Transient receptor potential channel 1/4 (TRPC1/4) are considered to be related to subarachnoid hemorrhage (SAH)-induced cerebral vasospasm. In this study， a SAH rat model was employed to study the roles of TRPC1/4 in the early brain injury (EBI) after SAH. Primary cultured hippocampal neurons were exposed to oxyhemoglobin to mimic SAH in vitro. The protein levels of TRPC1/4 increased and peaked at 5 days after SAH in rats. Inhibition of TRPC1/4 by SKF96365 aggravated SAH-induced EBI， such as cortical cell death (by TUNEL staining) and degenerating (by FJB staining). In addition， TRPC1/4 overexpression could increase calcineurin activity， while increased calcineurin activity could promote the dephosphorylation of N-methyl-D-aspartate receptor (NMDAR). Calcineurin antagonist FK506 could weaken the neuroprotection and the dephosphorylation of NMDAR induced by TRPC1/4 overexpression. Contrarily， calcineurin agonist chlorogenic acid inhibited SAH-induced EBI， even when siRNA intervention of TRPC1/4 was performed. Moreover， calcineurin also could lead to the nuclear transfer of nuclear factor of activated T cells (NFAT)， which is a transcription factor promoting the expressions of TRPC1/4. TRPC1/4 could inhibit SAH-induced EBI by supressing the phosphorylation of NMDAR via calcineurin. TRPC1/4-induced calcineurin activation also could promote the nuclear transfer of NFAT， suggesting a positive feedback regulation of TRPC1/4 expressions.