Effects of Oleamide on the Vasomotor Responses in the Rat.
| Autor: | Hernández-Díaz C; Hospital Universitario de Burgos, Burgos, Spain.; Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de Mexico, Distrito Federal, Mexico., Juárez-Oropeza MA; Departamento de Bioquímica, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de México, Distrito Federal, Mexico., Mascher D; Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de Mexico, Distrito Federal, Mexico., Pavón N; Departamento de Farmacología, Instituto Nacional de Cardiología, Ciudad de Mexico, Mexico., Regla I; Laboratorio Síntesis de Fármacos, UMIEZ, Facultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de México, Ciudad de México, Mexico., Paredes-Carbajal MC; Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de Mexico, Distrito Federal, Mexico. |
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| Jazyk: | angličtina |
| Zdroj: | Cannabis and cannabinoid research [Cannabis Cannabinoid Res] 2020 Feb 27; Vol. 5 (1), pp. 42-50. Date of Electronic Publication: 2020 Feb 27 (Print Publication: 2020). |
| DOI: | 10.1089/can.2019.0014 |
| Abstrakt: | Introduction: Cardiovascular effects of endocannabinoids (eCBs) have generated considerable interest since it has been suggested that the eCB system could become the new pharmacological target, either by blocking its activity or by promoting its effects on several cardiovascular diseases such as hypovolemic and septic shock or hypertension. The purpose of this study was to examine the effects of oleamide on several vasomotor responses in adult rats. Materials and Methods: Blood pressure (BP) was measured both directly and indirectly. Coronary flow was quantified with Langendorf preparation, and the vasomotor responses induced by oleamide were analyzed in the aortic rings. Results: Oleamide induced a decrease in BP, by both direct and indirect methods, which were dose dependent. An increase in coronary flow was observed with Langendorf preparation depending on the dose. Oleamide produced a vasodilator response in aortic rings pre-contracted with phenylephrine (10 -5 M), which was concentration and endothelium dependent. This relaxing effect was of minor magnitude than that induced with the same dose on BP. L-NAME did not modify these effects. However, indomethacin induced a shift to the left of the concentration-response curve to oleamide and an increase in the magnitude of maximum vasodilation in rings with endothelium. Oleamide produced the maximal relaxant response at 10 -5 M concentration. Conclusions: Oleamide has both in vivo and in vitro vasodilator effects. Vasodilator effects could be mediated by compounds synthesized/released by the endothelium (hyperpolarizing factor) or acting directly on vascular smooth muscle in aortic rings. The TRPV1 and CB1R receptors could mediate these effects. Finally, the results suggest that oleamide probably induces the synthesis/release of a vasoconstrictor prostanoid. Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. (Copyright 2020, Mary Ann Liebert, Inc., publishers.) |
| Databáze: | MEDLINE |
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