Clozel M, Watanabe H
Pharma Division, Preclinical Research, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Life Sci. 1993;52(9):825-34. doi: 10.1016/0024-3205(93)90081-d.
The aim of this study was to evaluate the role of endothelin and endothelin ETA receptor in the early cerebral vasoconstriction following subarachnoid hemorrhage (SAH) in the rat. SAH induced by injection of autologous blood in the cisterna magna reduced by 22 to 38% cerebral blood flow (CBF) measured with radioactive microspheres at 30, 60 and 120 min after SAH. The cyclic pentapeptide BQ-123, a selective antagonist of the ETA receptor, injected intravenously (3 mg/kg) had no effect on this decrease in CBF. However, intracisternal BQ-123 (10 nmol) completely prevented the decrease in CBF at 60 and 120 min after SAH. These results suggest that BQ-123 does not cross the blood-brain barrier, but demonstrate that endothelin acting on ETA receptor plays a role in the pathogenesis of cerebral vasoconstriction in this rat model of SAH.
本研究的目的是评估内皮素和内皮素ETA受体在大鼠蛛网膜下腔出血(SAH)后早期脑血管收缩中的作用。通过在大鼠枕大池注射自体血诱导SAH,在SAH后30、60和120分钟用放射性微球测量,脑血流量(CBF)减少了22%至38%。静脉注射(3mg/kg)选择性ETA受体拮抗剂环五肽BQ-123对CBF的这种减少没有影响。然而,脑池内注射BQ-123(10nmol)完全阻止了SAH后60和120分钟时CBF的减少。这些结果表明BQ-123不能穿过血脑屏障,但表明作用于ETA受体的内皮素在该SAH大鼠模型的脑血管收缩发病机制中起作用。