Apoptosis--dependent acute pulmonary injury after intratracheal instillation of angiotensin Ⅱ
Zhuang Jiaju, Li Xiaopeng, Uhal B D, Yian K R
Department of Physiology,Bethune Military Medical College.Shijiazhuang 050081,Hebei;USA
Abstract
To test the hypothesis that exogenous purified angiotensin Ⅱ(ANG) might cause apoptosis of alveolar epithelial cells(AECs) and acute lung injury,male Wistar rats were intratracheally instilled with purified ANG(10 #mu#mol/L),ANG plus the caspase inhibitor ZVAD-fmk(60 #mu#mol/L),ANG plus the ANG receptor AT1 antagonist losartan(LOS,100 #mu#mol/L) or sterile phosphate-buffered saline(PBS) vehicle alone.Six or 20 h later,the lungs were lavaged in situ for determination of bronchoalveolar lavage(BAL) fluid content of hemoglobin(Hb) and fluorescent(BODIPY)-albumin,a bolus of which was injected intravenously 15 min prior to BAL.Terminal deoxynucleotidyl transferase-mediated nick-end labeling(TUNEL) revealed that instillation of ANG,but not PBS alone,increased labeling of fragmented DNA in bronchiolar epithelial cells and in AECs(P<0.05) at 6 h post-ANG.Increased TUNEL was abrogated by concurrent instillation of ZVAD-fmk or LOS.Significant increased numbers of caspase-positive cells were observed by anti-caspase 3 immunolabeling after instillation of ANG(P<0.01);the same doses of LOS or ZVAD-fmk that blocked TUNEL also blocked the activation of caspase 3(P<0.01).Intratracheal instillation of ANG also remarkably increased BAL BODIPY-albumin(P< 0.01) and Hb(P<0.05),both of which were eliminated by ZVAD-fmk or LOS.These data indicate that exposure of AECs to ANG in vivo is sufficient to induce apoptosis and alveolar epithelial barrier injury mediated by ANG receptor AT1.
Key words: Apoptosis;alveolar epithelial cell;acute pulmonary injury;type Ⅱ pneumocyte
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Citing This Article:
Zhuang Jiaju, Li Xiaopeng, Uhal B D, Yian K R. Apoptosis--dependent acute pulmonary injury after intratracheal instillation of angiotensin Ⅱ. Acta Physiol Sin 2008; 60 (6): 715-722 (in Chinese with English abstract).