ABSTRACT
<p><b>OBJECTIVE</b>To investigate the effect of Buyang Huanwu Decoction (BYHWD) and the different combinations of its ingredients on neurogenesis following ischemic stroke in rats.</p><p><b>METHODS</b>The model rats of ischemic stroke was established by blocking cerebral media artery with electrocoagulation through craniectomy, and electric stimulation, given from 24 h after blocking, 2 h daily for 15 successive days. They were divided into four groups, Group A treated with saline, Group B treated with BYHWD, Group C treated with BYHWD but earthworm subtracted, and Group D treated with Danggui Buxue Decoction (DGBXD). The expression of 5-bromodeoxyuridine (BrdU) in cerebral tissue was determined by immunohistochemical method.</p><p><b>RESULTS</b>Large amount of BrdU immunoreactive cells presented in the hippocampal region of rats in Group B and C, densely arranged, partial in cluster, with the figure significantly different to that in Group A (P < 0.01), and the amount in the ischemic side was significantly more than that in the opposite side (P < 0.05). While comparing between Group A and D, the amount of BrdU immunoreactive cells in the hippocampal region showed insignificant difference (P > 0.05).</p><p><b>CONCLUSION</b>BYHWD has a effect in promoting neurogenesis better than DGBXD.</p>
Subject(s)
Animals , Male , Rats , Bromodeoxyuridine , Metabolism , Drugs, Chinese Herbal , Pharmacology , Therapeutic Uses , Hippocampus , Metabolism , Pathology , Immunohistochemistry , Infarction, Middle Cerebral Artery , Drug Therapy , Neurons , Metabolism , Pathology , Neuroprotective Agents , Pharmacology , Therapeutic Uses , Phytotherapy , Random Allocation , Rats, WistarABSTRACT
<p><b>OBJECTIVE</b>To examine the effect of Buyanghuanwu decoction (BYHWD) in inducing nerve proliferation in rats with sequelae of ischemic stroke.</p><p><b>METHODS</b>A rat model of ischemic stroke sequelae was established by means of craniectomy in which the right common carotid artery was ligated with 4-0 silk thread followed by cauterization of the right middle cerebral artery. Programmed electric shock was administered 24 h after the onset of ischemic stroke for 2 h daily for 20 consecutive days. The rats in sham operation group were not subjected to ligation of the right common carotid artery or right middle cerebral artery occlusion. The rats in the treatment groups were given oral BYHWD for 15 consecutive days. All the rats received repeated intraperitoneal injections of the cell proliferation-specific marker 5-bromodeoxyuridine (BrdU), and the intake of BrdU in the cerebral tissues was determined by immunohistochemistry.</p><p><b>RESULTS</b>The number of BrdU-immunoreactive cells in the cerebral tissues of BYHWD-treated rats was significantly greater than that in the untreated model group.</p><p><b>CONCLUSION</b>BYHWD can promote nerve proliferation in rats with ischemic stroke sequelae.</p>