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抗高血压治疗对大鼠主动脉结构、力学和代谢特性的影响。

The effects of anti-hypertensive therapy on the structural, mechanical and metabolic properties of the rat aorta.

作者信息

Clark J F, Radda G K, Boehm E A

机构信息

Department of Biochemistry, University of Oxford, UK.

出版信息

J Muscle Res Cell Motil. 2000 Apr;21(3):255-67. doi: 10.1023/a:1005646614308.

DOI:10.1023/a:1005646614308
PMID:10952173
Abstract

The vascular system exhibits altered growth, calcium responses and metabolism during hypertension. To relate such changes, we compared histological, tension and metabolic responses in the aorta from 32-week-old spontaneously hypertensive rats (SHRs), normotensive Wistar-Kyoto (WKY) rats, and SHRs treated with Verapamil (V) and ACE-inhibitor, Trandolapril (T) as well as a combination of the two treatments (C). Vascular hypertrophy was apparent in the SHRs. Contractile responses induced by 50 mmol/1 KCl and 2.5 mmol/1 Ca2+ were significantly lower in the SHR (64.4 mN/mm2 vs. 49.2 mN/mm2), but an associated increase in Ca2+ -sensitivity (EC50 of extracellular Ca2+ (mumol/1): SHR, 456 vs. WKY, 616) normalised tension generating ability. All treatments led to significant decreases in blood pressure, although only T and C treated animals became normotensive with concomitant normalisation of vascular hypertrophy. An increase in oxygen consumption was apparent in the SHR aorta, which was associated with significant differences in the activities of key metabolic enzymes. Anti-hypertensive treatment normalised many of the metabolic parameters, with the C therapy being the most efficacious. We conclude that the treatment of hypertension by combined therapy leads to a better normalisation of structural, contractile, and metabolic parameters in the SHR, than either treatment alone and that metabolic changes with the pathology are resolved with appropriate therapy.

摘要

在高血压期间,血管系统呈现出生长、钙反应和代谢的改变。为了关联这些变化,我们比较了32周龄自发性高血压大鼠(SHR)、血压正常的Wistar-Kyoto(WKY)大鼠以及用维拉帕米(V)和血管紧张素转换酶抑制剂群多普利(T)治疗的SHR,还有两种治疗联合使用(C)时主动脉的组织学、张力和代谢反应。SHR中血管肥大明显。50 mmol/L KCl和2.5 mmol/L Ca2+诱导的收缩反应在SHR中显著降低(64.4 mN/mm2对49.2 mN/mm2),但伴随的Ca2+敏感性增加(细胞外Ca2+的EC50(μmol/L):SHR为456,WKY为616)使张力产生能力正常化。所有治疗均导致血压显著降低,尽管只有T和C治疗的动物血压恢复正常,同时血管肥大也恢复正常。SHR主动脉中氧消耗增加明显,这与关键代谢酶活性的显著差异有关。抗高血压治疗使许多代谢参数恢复正常,联合治疗(C疗法)最为有效。我们得出结论,联合治疗高血压比单独任何一种治疗能使SHR的结构、收缩和代谢参数更好地恢复正常,并且病理状态下的代谢变化可通过适当治疗得到解决。

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