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作 者:徐春[1] 孙明智[1] 李玉荣[1] 杨宝峰[1]
机构地区:[1]哈尔滨医科大学生理学教研室,哈尔滨医科大学药理学教研室
出 处:《中国应用生理学杂志》1995年第3期244-246,共3页Chinese Journal of Applied Physiology
摘 要:用荧光染色法观察了合成的大鼠降钙素基因相关肽(CGRP)对大鼠心肌细胞内游离Ca ̄(2+)含量的影响。结果证明,CGRP能明显增加心肌细胞内Ca ̄(2+)含量,小、中和大剂量(10 ̄(-9)、10 ̄(-8)、10 ̄(-7)mol/L)的CGRP使Ca ̄(2+)含量分别增加至276.88±6.31、364.997±12.70、576.397±15nmol/L与对照组(136.28±7.24nmol/L)相比差异非常显著(P<0.01),且随着CGRP剂量的增加而作用明显加强,呈现剂量—效应关系。30μmol/L的维拉帕米对CGRP所致的细胞内Ca ̄(2+)增加有抑制作用,对小、中、大剂量CGRP作用的抑制率分别为48%、44%和18%。我们推测,CGRP可能直接作用于心肌细胞。低浓度CGRP的正性肌力作用主要是促进Ca ̄(2+)经Ca ̄(2+)通道内流,使心肌细胞内Ca ̄(2+)含量增加的结果。在大剂量CGRP的正性肌力作用中Ca ̄(2+)内流也起到一定作用。The effect of synthetic rat CGRP on intracellular free Ca ̄(2+) content was observed in the iso-lated rat cardiac myocyte. The results showed that CGRP increased significantly intracellularCa ̄(2+) content from 136.28 ± 7.24nmol/L in the control to 276.88 ± 6.31. 365.00 ± 12.70 and576.40± 15nmol/ L in small(10 ̄(-9) mol/ L),medium(10 ̄(-8)mol/L)and large CGRP dosage(10 ̄(-7)mol / L)groups respectively with a dose─dependent manner. When verapamil(30μmol / L)was given simultaneously with CGRP at the three dosages mentioned above, the increased Ca ̄(2+)content induced by CGRP was depressed.The rates of depression of Ca ̄(2+) at small and mediumdosages of CGRP were 48%, 44% respectively,which were significantly higher than that in largeCGRP dosage (18%).It is,therefore,considered that the positive inotropic action of CGRP atlow concentration is the result of enhancing influx of Ca ̄(2+)into the cell through Ca ̄(2+) channel.The influx of Ca ̄(2+) also plays a certain role in the positive inotropic action of CGRP at highdosage.
分 类 号:R331.31[医药卫生—人体生理学] Q516[医药卫生—基础医学]
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