FANG Zhu-yuan, DING Kang, SHEN Zhu-yang, et al. Effects of Qianyang Yuyin Granules on Oxidative Stress and Inflammation Factors in Kidney of Spontaneously Hypertensive Rats[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(13): 86-91.
FANG Zhu-yuan, DING Kang, SHEN Zhu-yang, et al. Effects of Qianyang Yuyin Granules on Oxidative Stress and Inflammation Factors in Kidney of Spontaneously Hypertensive Rats[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(13): 86-91. DOI: 10.13422/j.cnki.syfjx.2016130086.
Objective: To investigate the effects of Qianyang Yuyin granules (QYYYG) on oxidative stress and inflammation factors in kidney of spontaneously hypertensive rats (SHRs). Method: SHRs were randomly divided into model group
QYYYG group
Benazepril group
and QYYYG+Benazepril group. The rats received QYYYG suspension (5 g·kg-1)
Benazepril suspension (1.67 mg·kg-1)
QYYYG suspension (5 g·kg-1)+Benazepril suspension (1.67 mg·kg-1) respectively by intragastric administration. WKY rats were used as normal group
and their renal tissues were collected after 8 weeks of same volume administration.The changes of blood pressure
trace albumin
and creatinine in rats were observed;local NADPH oxidase-4 (NOX4) levels
nuclear factor-κB (NF-κB) p65
interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) protein expression levels of kidney were detected by Western blot;the effects of QYYYG on the release of these indicators were observed. Result: Compared with the normal group
the model gorup showed significant increase in blood pressure
trace albumin
and creatinine in rats
and NOX4
NF-κB p65
IL-6
and TNF-α protein expression levels in kidney of SHRs(P < 0.01). QYYYG can inhibit the expression of NOX4
reduce the NF-κB p65
IL-6
and TNF-α protein expression levels in kidney of SHRs
meanwhile it can reduce blood pressure
trace ablumin
and creatintine(P < 0.01)
and the synergy effect was more obvious in case of combination of Qianyang Yuyin granules and Benazepril. Conclusion: QYYYG can improve the renal impairment of SHRs
and the mechanism may be associated with inhibiting oxidative stress and reducing the release of inflammation factors.