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内皮素对麻醉大鼠动脉压力感受器反射的调制作用

MODULATORY EFFECTS OF ENDOTHELIN ON CAROTID BAROREFLEX IN ANESTHETIZED RATS

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【作者】 李德培范振中何瑞荣

【Author】 LI DE-PEI;FAN ZHEN-ZHONC;HE RUI-RONG (Department of Physiology, Institute of Basic Medicine, Hebei Medical University, Shijiazhuang 050017)

【机构】 河北医科大学基础医学研究所生理室!石家庄050017

【摘要】 在27只隔离灌流颈动脉窦区的麻醉大鼠,观察了内皮素(ET-1)对动脉压力感受器反射的调制作用。结果如下:(1)在颈动脉窦区灌流1nmol/L的ET-1时,压力感受器机能曲线向左下方移位,曲线的最大斜率(PS)由0.40±0.02增至0.51±0.02kPa/kPa(P<0.01),压力感受器反射性血压下降幅度(RD)由5.66±0.23增至6.76±0.22kPa(P<0.01)。由此提示,这一剂量的FT-1对压力感受器反射有易化作用。(2)用10nmol/L的ET-1灌流时,压力感受器机能曲线则向右上方移位,PS降至0.28±0.01kPa/kPa(P<0.01),RD降至4.16±0.19kPa(P<0.01);100nmol/L的ET-1可使压力感受器机能曲线向右上方移位更为明显,PS降至0.19±0.03kPa(P<0.001),RD进一步降至3.33±0.38kPa(P<0.001)。这些结果表明,上述两种剂量的ET-1对压力感受器反射有抑制作用。(3)ETA受体选择性阻断剂BQ123(0.15μmol/L)可以阻断ET-1(10nmol/L)对压力感受器反射的抑制效应。(4)预先灌流KATP通道阻断剂格列苯脲(10μmol/L),也可阻断ET-1的效应。综上所述,ET-1对压力感受器反射有双重效应,低剂量时有易化作用,而较高剂量时则有抑制作用,后一作用由ET-1型受体介导并有KATP通道的参与。

【Abstract】 Modulatory effects of endothelin (ET) on carotid harorellex were examined in 27 anesthetized rats With isolated carotid sinus perfusion. The results obtained were as follows: (1) By perfusing with 1 nmol/L ET-1, the functional curve of carotid baroreflex (FCCB) was shifted to the left and downward with an increase in its peak slope (PS)from 0.40±0.02 to 0.51±0.02 kPa/kPa (P<0.01), while the reflex decrease of mean arterial pressure (RD) was increased from 5. 66±0. 23 to 6.76±0.22 kPa (P<0.01). The above results indicated that this dose of ET-1 facilitated the carotid baroreflex. (2) On the contrary, by perfusing with 10 nmol/L of ET-1, FCCB was shifted to the right and upward with a dearease of PS to 0.28±0.01 kPa/kPa (P<0.01), while RD was decreased to 4. 16±0. 19 kPa (P<0.01). In response to perfusion with 100 nmol/L ET-1,FCCB was further shifted to the right and upward with a marked decrease of PS to 0.19±0.03 kPa/kPa(P<0.001), and RD was conspicuously decreased to 3.33±0.38 kPa (P< 0.001). These results showed that ET-1 at the doses of 10 or 100 nmol/L exerted an inhibitoly action on baroreflex. (3)Selective ETA receptor blocker BQ123 (0.15 μmol/L) might abolish the effects of ET-1 (10 nmol/L) on baroreflex. (4) Prepefusing with KATP channel antagonist glibenclamide (10 μmol/L) could also eliminated the effects of ET-1. Taken together, it is suggested that ET-1 exerts a dual effects on baroreflex, being facilitatory at lower dose and inhibitory at higher dose. The latter effect is mediated by ETA receptor, in which KATP channels may be involved.

  • 【文献出处】 生理学报 ,ACTA PHYSIOLOGICA SINICA , 编辑部邮箱 ,1998年02期
  • 【分类号】Q463
  • 【被引频次】8
  • 【下载频次】28
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