Aliskiren prevents hypertension and reduces asymmetric dimethylarginine in young spontaneously hypertensive rats

作者：Tain You Lin^*; Hsu Chien Ning; Lin Ching Yuang; Huang Li Tung; Lau Ying Tung

来源：European Journal of Pharmacology, 2011, 670(2-3): 561-565.

DOI：10.1016/j.ejphar.2011.09.005

• Asymmetric dimethylarginine
• Nitric oxide
• Hypertension

Asymmetric dimethylarginine (ADMA), an endogenous inhibitor of NOS, decreases NO synthesis. Plasma ADMA concentrations increase markedly in hypertension. We tested whether the development of hypertension and the increases in ADMA in spontaneously hypertensive rats (SHR) are prevented by aliskiren, a renin inhibitor. Male SHRs and normotensive Wistar Kyoto (WKY) control rats, aged 4 weeks (pre-hypertensive stage), were assigned to 4 groups: untreated SHRs and WKY rats, and SHRs that received oral aliskiren 10 and 30 mg/kg/day for 6 weeks. All rats were sacrificed at age 10 weeks. Blood pressure decreased at age 6, 8, and 10 weeks in SHRs that received high-dose aliskiren. Aliskiren mitigated the increases in plasma ADMA in SHRs. Renal ADMA levels were lower in SHRs that received high-dose aliskiren versus SHRs. SHRs experienced decreased plasma and kidney L-Arg-to-ADMA ratios versus control rats, which were reverted by 30 mg/kg aliskiren. Renal cortical neuronal NOS-alpha and -beta levels increased in SHRs fed with high-dose aliskiren. Early aliskiren treatment mitigates increases in ADMA, restores L-Arg-to-ADMA ratios, enhances neuronal NOS-alpha, prevents decreased nNOS-beta levels in the kidney which might restore NO bioavailability and contribute to the decrease of blood pressure in young SHRs. Our findings suggest that aliskiren is a therapeutic agent for prehypertension that regulates the ADMA/NO pathway.

• 出版日期2011-11-30
• 单位长春大学; 中国医科大学