Fan Qinlin,Jiao Yan,Liu Guojun,Zhou Zhenhua,Zhang Bo,Chen Lin,Gan Lixia,Chen Kangning.Relationship between HAX-1 expression and neuron apoptosis after cerebral ischemia reperfusion injury in rats[J].J Amry Med Univ (J Third Mil Med Univ),2010,32(06):584-587.
Fan Qinlin,Jiao Yan,Liu Guojun,Zhou Zhenhua,Zhang Bo,Chen Lin,Gan Lixia,Chen Kangning.Relationship between HAX-1 expression and neuron apoptosis after cerebral ischemia reperfusion injury in rats[J].J Amry Med Univ (J Third Mil Med Univ),2010,32(06):584-587.DOI:
Relationship between HAX-1 expression and neuron apoptosis after cerebral ischemia reperfusion injury in rats
Objective To investigate the relationship between HS1-associated protein X-1 (HAX-1) expression and neuron apoptosis in rats after global cerebral ischemia reperfusion injury. Methods Rats were subjected to global cerebral ischemia reperfusion injury through fourvessel occlusion
and then the experimental rats were divided into 5 groups
normal group (NC)
6
24
48 and 72 h post injury groups (n=5 for each group). Immunohistochemistry and TUNEL were used to detect HAX-1 expression and activated Caspase-3
and cell apoptosis in cortex of rats. Results The expression level of HAX1 in ischemic cortex was peaked at 6 h (37.60±3.45)
then decreased at 24
48 and 72 h (11.40±1.14
10.40±1.52
and 9.80±1.30 respectively)
to an extend lower than the normal level (P0.01). The expression of Caspase-3 in ischemic cortex was up-regulated after global cerebral ischemia reperfusion injury in rats with the prolongation of injury time (72.80±5.49
106.20±6.91
129.00±19.74
and 166.20±15.32 respectively for 6
24
48 and 72 h post injury). The number of apoptotic cells was increased obviously with the elapse of time (92.00±9.06
133.80±10.64
157.00±10.83
and 187.80±14.96 respectively for 6
24
48 and 72 h post injury
P0.01). Conclusion The expression of HAX-1 reachs a peak in a short time after global ischemia reperfusion injury
suggesting it may be involved in the anti-apoptosis of neuron apoptosis. With the elapse of injury time
its expression is decreased and associated with the increase of apoptotic cells.