Siebeck M, Schorr M, Spannagl E, Lehner M, Fritz H, Cheronis J C, Whalley E T
Department of Surgery, Klinikum Innenstadt, Ludwig-Maximilians University, Munich, Germany.
Immunopharmacology. 1998 Jul;40(1):49-55. doi: 10.1016/s0162-3109(98)00035-6.
Bradykinin (BK) and related kinins are potent inflammatory mediators produced during acute and chronic inflammation. The effects of these kinins are mediated via the stimulation of either a B2 or a B1 receptor. The B1 receptor is not normally present but its expression can be induced within 4 h by a variety of noxious stimuli, specifically, gram-negative bacteria or bacterial lipopolysaccharide (LPS) given to healthy animals. This study compared the cardiovascular response of healthy pigs and pigs diagnosed with a pre-existing spontaneously acquired infection to BK, a B2 receptor agonist, and des-Arg9-BK, a B1 receptor agonist. Eighty-eight percent of the animals diagnosed with an established infection based on a standardized clinical evaluation demonstrated increased sensitivity and responsiveness to des-Arg9-BK but normal responsiveness to BK and acetylcholine. In contrast, only 15% of healthy animals showed elevated responses to des-Arg9-BK. The response to des-Arg9-BK and BK in each group was characterised as B1 and B2, respectively, using the selective B1 and B2 antagonists Lys0-Leu8-des-Arg9-BK and Hoe 140, respectively. This study demonstrates the existence and function of the B1 receptor in animals with a previously acquired infection. These observations lend validity to animal experiments with LPS infusion in order to model bacterial inflammation.
缓激肽(BK)及相关激肽是在急慢性炎症过程中产生的强效炎症介质。这些激肽的作用是通过刺激B2或B1受体介导的。B1受体通常不存在,但在多种有害刺激下,特别是给健康动物注射革兰氏阴性菌或细菌脂多糖(LPS)后,其表达可在4小时内被诱导。本研究比较了健康猪和被诊断为已存在自发获得性感染的猪对BK(一种B2受体激动剂)和去精氨酸9 - 缓激肽(des - Arg9 - BK,一种B1受体激动剂)的心血管反应。基于标准化临床评估,88%被诊断为已确诊感染的动物对去精氨酸9 - 缓激肽表现出敏感性和反应性增加,但对BK和乙酰胆碱的反应正常。相比之下,只有15%的健康动物对去精氨酸9 - 缓激肽的反应增强。分别使用选择性B1和B2拮抗剂Lys0 - Leu8 - des - Arg9 - BK和Hoe 140,将每组对去精氨酸9 - 缓激肽和BK的反应分别表征为B1和B2反应。本研究证明了在先前获得感染的动物中B1受体的存在及其功能。这些观察结果为通过输注LPS来模拟细菌炎症的动物实验提供了有效性依据。