利钠肽增强诱导实验性高血糖大鼠胍基环化酶活性和血管舒张。

H. Kook, Jongun Lee, S. Kim, Sang Woo Kim, Y. H. Baik
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引用次数: 10

摘要

本研究旨在探讨高血糖是否会改变血管利钠肽受体(NPR)的调节。用链脲佐菌素(50 mg/kg,静脉注射)诱导大鼠高血糖。采用逆转录聚合酶链反应和体外受体放射自显影法测定不同亚型NPR在胸主动脉中的表达。测定了离体胸主动脉对利钠肽反应的等长张力和冠酰环化酶活性。链脲佐菌素治疗后,血浆心房钠素(ANP)浓度显著升高。NPR-A表达增加,NPR-C表达减少。受体结合研究表明,NPR的最大结合能力增加,其亲和力没有明显改变。ANP对大鼠血管舒张程度和冠酰环化酶活性的影响显著增加。另一方面,乙酰胆碱或硝普钠对cGMP的血管舒张反应和组织形成显著降低。这些结果表明,高血糖可能导致血管NPR调节的改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Augmented natriuretic peptide-induced guanylyl cyclase activity and vasodilation in experimental hyperglycemic rats.
The present study was aimed to investigate whether hyperglycemia may alter the regulation of vascular natriuretic peptide receptors (NPR). The hyperglycemia was induced in rats by the treatment with streptozotocin (50 mg/kg, i.v.). The expression of different subtypes of NPR was determined in the thoracic aorta by reverse transcriptase-polymerase chain reaction and quantitative in vitro receptor autoradiography. The isometric tension and the guanylyl cyclase activity of the isolated thoracic aorta in response to natriuretic peptides were also determined. Following the treatment with streptozotocin, the plasma concentration of atrial natriuretic peptide (ANP) was significantly increased. The expression of NPR-A was increased, while that of NPR-C was reduced. The receptor binding study demonstrated an increased maximal binding capacity of NPR, with its affinity not significantly altered. The magnitude of vasodilation and guanylyl cyclase activity in response to ANP was significantly increased. On the other hand, the vasodilator response as well as the tissue formation of cGMP in response to acetylcholine or sodium nitroprusside was significantly reduced. These results indicate that the hyperglycemia may cause an altered regulation of vascular NPR.
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