Corticosterone, a principal glucocorticoid synthesized in the rodent adrenal cortex, can be cumula- tively toxic to hippocampal neurons, the cause of which is not known. The present study determined whether the cytosol adenylate kinase （AK） system long-term exposure to high corticosterone levels. We was involved in the neuronal damage induced by nvestigated the effects of long-term exposure to high corticosterone levels on AK1 activity, AK1 mRNA expression, and energy levels in cultured hippocampal neurons. The results show that long-term exposure to high corticosterone levels induces a reduction of the cultured hippocampal neuron viability, significantly reduces energy levels, and causes a time-dependant re- duction of the AK1 activity. These findings indicate that changes in the AK system might be the mechanism underlying neuronal damage induced by long-term exposure to high corticosterone levels.
Previous studies have shown that mice experiencing cerebral ischemia reperfusion （CIR） and stress can serve as a model of post stroke depression （PSD）. The present study verified the acute antidepressant effects of radix puerariae extract （PE） on PSD mice through behavior and gene expression experiments. CIR was found to reduce the sucrose consumption and tyrosine hydroxylase （TH） gene expression. PE administration after CIR surgery was observed to significantly enhance the mRNA expression of TH in the hippocampus compared with the PSD group on Day 0 and Day 3 postsurgery. These findings indicate that PE contributes to the amelioration of behavior response in PSD mice, which is closely related with the protective effects of catecholamine synthesize against CIR brain damage.
