PMID- 12522068 OWN - NLM STAT- MEDLINE DCOM- 20030715 LR - 20181113 IS - 0007-1188 (Print) IS - 0007-1188 (Linking) VI - 138 IP - 1 DP - 2003 Jan TI - Up-regulation of kinin B1 receptor in the lung of streptozotocin-diabetic rat: autoradiographic and functional evidence. PG - 13-22 AB - 1 The function and autoradiographic binding expression of kinin B(1) receptors were evaluated in the lungs of Streptozotocin (STZ)-diabetic rats. 2 The intrapleural injection (i.pl.) of des-Arg(9)-bradykinin (des-Arg(9)-BK) (50 and 100 nmol per site), a selective B(1) receptor agonist, increased time-dependently the mononuclear and neutrophil cells influx in the pleural cavity of rats treated with STZ (65 mg kg(-1), i.p., 4 days earlier). This effect was significantly less in control rats. 3 The influx of mononuclear and polymorphonuclear neutrophil cells induced by des-Arg(9)-BK was significantly inhibited by two B(1) receptor antagonists (des-Arg(10)-Hoe140 or R-715, 100 nmol per site, 5 min earlier), but not by two B(2) receptor antagonists (Hoe140, 10 nmol or NPC 18884, 100 nmol per site, 5 min earlier). However, Hoe140 prevented the higher basal leukocyte influx seen in STZ-diabetic rats. 4 Leukocyte infiltration induced by des-Arg(9)-BK in STZ-diabetic rats was significantly reduced after treatment with insulin (2 U per day, s.c. over 4 days) or with an anti-PMN antibody (0.1 ml of a 1 : 20 dilution, i.pl. 5 min earlier). 5 Specific B(1) receptor binding sites were seen in lung sections from both control and STZ-diabetic rats, yet the density of labelling was much greater in diabetic rats and particularly after intrapleural injection of des-Arg(9)-BK. Treatment with insulin or with the anti-PMN antibody markedly reduced B(1) receptor binding sites occurring after the injection of des-Arg(9)-BK in STZ-diabetic rats. 6 Data suggest that the B(1) receptor is up-regulated in the lungs of STZ-diabetic rats, and its activation increases leukocyte infiltration into the pleural cavity. The overexpression of B(1) receptors seems to depend on neutrophils influx and appears to be associated with hyperglycaemia. FAU - Vianna, Rose Mari J AU - Vianna RM AD - Department of Physiology, Faculty of Medicine, Universite de Montreal, Montreal, C.P. 6128, Succursale centre-ville, Montreal, Quebec, Canada H3C 3J7. FAU - Ongali, Brice AU - Ongali B FAU - Regoli, Domenico AU - Regoli D FAU - Calixto, Joao Batista AU - Calixto JB FAU - Couture, Rejean AU - Couture R LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - Br J Pharmacol JT - British journal of pharmacology JID - 7502536 RN - 0 (Receptor, Bradykinin B1) RN - 0 (Receptors, Bradykinin) SB - IM MH - Animals MH - Autoradiography MH - Cell Movement/drug effects/physiology MH - Diabetes Mellitus, Experimental/*metabolism MH - Leukocytes/cytology/drug effects/metabolism MH - Lung/cytology/drug effects/*metabolism MH - Male MH - Rats MH - Rats, Wistar MH - Receptor, Bradykinin B1 MH - Receptors, Bradykinin/agonists/*biosynthesis MH - Up-Regulation/drug effects/*physiology PMC - PMC1573626 EDAT- 2003/01/11 04:00 MHDA- 2003/07/16 05:00 PMCR- 2004/01/01 CRDT- 2003/01/11 04:00 PHST- 2003/01/11 04:00 [pubmed] PHST- 2003/07/16 05:00 [medline] PHST- 2003/01/11 04:00 [entrez] PHST- 2004/01/01 00:00 [pmc-release] AID - 0704999 [pii] AID - 10.1038/sj.bjp.0704999 [doi] PST - ppublish SO - Br J Pharmacol. 2003 Jan;138(1):13-22. doi: 10.1038/sj.bjp.0704999.