Clementi G, Amico-Roxas M, Caruso A, Catena Cutuli V M, Prato A, Maugeri S, de Bernardis E, Scapagnini U
Institute of Pharmacology, University of Catania School of Medicine, Italy.
Life Sci. 1994;54(8):PL119-24. doi: 10.1016/0024-3205(94)90011-6.
The anti-inflammatory activity of calcitonin gene-related peptide (CGRP) has been studied in cutaneous inflammation induced by croton oil (CO), arachidonic acid (AA), tetradecanoylphorbol acetate (TPA) or cantharidin (CA). Our results show that mouse ear inflammation induced by CO, AA or TPA is decreased by topical administration of CGRP, whereas that induced by CA is not affected. The dose-response and temporal analysis of CGRP effect show that the maximal activity is present at the dose of 30 pmol/ear and when administered 30 min after the irritating agent. Moreover, pretreatment with capsaicin is able to mimic the anti-inflammatory effect of exogenous CGRP, while simultaneous administration of CGRP and capsaicin produces a reduced response. Our results suggest that CGRP released from sensory.
已在巴豆油(CO)、花生四烯酸(AA)、十四酰佛波醇乙酸酯(TPA)或斑蝥素(CA)诱导的皮肤炎症中研究了降钙素基因相关肽(CGRP)的抗炎活性。我们的结果表明,局部施用CGRP可减轻由CO、AA或TPA诱导的小鼠耳部炎症,而由CA诱导的炎症则不受影响。CGRP作用的剂量反应和时间分析表明,在剂量为30 pmol/耳且在刺激剂施用后30分钟给药时存在最大活性。此外,用辣椒素预处理能够模拟外源性CGRP的抗炎作用,而同时施用CGRP和辣椒素则产生减弱的反应。我们的结果表明,感觉神经释放的CGRP。