Burke T J, Falk S, Conger J D, Voelkel N F
Division of Renal Diseases and Hypertension, University of Colorado Medical School, Denver 80262, USA.
Ren Fail. 1999 Jan;21(1):23-33. doi: 10.3109/08860229909066967.
The present studies measured vessel diameter, before and after addition of hemolysate, in isolated afferent arterioles (AA) and efferent arterioles (EA) obtained from the rat kidney. Human red blood cells (RBC) were hemolyzed in distilled water and membranes were discarded after centrifugation. Hemolysate added to the bath solution caused vigorous AA and EA contraction and, after washout, hypersensitized the AA and EA to doses of angiotensin II (AII) which would normally only elicit 50% contraction (EC50). Neither the contraction nor the hypersensitization were mimicked by pure human hemoglobin. The vasoconstrictive responses in the AA and EA were accompanied by increased cytosolic-free calcium concentration. Further purification (desalting) of the hemolysate to remove substance of < or = 1000 Da (which include ATP) did not eliminate the vasoconstrictive component from the hemolysate. Finally, cultured rat aortic vascular smooth muscle cells also demonstrated a rapid increase in (Ca2+i) when exposed to hemolysate. This increase in (Ca2+i) was, in part, dependent on Ca2+ influx since it could be attenuated with diltiazem (10(-5) M). In conclusion, hemolysate contains a factor which induces contractions of the isolated rat kidney AA and EA and rapid elevations in (Ca2+i). This factor, from hemolyzed RBC, is not hemoglobin itself.
本研究测量了从大鼠肾脏获取的离体入球小动脉(AA)和出球小动脉(EA)在添加溶血产物前后的血管直径。人红细胞(RBC)在蒸馏水中溶血,离心后弃去细胞膜。向浴液中添加溶血产物会引起AA和EA剧烈收缩,洗脱后,AA和EA对通常仅引起50%收缩(EC50)剂量的血管紧张素II(AII)变得超敏。纯人血红蛋白既不能模拟收缩反应也不能模拟超敏反应。AA和EA中的血管收缩反应伴随着胞质游离钙浓度的增加。对溶血产物进行进一步纯化(脱盐)以去除分子量小于或等于1000 Da的物质(包括ATP)并不能消除溶血产物中的血管收缩成分。最后,培养的大鼠主动脉血管平滑肌细胞在暴露于溶血产物时也表现出(Ca2 + i)的快速增加。这种(Ca2 + i)的增加部分依赖于Ca2 +内流,因为它可以被地尔硫卓(10^(-5) M)减弱。总之,溶血产物含有一种能诱导离体大鼠肾脏AA和EA收缩以及(Ca2 + i)快速升高的因子。这种来自溶血红细胞的因子不是血红蛋白本身。