A metabolic fragment of bradykinin, Arg-Pro-Pro-Gly-Phe, protects against the deleterious effects of lipopolysaccharide in rats

Citation
Ta. Morinelli et al., A metabolic fragment of bradykinin, Arg-Pro-Pro-Gly-Phe, protects against the deleterious effects of lipopolysaccharide in rats, J PHARM EXP, 296(1), 2001, pp. 71-76
Citations number
37
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
ISSN journal
00223565 → ACNP
Volume
296
Issue
1
Year of publication
2001
Pages
71 - 76
Database
ISI
SICI code
0022-3565(200101)296:1<71:AMFOBA>2.0.ZU;2-5
Abstract
Extensive research has provided few therapeutic agents for the treatment of septicemia. Bradykinin, an endogenous vasodepressor hormone, is a key medi ator in the hypotension seen with septicemia. The present investigation sho ws that a stable metabolic fragment of bradykinin, arginine-proline-proline -glycine-phenylalanine (RPPGF), prevents the deleterious effects of endotox in [lipopolysaccharide (LPS); a component of the membrane of Gram negative bacteria], the signaling agent responsible for the effects of septicemia, i n both anesthetized rats and in isolated rat aortic segments. Survival time of rats treated with LPS (12 mg/kg) was significantly (p< 0.05) prolonged by pretreatment with RPPGF [140.3 +/- 16 min (n = 10)] compared with rats r eceiving saline and LPS [93.2 +/- 8 min (n = 39)]. Prolongation of survival was not seen when rats were pretreated with either bradykinin or with PRGF P (proline-arginine-glycine-phenylalanine- proline). Isolated aortic segmen ts treated with LPS (30 <mu>g/ml) showed a significantly reduced ability to contract in response to phenylephrine compared with control segments not r eceiving LPS. Pretreatment of the segments with RPPGF significantly reverse d the LPS-induced reduction in contractile response of the segments. Remova l of the endothelial layer did not alter the protection provided by RPPGF. These results demonstrate the ability of a stable metabolic fragment of bra dykinin, RPPGF, to protect against the deleterious effects produced by LPS. The findings presented here may provide the basis for a new developmental area for novel therapeutic agents in the treatment of septicemia.