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人体内的P物质与原发性高血压

Substance P in human essential hypertension.

作者信息

Faulhaber H D, Oehme P, Baumann R, Enderlein J, Rathsack R, Rostock G, Naumann E

机构信息

Central Institute for Cardiovascular Research, Academy of Sciences of the G.D.R., Berlin.

出版信息

J Cardiovasc Pharmacol. 1987;10 Suppl 12:S172-6.

PMID:2455174
Abstract

Substance P (SP) plays an important role in central nervous and peripheral blood pressure regulation. Its effects include modulating influence on the adrenergic system and inhibition of stress-induced plasma noradrenaline increase in animal studies. In patients with essential hypertension (n = 45, WHO stages 1 and 2) the SP-like immunoreactivity (SPLIR) was found significantly (p less than 0.01) lower (1.36 +/- 0.23 pg/100 microliters) than in 24 normotensive subjects (4.54 +/- 0.72 pg/100 microliters). Furthermore, the influence of a mental stress test on SPLIR was investigated in patients with essential hypertension (n = 11, WHO stage 1) and compared with nine normotensive subjects. Whereas in normotensive subjects plasma SP increased under a standardized mental arithmetic test (4.03 +/- 0.48 to 4.74 +/- 0.56 pg/100 microliters), in hypertensive patients a decrease of SP from lower baseline levels (2.85 +/- 0.54 to 2.57 +/- 0.54 pg/100 microliters) was demonstrated. The significantly different changes of plasma SP in normotensive and hypertensive subjects under mental stress conditions had the opposite direction in comparison with the adrenergic reaction [higher and prolonged increase of plasma noradrenaline (NA) in the hypertensive group]. Under antihypertensive drug treatment with prazosin (4.5 mg/day, n = 10) or with captopril (450 mg/day, n = 10) an increase of plasma SP was registered. The results support the participation of SP in the pathogenesis of human hypertension and in therapeutic mechanisms. Lower plasma levels and decreased responsiveness of SP possibly represent the enhanced stress sensitivity in primary hypertension.

摘要

P物质(SP)在中枢神经系统和外周血压调节中发挥重要作用。在动物研究中,其作用包括对肾上腺素能系统的调节影响以及抑制应激诱导的血浆去甲肾上腺素升高。在45例原发性高血压患者(WHO 1期和2期)中,发现SP样免疫反应性(SPLIR)显著(p<0.01)低于24例血压正常受试者(4.54±0.72 pg/100微升)(1.36±0.23 pg/100微升)。此外,对11例原发性高血压患者(WHO 1期)进行了心理应激试验对SPLIR的影响研究,并与9例血压正常受试者进行了比较。在血压正常受试者中,在标准化心算试验下血浆SP升高(4.03±0.48至4.74±0.56 pg/100微升),而在高血压患者中,SP从较低的基线水平下降(2.85±0.54至2.57±0.54 pg/100微升)。与肾上腺素能反应相比,血压正常和高血压受试者在心理应激条件下血浆SP的显著不同变化方向相反[高血压组血浆去甲肾上腺素(NA)升高且持续时间更长]。在用哌唑嗪(4.5 mg/天,n = 10)或卡托普利(450 mg/天,n = 10)进行抗高血压药物治疗后,血浆SP有所升高。这些结果支持SP参与人类高血压的发病机制和治疗机制。血浆SP水平降低和反应性降低可能代表原发性高血压中应激敏感性增强。

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