Wright G L, Huang B S, Johnson P J, McCumbee W D
Department of Physiology, Marshall University School of Medicine, Huntington, WV 25704-2901.
Can J Physiol Pharmacol. 1988 Oct;66(10):1278-81. doi: 10.1139/y88-209.
It was recently shown that a peptide (hypertensive factor, HF) isolated from erythrocyte hemolysates from spontaneously hypertensive rats induced a prolonged elevation of blood pressure in normotensive rats. In addition, the peptide produced a marked stimulation of the in vitro uptake of lanthanum-resistant calcium by the aortae and enhanced the contractile response of aortic rings to constrictor agents. The present report describes findings of calcium stimulatory activity, enhancement of contractile function, or pressor activity in extracts of homogenates from several tissues of the rat and from erythrocyte hemolysates of several mammalian species. Significant stimulation of calcium uptake in aortic rings was obtained with preparations from rat brain, liver, and kidney. The activity per weight of tissue was similar for brain and kidney (approximately 2 units/g), while liver exhibited somewhat higher concentrations (4 units/g). The diffusate of cardiac tissue did not significantly alter in vitro calcium uptake by aortae. The injection of the cardiac and liver diffusates into normotensive Wistar-Kyoto rats produced slight (10 Torr) (1 Torr = 133.3Pa) and moderate (25 Torr) elevations of blood pressure, respectively. Finally, a peptide purified from homogenates of rat brain by the protocol developed for the purification of HF from erythrocytes was shown to significantly enhance the contractile response of aortic rings to K+ and norepinephrine. Diffusates of erythrocytes from the rat, rabbit, dog, and guinea pig each caused a significant stimulation of calcium uptake and contained approximately the same level of activity (500 units/L of whole blood). Diffusates prepared from outdated human erythrocytes had no significant effect on calcium uptake, whereas those of freshly drawn samples exhibited high levels of activity.(ABSTRACT TRUNCATED AT 250 WORDS)
最近研究表明,从自发性高血压大鼠的红细胞溶血产物中分离出的一种肽(高血压因子,HF)可使正常血压大鼠的血压长时间升高。此外,该肽能显著刺激主动脉对镧抗性钙的体外摄取,并增强主动脉环对收缩剂的收缩反应。本报告描述了大鼠几种组织匀浆提取物以及几种哺乳动物红细胞溶血产物中钙刺激活性、收缩功能增强或升压活性的研究结果。用大鼠脑、肝和肾的提取物可使主动脉环的钙摄取得到显著刺激。脑和肾每克组织的活性相似(约2单位/克),而肝的浓度略高(4单位/克)。心脏组织的扩散液对主动脉的体外钙摄取没有显著影响。将心脏和肝脏的扩散液分别注射到正常血压的Wistar - Kyoto大鼠体内,可使血压分别轻度升高(10 Torr)(1 Torr = 133.3Pa)和中度升高(25 Torr)。最后,按照从红细胞中纯化HF的方案从大鼠脑匀浆中纯化出的一种肽,可显著增强主动脉环对钾离子和去甲肾上腺素的收缩反应。大鼠、兔、狗和豚鼠的红细胞扩散液均能显著刺激钙摄取,且活性水平大致相同(500单位/升全血)。陈旧人红细胞制备的扩散液对钙摄取无显著影响,而新鲜采集样本的扩散液则表现出高活性。(摘要截短于250字)