百日咳毒素增强Gi蛋白表达的失活可减轻自发性高血压大鼠高血压的发展

Yuan Li, M. Anand-Srivastava
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引用次数: 73

摘要

摘要:我们之前的研究表明,自发性高血压大鼠(SHR)在高血压发生之前,Gi蛋白的表达增强可能是高血压发病的因素之一。在本研究中,我们证明,通过腹腔注射百日咳毒素(PT, 1.5 μ g/ 100g体重)使2周龄高血压前期SHR的Gi蛋白失活,可防止高血压发展至4周,此后,高血压开始增加,并在6周后达到未治疗SHR的水平。4周后第二次注射PT可使血压升高延迟一周。通过体外ADP核糖基化和免疫印迹测定,pt诱导的6周龄SHR血压下降与心脏中Gi&agr; 2和Gi&agr; 3蛋白水平下降有关。Gi蛋白水平下降反映在Gi功能下降。此外,在接受pt治疗的SHR中,血压升高到与未接受治疗的SHR相同的水平,与Gi的表达和功能增强有关。这些结果表明,在高血压前期SHR中,通过PT治疗使Gi蛋白失活可以减轻高血压的发展,并提示Gi蛋白水平的升高导致cAMP水平的降低和相关的细胞功能受损可能是SHR中高血压发病的重要因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inactivation of Enhanced Expression of Gi Proteins by Pertussis Toxin Attenuates the Development of High Blood Pressure in Spontaneously Hypertensive Rats
Abstract— We have previously shown that the enhanced expression of Gi proteins in spontaneously hypertensive rats (SHR) that precedes the development of high blood pressure may be one of the contributing factors in the pathogenesis of hypertension. In the present study, we demonstrate that the inactivation of Gi proteins by intraperitoneal injection of pertussis toxin (PT, 1.5 &mgr;g/100 g body wt) into 2-week-old prehypertensive SHR prevented the development of hypertension up to 4 weeks and that, thereafter, it started to increase and reached the same level found in untreated SHR after 6 weeks. A second injection of PT after 4 weeks delayed the increase in blood pressure for another week. The PT-induced decrease in blood pressure in 6-week-old SHR was associated with a decreased level of Gi&agr;-2 and Gi&agr;-3 proteins in the heart, as determined by in vitro ADP ribosylation and immunoblotting. The decreased level of Gi proteins was reflected in decreased Gi functions. Furthermore, an augmentation of blood pressure to the same level in PT-treated SHR as found in untreated SHR was associated with enhanced expression and function of Gi. These results indicate that the inactivation of Gi proteins by PT treatment in prehypertensive SHR attenuates the development of hypertension and suggest that the enhanced levels of Gi proteins that result in the decreased levels of cAMP and associated impaired cellular functions may be contributing factors in the pathogenesis of hypertension in SHR.
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