The effect of valsartan on renin-angiotensin system of chronic hepatitis and liver cirrhosis
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摘要: 研究缬沙坦对慢肝、肝硬化患者肾素 -血管紧张素系统 (RAS)的影响并探讨其作用机制。 5 4例慢肝、肝硬化患者 ,随机分为治疗组和对照组。对照组给予常规保肝治疗 ,治疗组在常规治疗的基础上加用缬沙坦 80mg/日 ,疗程 1个月。采用放免法检测治疗前后血清肾素 (PRA)、血管紧张素Ⅱ (AⅡ )、醛固酮 (ALD)的变化 ;采用半定量逆转录PCR技术测定治疗组 5例慢肝患者缬沙坦治疗前后血管紧张素原mRNA、血管紧张素ⅡⅠ型受体mRNA表达的变化。结果发现经缬沙坦治疗后 ,血清PRA、AⅡ均较治疗前明显升高 ,ALD则明显降低。与对照组相比 ,治疗组治疗后血清RAS各激素水平的变化均有显著性差异 ,而肝组织血管紧张素原mRNA、血管紧张素ⅡⅠ型受体mRNA的表达较治疗前降低。研究提示缬沙坦可以有效抑制慢性肝病患者循环和肝组织局部RAS的过度激活 ,对慢肝、肝硬化患者的治疗有一定的积极作用
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关键词:
- 缬沙坦 /
- 慢性肝病 /
- 肾素-血管紧张素系统
Abstract: To study the effect of valsartan on renin-angiotensin system (RAS) of chronic hepatitis and liver cirrhosis 54chronic hepatitis and liver cirrhosis patients were randomly divided into two groups: therapy group and control group. 27 cases in each group. The control group was treated with routine treatment, the therapy group, besides routine treatment, was added valsartan 80mg/day. The therapy period is 1 month. Before and after treatment, serum renin (PRA) ?angiotensin Ⅱ (AⅡ) ?aldosterone (ALD) were measured by radioimmunoassay. In therapy group, before and after therapy, 5 cases of chronic hepatitis patients' liver tissue were obtained by liver biopsy, then semi-quantity RT-PCR method was used to measure the expression of liver tissue angiotensinogen mRNA?angiotensin Ⅱ type Ⅰ receptor mRNA. As a result, in therapy group, after treated with valsartan, the PRA?AⅡ were elevated remarkably (P<0.05) , ALD was lower (P<0.05) ?In therapy group, the patients' PRA?AⅡ were all elevate significantly (P<0.01) , the ALD was decreased (P<0.001) ;after treated by valsartan, the expression of liver tissue angiotensinogen mRNA?angiotensin Ⅱ type Ⅰ receptor mRNA were all lower than before (P<0.05) . So valsartan can modulate the patients' circulation and local liver tissue renin-angiotensin system, thus inhibit the overactive of the renin-angiotensin-aldosterone system in patients with chronic hepatitis and liver cirrhosis.-
Key words:
- valsartan /
- chronic hepatitis /
- liver cirrhosis
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[1] 病毒性肝炎防治方案[J].中华肝脏病杂志, 2000, 6∶324-329. [2]MartinPaul, JurgenWagner, VictorJ , etal.Geneexpressionoftherenin-angiotensinsysteminhumantissues:quantitativeanalysisbythepolymerasechainreaction[J].JClinInvest, 1993, 91∶2058-2064. [3]TerryMorgan, CatherineCraven, LennethWard, etal.Humanspiralarteryreninangiotensinsystem[J].Hypertation, 1998, 32∶683-687. [4]Goodfriendt, EliottM , CattK .etal.AngiotensinⅡreceptorandtheirantagonist[J].NEnglJMed, 1996, 334∶1649-1654. [5]HiroshiIwao, AkioNakamara, KiyoshiFuhui, etal.Endogenousan giotensinⅡregulateshepaticangiotensinogenproduction[J].Lifesci ence, 1990, 47∶2343-2349. [6] 卢建, 余应年, 徐仁宝.受体信号转导系统与疾病[M].济南:山东科学技术出版社, 2001.628-630. [7]张晶, 魏红山, 李定国.血管紧张素Ⅱ与肝硬化[J].中华消化杂志, 2002, 22 (6) ∶363-365.
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