Hemolysate-mediated renal vasoconstriction and hypersensitization

被引:5
作者
Burke, TJ [1 ]
Falk, S [1 ]
Conger, JD [1 ]
Voelkel, NF [1 ]
机构
[1] Univ Colorado, Sch Med, Div Renal Dis & Hypertens, Denver, CO 80262 USA
关键词
kidney; afferent arteriole; efferent arteriole; VSMC; renal vascular resistance; fluorescence; fura-2;
D O I
10.3109/08860229909066967
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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 cytosotic-free calcium concentration. Further purification (desalting) of the hemolysate to remove substances of less than or equal to 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 (Ca(2+)i) when exposed to hemolysate. This increase in (Ca(2+)i) was, in part, dependent on Ca2+ influx since if 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 (Ca(2+)i). This factor, from hemolyzed RBC, is not hemoglobin itself.
引用
收藏
页码:23 / 33
页数:11
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