Abstract

Objective To investigate the effect of RhoA inhibitor Y27632 on the apoptosis of hippocampal neurons in neonatal rats induced by propofol. Methods Forty-eight neonatal Sprague Dawley (SD) rats at postnatal day 7 (P7) were randomly divided into normal saline group (NS group), RhoA inhibitor group (Y27632 group), Propofol group (Pro group) and RhoA inhibitor+ Propofol group (Y27632+ Pro group). NS group and Pro group were administrated intraperitoneally with 150μl normal saline.Twenty minutes later, Y27632 group and Y27632+ Pro group were administrated intraperitoneally with 1 mg·kg-1 Y27632.And then the Pro group and Y27632+ Pro group were exposed to propofol with first administration 30 mg·kg-1 and repeated administration 15 mg·kg-1for five times once an hour.Twenty-four hours after the final dose of the propofol, TUNEL was used to detect neuronal apoptosis of the hippocampal cells (n=6). And then, Western blot was used to test the proteins expression of cleaved caspase-3, calpainⅡ, Bcl-2 and Bax (n=6). Results (1) The number of TUNEL positive cells in the hippocampal CA1 region were increased by 208.7% in Pro group ((84.10±12.03)/mm2) compared with that in NS group((27.24±6.29)/mm2) (P 0.05). Conclusion RhoA inhibitor Y27632 can alleviate the hippocampus neuronal apoptosis of neonatal rat induced by propofol. Key words: Propofol; RhoA inhibitor; Hippocampus; Apoptosis

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