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1-Nitro-2-phenylethane, the main constituent of the essential oil of Aniba canelilla, elicits a vago-vagal bradycardiac and depressor reflex in normotensive rats.
Eur J Pharmacol. 2010 Jul 25; 638(1-3):90-8.EJ

Abstract

Previously, it was shown that intravenous (i.v.) treatment with the essential oil of Aniba canelilla (EOAC) elicited a hypotensive response that is due to active vascular relaxation rather than to the withdrawal of sympathetic tone. The present study investigated mechanisms underlying the cardiovascular responses to 1-nitro-2-phenylethane, the main constituent of the EOAC. In pentobarbital-anesthetized normotensive rats, 1-nitro-2-phenylethane (1-10mg/kg, i.v.) elicited dose-dependent hypotensive and bradycardiac effects which were characterized in two periods (phases 1 and 2). The first rapid component (phase 1) evoked by 1-nitro-2-phenylethane (10mg/kg) was fully abolished by bilateral vagotomy, perineural treatment of both cervical vagus nerves with capsaicin (250 microg/ml) and was absent after left ventricle injection. However, pretreatment with capsazepine (1mg/kg, i.v.) or ondansetron (30 microg/kg, i.v.) did not alter phase 1 of the cardiovascular responses to 1-nitro-2-phenylethane (10mg/kg, i.v.). In conscious rats, 1-nitro-2-phenylethane (1-10mg/kg, i.v.) evoked rapid hypotensive and bradycardiac (phase 1) effects that were fully abolished by methylatropine (1mg/kg, i.v.). It is concluded that 1-nitro-2-phenylethane induces a vago-vagal bradycardiac and depressor reflex (phase 1) that apparently results from the stimulation of vagal pulmonary rather than cardiac C-fiber afferents. The transduction mechanism of the 1-nitro-2-phenylethane excitation of C-fiber endings is not fully understood and does not appear to involve activation of either Vanilloid TPRV(1) or 5-HT(3) receptors. The phase 2 hypotensive response to 1-nitro-2-phenylethane seems to result, at least in part, from a direct vasodilatory effect since 1-nitro-2-phenylethane (1-300 microg/ml) induced a concentration-dependent reduction of phenylephrine-induced contraction in rat endothelium-containing aorta preparations.

Authors+Show Affiliations

Departamento de Fisiologia e Farmacologia, Universidade Federal de Pernambuco, Recife, PE, Brazil.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

20406629

Citation

de Siqueira, Rodrigo José Bezerra, et al. "1-Nitro-2-phenylethane, the Main Constituent of the Essential Oil of Aniba Canelilla, Elicits a Vago-vagal Bradycardiac and Depressor Reflex in Normotensive Rats." European Journal of Pharmacology, vol. 638, no. 1-3, 2010, pp. 90-8.
de Siqueira RJ, Macedo FI, Interaminense Lde F, et al. 1-Nitro-2-phenylethane, the main constituent of the essential oil of Aniba canelilla, elicits a vago-vagal bradycardiac and depressor reflex in normotensive rats. Eur J Pharmacol. 2010;638(1-3):90-8.
de Siqueira, R. J., Macedo, F. I., Interaminense, L. d. e. . F., Duarte, G. P., Magalhães, P. J., Brito, T. S., da Silva, J. K., Maia, J. G., Sousa, P. J., Leal-Cardoso, J. H., & Lahlou, S. (2010). 1-Nitro-2-phenylethane, the main constituent of the essential oil of Aniba canelilla, elicits a vago-vagal bradycardiac and depressor reflex in normotensive rats. European Journal of Pharmacology, 638(1-3), 90-8. https://doi.org/10.1016/j.ejphar.2010.03.060
de Siqueira RJ, et al. 1-Nitro-2-phenylethane, the Main Constituent of the Essential Oil of Aniba Canelilla, Elicits a Vago-vagal Bradycardiac and Depressor Reflex in Normotensive Rats. Eur J Pharmacol. 2010 Jul 25;638(1-3):90-8. PubMed PMID: 20406629.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - 1-Nitro-2-phenylethane, the main constituent of the essential oil of Aniba canelilla, elicits a vago-vagal bradycardiac and depressor reflex in normotensive rats. AU - de Siqueira,Rodrigo José Bezerra, AU - Macedo,Francisco Igor Bulcão, AU - Interaminense,Leylliane de Fátima Leal, AU - Duarte,Gloria Pinto, AU - Magalhães,Pedro Jorge Caldas, AU - Brito,Teresinha Silva, AU - da Silva,Joyce Kelly Rosário, AU - Maia,José Guilherme Soares, AU - Sousa,Pergentino José da Cunha, AU - Leal-Cardoso,José Henrique, AU - Lahlou,Saad, Y1 - 2010/04/18/ PY - 2009/11/27/received PY - 2010/03/06/revised PY - 2010/03/31/accepted PY - 2010/4/22/entrez PY - 2010/4/22/pubmed PY - 2010/9/29/medline SP - 90 EP - 8 JF - European journal of pharmacology JO - Eur J Pharmacol VL - 638 IS - 1-3 N2 - Previously, it was shown that intravenous (i.v.) treatment with the essential oil of Aniba canelilla (EOAC) elicited a hypotensive response that is due to active vascular relaxation rather than to the withdrawal of sympathetic tone. The present study investigated mechanisms underlying the cardiovascular responses to 1-nitro-2-phenylethane, the main constituent of the EOAC. In pentobarbital-anesthetized normotensive rats, 1-nitro-2-phenylethane (1-10mg/kg, i.v.) elicited dose-dependent hypotensive and bradycardiac effects which were characterized in two periods (phases 1 and 2). The first rapid component (phase 1) evoked by 1-nitro-2-phenylethane (10mg/kg) was fully abolished by bilateral vagotomy, perineural treatment of both cervical vagus nerves with capsaicin (250 microg/ml) and was absent after left ventricle injection. However, pretreatment with capsazepine (1mg/kg, i.v.) or ondansetron (30 microg/kg, i.v.) did not alter phase 1 of the cardiovascular responses to 1-nitro-2-phenylethane (10mg/kg, i.v.). In conscious rats, 1-nitro-2-phenylethane (1-10mg/kg, i.v.) evoked rapid hypotensive and bradycardiac (phase 1) effects that were fully abolished by methylatropine (1mg/kg, i.v.). It is concluded that 1-nitro-2-phenylethane induces a vago-vagal bradycardiac and depressor reflex (phase 1) that apparently results from the stimulation of vagal pulmonary rather than cardiac C-fiber afferents. The transduction mechanism of the 1-nitro-2-phenylethane excitation of C-fiber endings is not fully understood and does not appear to involve activation of either Vanilloid TPRV(1) or 5-HT(3) receptors. The phase 2 hypotensive response to 1-nitro-2-phenylethane seems to result, at least in part, from a direct vasodilatory effect since 1-nitro-2-phenylethane (1-300 microg/ml) induced a concentration-dependent reduction of phenylephrine-induced contraction in rat endothelium-containing aorta preparations. SN - 1879-0712 UR - https://www.unboundmedicine.com/medline/citation/20406629/1_Nitro_2_phenylethane_the_main_constituent_of_the_essential_oil_of_Aniba_canelilla_elicits_a_vago_vagal_bradycardiac_and_depressor_reflex_in_normotensive_rats_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0014-2999(10)00290-6 DB - PRIME DP - Unbound Medicine ER -