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Bi-directional cb1 receptor-mediated cardiovascular effects of cannabinoids in anaesthetized rats: Role of the paraventricular nucleus
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نویسنده
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grzeda e. ,schlicker e. ,luczaj w. ,harasim e. ,baranowska-kuczko m. ,malinowska b.
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منبع
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journal of physiology and pharmacology - 2015 - دوره : 66 - شماره : 3 - صفحه:343 -353
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چکیده
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The activation of cannabinoid cb1 receptors decreases and increases blood pressure (bp) in anaesthetized and conscious rats,respectively. the aim of our study was to check the possible involvement of cb1 receptors in the paraventricular nucleus of the hypothalamus (pvn) in the cardiovascular effects of cannabinoids in rats. methanandamide (metabolically stable analogue of the endocannabinoid anandamide) and the synthetic cannabinoid receptor agonist cp55940 were microinjected into the pvn of urethane-anaesthetized rats twice (s1 and s2,20 min apart). receptor antagonists were administered intravenously (i.v.) 5 min before s2. methanandamide and cp55940 decreased blood pressure by 15 – 20%. the cb1 receptor antagonist am251 reversed the depressor effect into a pressor response of 20 – 30%. the pressor effect of cp55940 observed in the presence of am251 i.v. was reduced by am251 given additionally into the pvn but not by the i.v. injection of the cb2 antagonist sr144528 or the vanilloid trpv1 antagonist ruthenium red. in the presence of the peripherally restricted cb1 receptor antagonist am6545,cp55940 given into the pvn increased bp by 40%. am6545 reversed the decrease in bp induced by cp55940 i.v. into a marked increase. bilateral chemical lesion of the pvn by kainic acid abolished all cardiovascular effects of cp55940 i.v. in conclusion,the cannabinoid cp55940 administered to the pvn of urethane-anaesthetized rats can induce depressor and pressor effects. the direction of the response probably depends on the sympathetic tone. the centrally induced hypertensive response of cp55940 can,in addition,be masked by peripheral cb1 receptors.
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کلیدواژه
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Anandamide; Cannabinoid receptor; Cannabinoids receptor antagonists; Cardiovascular effects; Haemodynamic responses; Hypothalamus; Methanandamide; Paraventricular nucleus
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آدرس
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department of experimental physiology and pathophysiology,medical university of bialystok,bialystok, Poland, department of pharmacology and toxicology,university of bonn,bonn, Germany, department of inorganic and analytical chemistry,medical university of bialystok,bialystok, Poland, department of physiology,medical university of bialystok,bialystok, Poland, department of experimental physiology and pathophysiology,medical university of bialystok,bialystok, Poland, department of experimental physiology and pathophysiology,medical university of bialystok,bialystok, Poland
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Authors
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