Yokoyama S, Benoit J N
Department of Physiology and Biophysics, Louisiana State University Medical Center, Shreveport 71130, USA.
Am J Physiol. 1996 May;270(5 Pt 1):G752-6. doi: 10.1152/ajpgi.1996.270.5.G752.
The effects of bradykinin on lymphatic pump activity of rat mesenteric collecting duct were studied, and the receptor subtype responsible for the bradykinin response was evaluated. Rats were anesthetized with intraperitoneal alpha-chloralose and urethan, and exteriorized mesenteries were studied using intravital microscopic techniques. The diameter of the collecting lymph vessels (approximately 100 microns) was continuously monitored and lymphatic pump parameters (end diastolic diameter, end systolic diameter, stroke volume index, ejection fraction, contraction frequency, and pump flow index) were calculated. Bradykinin (0.1-1.0 nM) did not affect end diastolic diameter, end systolic diameter, stroke volume index, and ejection fraction. Bradykinin increased lymphatic contraction frequency and pump flow index in a dose-dependent manner. Des-Arg9-[Leu8]bradykinin (B1 antagonist, 0.1 microM) had no effect on baseline lymphatic pumping but completely inhibited the bradykinin-induced increase in contraction frequency. N-acetyl-D-Arg-[Hyp3,Thi5,8,D-Phe7] bradykinin (B2 antagonist, 0.1 microM) significantly depressed lymphatic contraction frequency in baseline conditions but had no effect on bradykinin-induced increases in contraction frequency. These results indicate that bradykinin induces positive chronotropic but not inotropic effects on lymphatic pump activity through the stimulation of B1 receptors.
研究了缓激肽对大鼠肠系膜集合淋巴管淋巴泵活动的影响,并评估了介导缓激肽反应的受体亚型。用腹腔注射α-氯醛糖和乌拉坦麻醉大鼠,采用活体显微镜技术研究暴露的肠系膜。连续监测集合淋巴管(约100微米)的直径,并计算淋巴泵参数(舒张末期直径、收缩末期直径、每搏量指数、射血分数、收缩频率和泵流量指数)。缓激肽(0.1 - 1.0 nM)不影响舒张末期直径、收缩末期直径、每搏量指数和射血分数。缓激肽以剂量依赖的方式增加淋巴收缩频率和泵流量指数。去精氨酸9 - [亮氨酸8]缓激肽(B1拮抗剂,0.1 microM)对基线淋巴泵活动无影响,但完全抑制缓激肽诱导的收缩频率增加。N - 乙酰 - D - 精氨酸 - [Hyp3,Thi5,8,D - 苯丙氨酸7]缓激肽(B2拮抗剂,0.1 microM)在基线条件下显著降低淋巴收缩频率,但对缓激肽诱导的收缩频率增加无影响。这些结果表明,缓激肽通过刺激B1受体对淋巴泵活动产生正性变时作用而非变力作用。