN PHARMACOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2020.537147

Keywords

renal ischemia-reperfusion (I; R); acute kidney injury (AKI); Radix Astragali; Radix Notoginseng; apoptosis; autophagy; extracellular signal-regulated kinase (ERK); mammalian target of rapamycin (mTOR)

Funding

  1. Traditional Chinese Medicine Bureau of Guangdong Province [20181133]
  2. National Natural Science Foundation of China [81774216, 81974565]
  3. Specific Research Fund for TCM Science and Technology of Guangdong Provincial Hospital of Chinese Medicine [YN2016QJ12]
  4. Science and Technology Planning Project of Guangdong Province [2018B030322012, 2016A020226042]
  5. Specific Fund of State Key Laboratory of Dampness Syndrome of Chinese Medicine [SZ2020ZZ04]
  6. Medical Scientific Research Foundation of Guangdong Province [A2020323]
  7. Key Project of High-level University Construction of Guangzhou University of Chinese Medicine [XK2019023]

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Ischemia-reperfusion (I/R) induced acute kidney injury (AKI) is a significant health problem with high morbidity and mortality, yet prophylaxis strategies and effective drugs are limited. Sanqi oral solution (SQ) is a formulated medicine widely used in clinical settings to treat various renal diseases via enriching qi and activating blood circulation while its role on I/R-AKI remains unclear. Herein, by establishing rat I/R-AKI models, we intended to investigate the effect of SQ on the prevention of I/R-AKI and explore its underlying mechanisms. We demonstrated that SQ treatment significantly attenuated renal dysfunction of I/R-AKI, alleviated histological damages, inhibited renal apoptosis, and enhanced autophagy. Further investigation proved that SQ could significantly inhibit the activation of ERK and mTOR signaling pathways. Moreover, its renoprotective effect can be abolished by autophagy inhibitor 3-methyladenine (3-MA). Collectively, our results suggest that SQ exerts renoprotective effects on renal I/R injury via reducing apoptosis and enhancing autophagy, which are associated with regulating ERK/mTOR pathways.

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