Different vasoactive effects of chronic endothelial and neuronal NO-synthase inhibition in young Wistar rats View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-06-28

AUTHORS

Sona Cacanyiova, Andrea Berenyiova, Magdalena Malekova, Frantisek Kristek, Ima Dovinova, Peter Krenek, Lenka Pivackova, Ivana Pifkova

ABSTRACT

While the unequivocal pattern of endothelial nitric oxide synthase (eNOS) inhibition in cardiovascular control is recognized, the role of NO produced by neuronal NOS (nNOS) remains unclear. The aim of this study was to compare the effects of chronic treatment with 7-nitroindazole (7-NI, nNOS inhibitor) and NG-nitro-l-arginine methylester (l-NAME, general and predominantly eNOS inhibitor) on cardiovascular system of young normotensive rats. Wistar rats (4 weeks old) were used: controls and rats administered either 7-NI (10 mg/kg bw/day) or l-NAME (50 mg/kg bw/day) in drinking water for 6 weeks. The systolic blood pressure (sBP) was measured by plethysmographic method, and the vasoactivity of isolated arteries was recorded. 7-NI-treatment did not affect sBP; however, the sBP was increased after l-NAME-treatment. l-NAME inhibited acetylcholine-induced relaxation of thoracic aorta (TA), whereas it remained unchanged after 7-NI-treatment. The response of TA to sodium nitroprusside was increased in both experimental groups. The expression of eNOS and nNOS in TA was unchanged in both experimental groups, whereas the activity of NOS was decreased in l-NAME-treated group. Noradrenaline- and angiotensin II-induced contractions of TA were reduced in l-NAME-treated group; however, the contractions remained unchanged in 7-NI-treated group. In all groups, the endogenous angiotensin II participated in adrenergic contraction of TA; this contribution was significantly increased in l-NAME-treated group. Neurogenic contractions in mesenteric artery (MA) remained unchanged after 7-NI-treatment, but increased after l-NAME-treatment. Results show that NO deficiency induced by administration of 7-NI and l-NAME had different cardiovascular effects: eNOS and nNOS triggered distinct signaling pathways in young normotensive rats. More... »

PAGES

749-760

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s13105-014-0343-2

DOI

http://dx.doi.org/10.1007/s13105-014-0343-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1030827070

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24972660


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