Publication: The effect of agmatine on the vascular reactivity in streptozotocin-diabetic rats
| dc.contributor.authors | Ozyazgan, S; Bicakci, B; Ozaydin, A; Denizbasi, A; Unluer, EE; Akkan, AG | |
| dc.date.accessioned | 2022-03-12T17:17:13Z | |
| dc.date.accessioned | 2026-01-10T17:49:45Z | |
| dc.date.available | 2022-03-12T17:17:13Z | |
| dc.date.issued | 2003 | |
| dc.description.abstract | Aim: We investigated the vascular effects of agmatine (decarboxylated arginine = AGM), an endogenous ligand for alpha(2)-adrenoceptors and imidazoline receptors, present in endothelium and smooth muscle, using the diabetic rat aortae. Materials and methods: Studies were performed in control group (0.2 ml i.p. saline, n = 10), streptozotocin (STZ)-diabetic control group (60 mg kg(-1) STZ i.p., n = 10), agmatine (AGM)-control group (5 mg kg(-1) day(-1) i.p. AGM for 1 month, n = 10), citrate-control group (0.2 ml 0.01 M, n = 10), insulin-treated diabetic group ((3 U kg(-1) NPH + 1 U kg(-1) regular insulin) twice per day, for 1 month, n = 10) and AGM-treated diabetic group (5 mg kg(-1) day(-1) i.p. for 1 month, n = 10). All values are expressed as means +/-S.E.M. Statistical analysis of the data was performed using ANOVA followed by Tukey multiple comparisons test. Results: One-month AGM-treatment significantly decreased the blood glucose levels of diabetic rats (502 +/- 44 mg dl(-1) to 343 +/- 31 mg dl(-1), P < 0.001). Fast, slow and total components of responses to noradrenaline in all the experimental groups were not significantly affected by AGM-treatment. AGM reversed the decreased responses of acetylcholine (pD(2) and Inh.%, P < 0.001 and P < 0.05) in diabetic rats although it did not affect the responses of sodium nitroprusside in all groups. The contraction values of KCl in all groups were not affected by AGM-treatment. Conclusion: AGM-treatment could improve the increased blood glucose level, reverse the endothelial dysfunction and normalize the endothelium-dependent relaxation responses in STZ-diabetic rats. (C) 2003 Elsevier Science Ltd. All rights reserved. | |
| dc.identifier.doi | 10.1016/S1043-6618(03)00101-4 | |
| dc.identifier.issn | 1043-6618 | |
| dc.identifier.pubmed | 12798665 | |
| dc.identifier.uri | https://hdl.handle.net/11424/227796 | |
| dc.identifier.wos | WOS:000183923400002 | |
| dc.language.iso | eng | |
| dc.publisher | ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD | |
| dc.relation.ispartof | PHARMACOLOGICAL RESEARCH | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | agmatine | |
| dc.subject | diabetes | |
| dc.subject | vascular reactivity | |
| dc.subject | streptozotocin | |
| dc.subject | SMOOTH-MUSCLE | |
| dc.subject | NITRIC-OXIDE | |
| dc.subject | EXTRACELLULAR CALCIUM | |
| dc.subject | ALPHA ADRENOCEPTORS | |
| dc.subject | ENDOTHELIUM | |
| dc.subject | AORTA | |
| dc.subject | CONTRACTION | |
| dc.subject | RESPONSES | |
| dc.subject | INSULIN | |
| dc.subject | RELAXATION | |
| dc.title | The effect of agmatine on the vascular reactivity in streptozotocin-diabetic rats | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 138 | |
| oaire.citation.issue | 2 | |
| oaire.citation.startPage | 133 | |
| oaire.citation.title | PHARMACOLOGICAL RESEARCH | |
| oaire.citation.volume | 48 |
