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作 者:刘正湘[1,2] 唐家荣[1,2] 任大宏[1,2] 吴翠环[1,2] 陈多恩
机构地区:[1]同济医科大学附属同济医院心内科 [2]同济医科大学病理学教研室
出 处:《中国组织化学与细胞化学杂志》1997年第2期7-11,112,共6页Chinese Journal of Histochemistry and Cytochemistry
基 金:国家自然科学基金
摘 要:本文采用自发性高血压大鼠(SHR)动脉平滑肌细胞培养,3H-胸腺嘧啶核苷(3H-TdR)和3H-亮氨酸(3H-Leucine)掺入方法,观察到用氨氯地平(Amlodipine)作用48小时后,与神经肽Y(NPY)组比较,其离体培养的SHR动脉平滑肌细胞3H-TdR掺入量降低50.5%,3H-Leucine掺入量降低56.5%。氨氯地平组与对照组比较其3H-TdR和3H-Leucine掺入量分别降低57.6%和32.3%。用NPY作用24小时后,与对照组比较动脉平滑肌细胞3H-TdR和3H-Leucine掺入量却分别增加20%和54.6%。而细胞计数均无显著性差异(P>0.05)。结果表明,氨氯地平能有效地抑制SHR血管平滑肌细胞(VSMC)的DNA和蛋白质合成,以及显著的抑制NPY引起的VSMC的DNA合成和蛋白质合成增加效应。Adding 3H Leucine in cultured arterial smooth muscle cells of spontaneously hypertensive rats(SHR), we have compared the Amoldipinlgroup compared with Neuropeptide Y(NPY) group. 48 hours after being given Amlodipine, the mixed amount of 3H TdR in cultured arterial smooth musle cells of SHR reduced to 50 5% and that of 3H Leucine reduced to 56 5%. Compared with the contul group, the mixed amount of 3H TdR and 3H Leucine reduced to 57 6% and 32 3% respectively. 24 hours after being given NPY. the mixed amout of 3H TdR and 3H Leucine increased by 20% and 54 6% respectively. However, the number of arterial smooth muscle cells in three groups had no obvious discrepancy(<0 05). The results showed that Amlodipine could effectively inhibit the increaseing synthesis of DNA and protein caused by NPY in vascular smooth muscle cells of SHR. In suggested that Amlodipin played a considerable role in inhibiting development and advancement of hypertrophy of cardiovascular wall initiated by hypertension.
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