Zhao Li-Fang, Jiang Rui, Ji Peng, Wang Ru-Rong
Department of Anesthesiology, West China Hospital, Sichuan University, Chengdu 610041, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2012 Sep;43(5):666-9.
To study the effect of calcitonin gene-related peptide (CGRP) receptor on the expression of nuclear factor-kappa b (NF-kappa b) in rat lung after ischemia reperfusion injury.
Thirty-two adult male Sprague Dawley rats were divided into four groups (8 per group) as follows: sham group (sham thoracotomy), IR group (occlusion of the left pulmonary hilus for 0.5 h followed by reperfusion for 4 h), another two groups were pretreated with CGRP or CGRP8-37 (a CGRP receptor antagonist). Arterial blood was collected at the end of reperfusion to test blood gas, arterial oxygen pressure (PaO2) and alveolar arterial oxygen difference (A-aDO2). Lung tissue was collected to measure the expression level of NF-kappa b mRNA by using RT-PCR. Light microscopic changes of lung tissue were also examined.
Compared with sham group, rats in the IR group had poorer gas exchange (lower PaO2, higher A-aDO2), upregulation of NF-kappa b mRNA expression (P < 0.05) and more severe histological injury. Pretreatment with CGRP improved gas exchange function, significantly decreased NF-kappa b mRNA expression (P < 0.05 versus IR and CGRP837 groups). Administration of CGRP also attenuated IR-induced pathological lesions. The pretreatment of CGRP8-37 showed the opposite results to those of CGRP.
CGRP receptor plays an important protective role in lung IR injury, which is closely related to the downregulation of NF-kappa b mRNA.
研究降钙素基因相关肽(CGRP)受体对大鼠肺缺血再灌注损伤后核因子-κB(NF-κB)表达的影响。
将32只成年雄性Sprague Dawley大鼠分为四组(每组8只),如下:假手术组(假开胸手术)、IR组(左肺门阻断0.5小时后再灌注4小时),另外两组分别用CGRP或CGRP8-37(一种CGRP受体拮抗剂)预处理。再灌注结束时采集动脉血检测血气、动脉血氧分压(PaO2)和肺泡动脉氧分压差(A-aDO2)。采集肺组织,采用RT-PCR法检测NF-κB mRNA的表达水平。同时观察肺组织的光镜变化。
与假手术组相比,IR组大鼠气体交换功能较差(PaO2较低,A-aDO2较高),NF-κB mRNA表达上调(P<0.05),组织学损伤更严重。CGRP预处理改善了气体交换功能,显著降低了NF-κB mRNA表达(与IR组和CGRP837组相比,P<0.05)。给予CGRP还减轻了IR诱导的病理损伤。CGRP8-37预处理的结果与CGRP相反。
CGRP受体在肺IR损伤中起重要保护作用,这与NF-κB mRNA的下调密切相关。