http://jcps.bjmu.edu.cn

Journal of Chinese Pharmaceutical Sciences ›› 2022, Vol. 31 ›› Issue (5): 360-368.DOI: 10.5246/jcps.2022.05.031

• Original articles • Previous Articles     Next Articles

Fluvastatin protects against puromycin aminonucleoside-induced podocyte injury by inhibiting TRPC6

Hui Gao1, Yunjing Zhang2, Jing Lin3, Xifeng Sun2,*()   

  1. 1 Department of Urology, Zibo Central Hospital, Zibo 255036, China
    2 Department of Nephrology, Zibo Central Hospital, Zibo 255036, China
    3 Department of Cardiology, Shaanxi Provincial People’s Hospital, Xian 710068, China
  • Received:2021-11-12 Revised:2021-11-30 Accepted:2021-12-21 Online:2022-06-02 Published:2022-06-02
  • Contact: Xifeng Sun

Abstract:

In the present study, we aimed to investigate the effect of puromycin aminonucleoside (PAN) on the expression and distribution of transient receptor potential canonical 6 (TRPC6) of murine podocytes and further study the protective mechanism of fluvastatin on podocyte injury by TRPC6 in vitro. Podocytes were treated by PAN at different doses and at different time points. The expressions of TRPC6 at mRNA and protein levels were assessed. An immunofluorescent assay was used to observe the distribution of TRPC6. Cultured podocytes were then divided into four groups. The expressions of TRPC6 at mRNA and protein levels were measured. The intracellular calcium concentration of podocytes was measured with a laser-scanning confocal microscope. The paracellular permeability to BSA was evaluated using Millicell-PCF Inserts. The expressions of TRPC6 at mRNA and protein levels were increased in a dose and time-dependent manner after exposure to PAN. Immunofluorescence showed that the expression intensity of TRPC6 was significantly increased, and the distribution of TRPC6 was changed after PAN was applied to podocytes. With fluvastatin intervention, PAN-induced up-regulation of TRPC6 was significantly reversed. The ratio of the peak value of intracellular calcium to the basic calcium value in the PAN group was significantly higher after TRPC6 was activated by OAG, while it is obviously reversed under the action of fluvastatin. The podocyte permeability was significantly increased after 48 h of PAN treatment, while the above situation was effectively improved after fluvastatin intervention. The changes of distribution and expression of TRPC6 were related to podocyte injury induced by PAN. Fluvastatin could exert its protective effects on podocytes by down-regulating TRPC6.

Key words: TRPC6, Podocyte, Puromycin aminonucleoside, Fluvastatin, Calcium

Supporting: