Protective Effects of Yinaokang Capsule on Blood-brain Barrier and Influence on Expression of ZO-1 Protein after Thrombolysis Therapy in Cerebral Ischemia Rats
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Protective Effects of Yinaokang Capsule on Blood-brain Barrier and Influence on Expression of ZO-1 Protein after Thrombolysis Therapy in Cerebral Ischemia Rats
Chinese Journal of Experimental Traditional Medical FormulaeVol. 19, Issue 11, Pages: 268-271(2013)
LI Yue, SUN Jing-bo, HUANG Yan. Protective Effects of Yinaokang Capsule on Blood-brain Barrier and Influence on Expression of ZO-1 Protein after Thrombolysis Therapy in Cerebral Ischemia Rats[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(11): 268-271.
DOI:
LI Yue, SUN Jing-bo, HUANG Yan. Protective Effects of Yinaokang Capsule on Blood-brain Barrier and Influence on Expression of ZO-1 Protein after Thrombolysis Therapy in Cerebral Ischemia Rats[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(11): 268-271. DOI: 10.11653/syfj2013110268.
Protective Effects of Yinaokang Capsule on Blood-brain Barrier and Influence on Expression of ZO-1 Protein after Thrombolysis Therapy in Cerebral Ischemia Rats
Objective: To investigate the effects of Yinaokang capsule (YC) on blood-brain barrier opening and expression of zonular occludens protein (ZO-1 protein) after thrombolysis therapy by recombinant tissue type plasminogen activator (rt-PA) in rats. Method: The rats were randomly divided into sham operation group
thrombolysis group
YC low dose group (1 g·kg-1daily for 3 d)
YC high dose group (3 g·kg-1daily for 3 d). Model of middle cerebral artery occlusion in rats was established by embolizing left middle cerebral artery with autologous blood clots. The permeability of the brain-blood barrier was observed with Evan's blue (EB) with spectrophotometer and the expression of ZO-1 protein was detected by Western blot. Result: Compared with the sham group
EB leakage in brain tissue was increased significantly and the expression of ZO-1 protein was decreased obviously in all other groups. Compared with the thrombolysis group
the EB leakage showed no difference in YC low dose group and increased in the high dose YC group; the expression of ZO-1 protein was increased significantly in both YC groups. Compared with the low dose YC group
the EB leakage in the high dose YC group was decreased
and the expression of ZO-1 protein in the high dose YC group was increased. Conclusion: YC could attenuate the breakdown of brain-blood barrier after thrombolysis therapy. Its mechanisms may be associated with up-regulated expression of ZO-1 protein.