Numerous studies have demonstrated that endothelin-1 combines with endothelin receptor A,resulting in intense vasoconstriction.Although calcitonin gene-related peptide(CGRP) suppresses endothelin-1,CGRP and endothelin receptor A exhibit direct biological effects on brain tissue.The present study analyzed CGRP and endothelin receptor A expression following subarachnoid hemorrhage in rabbits using immunohistochemistry.CGRP expression was significant at 5 days after model establishment,and endothelin receptor A expression was significant at 3 days after model induction.The perimeter of the basilar artery was measured to determine the amount of cerebral vasospasm.Analytical results revealed a significantly shortened basilar artery perimeter following subarachnoid hemorrhage.Changes in the basilar artery perimeter were negatively associated with endothelin receptor A expression,but positively correlated with CGRP expression in vessels.These results suggest that following subarachnoid hemorrhage,CGRP and endothelin receptor A expressions dynamically changed in brain vessels and tissues,although these changes were not synchronous.Changes in endothelin receptor A expression exhibited a significant effect on the occurrence and development of delayed cerebral vasospasm and delayed neuronal death,while CGRP relaxed vessels and protected nerves. Numerous studies have demonstrated that endothelin-1 combines with endothelin receptor A, resulting in intense vasoconstriction. Although calcitonin gene-related peptide (CGRP) suppresses endothelin-1, CGRP and endothelin receptor A exhibit direct biological effects on brain tissue. CGRP and endothelin receptor A expression following subarachnoid hemorrhage in rabbits using immunohistochemistry. CGRP expression was significant at 5 days after model establishment, and endothelin receptor A expression was significant at 3 days after model induction. The perimeter of the basilar artery was measured to determine the amount of cerebral vasospasm. Analytical results revealed a marked shortened basilar artery perimeter following subarachnoid hemorrhage. Changes in the basilar artery perimeter were negatively associated with endothelin receptor A expression, but positively correlated with CGRP expression in vessels. These results suggest that following subarachnoid hemorrhage hage, CGRP and endothelin receptor A expressions dynamically changed in brain vessels and tissues, although these changes were not synchronous. Change in endothelin receptor A expression exhibited a significant effect on the occurrence and development of delayed cerebral vasospasm and delayed neuronal death, while CGRP relaxed vessels and protected nerves.