about
Increased circulating vasopressin may account for ethanol-induced hypertension in ratsEthanol consumption increases blood pressure and alters the responsiveness of the mesenteric vasculature in ratsBoth α1- and α2-adrenoceptors in the insular cortex are involved in the cardiovascular responses to acute restraint stress in rats.Acute reversible inactivation of the bed nucleus of stria terminalis induces antidepressant-like effect in the rat forced swimming test.Dorsal and ventral hippocampus modulate autonomic responses but not behavioral consequences associated to acute restraint stress in rats.Involvement of the medial prefrontal cortex in central cardiovascular modulation in the rat.Increased endothelin-1 reactivity and endothelial dysfunction in carotid arteries from rats with hyperhomocysteinemia.Angiotensin II binding sites in the anteroventral-third ventricle (AV3V) area and related structures of the rat brain.High histamine levels in specific hypothalamic nuclei of Brattleboro rats lacking vasopressin.Brain sites involved in the antinociceptive effect of bradykinin in rats.Fluorescent probes of alpha- and beta-adrenergic and opiate receptors: biochemical and histochemical evaluation.The bed nucleus of the stria terminalis modulates exercise-evoked cardiovascular responses in rats.Paraventricular nucleus modulates autonomic and neuroendocrine responses to acute restraint stress in rats.Both alpha1 and alpha2-adrenoceptors mediate the cardiovascular responses to noradrenaline microinjected into the bed nucleus of the stria terminal of rats.Cardiovascular responses to L-glutamate microinjection into the hypothalamic paraventricular nucleus are mediated by a local nitric oxide-guanylate cyclase mechanism.N-methyl-D-aspartate glutamate receptors in the hypothalamic paraventricular nucleus modulate cardiac component of the baroreflex in unanesthetized rats.alpha(1)-Adrenoceptors in the lateral septal area modulate food intake behaviour in rats.The medial forebrain bundle mediates cardiovascular responses to electrical stimulation of the medial prefrontal cortex.Effect of NMDA-induced lesion of the subfornical organ on the angiotensin II binding sites density and acetylcholinesterase or NADPH-diphorase activities in the lamina terminalis of the rat brain.Mechanism of the cardiovascular responses caused by L-proline microinjected into the supraoptic nucleus of the hypothalamus in unanesthetized rats.N-methyl-D-aspartate receptors in the insular cortex modulate baroreflex in unanesthetized rats.Mechanisms involved in the water intake-related pressor response in the rat.Structural and functional characterization of an acidic platelet aggregation inhibitor and hypotensive phospholipase A(2) from Bothrops jararacussu snake venom.Mechanisms involved in the pressor response to noradrenaline injection into the cingulate cortex of unanesthetized rats.Perivascular injury leads to a reduction in vascular reactivity of the collared and to an enhancement on contralateral carotid artery of rats.Time-course of neuroendocrine changes and its correlation with hypertension induced by ethanol consumption.Involvement of dorsal hippocampus glutamatergic and nitrergic neurotransmission in autonomic responses evoked by acute restraint stress in rats.Cardiovascular responses to glutamate microinjection in the dorsomedial periaqueductal gray of unanesthetized rats.Paraventricular nucleus mediates pressor response to noradrenaline injection into the dorsal periaqueductal gray area.The diagonal band of Broca is involved in the pressor pathway activated by noradrenaline microinjected into the periaqueductal gray area of rats.Role of paraventricular nucleus in exercise training-induced autonomic modulation in conscious rats.Bed nucleus of the stria terminalis N-methyl-D-aspartate receptors and nitric oxide modulate the baroreflex cardiac component in unanesthetized rats.Mechanisms involved in the pressor response to noradrenaline microinjection into the supraoptic nucleus of unanesthetized rats.Diagonal band of Broca modulates the cardiac component of the baroreflex in unanesthetized rats.Pressor and tachycardic responses evoked by microinjections of L-glutamate into the medial prefrontal cortex of unanaesthetized rats.Mechanisms underlying the biphasic effect of vitamin K1 (phylloquinone) on arterial blood pressure.Non-N-methyl-D-aspartate glutamate receptors in the paraventricular nucleus of hypothalamus mediate the pressor response evoked by noradrenaline microinjected into the lateral septal area in rats.The lateral septal area is involved in the pressor pathway activated by microinjection of norepinephrine into the rat brain cingulate cortex.Activation of CB1 cannabinoid receptors in the dorsolateral periaqueductal gray reduces the expression of contextual fear conditioning in rats.Neural connections between prosencephalic structures involved in vasopressin release.
P50
Q28569885-70D04D82-745A-4BB8-8798-B38B089D88F0Q28571631-48DD9780-B344-41E4-AB05-A1E311C0D514Q30444671-A0F297B8-3B8B-44FC-9369-75D7F23FEA57Q33921512-D70B4DA0-9DE1-421F-840B-3491E15BE900Q35023383-C64AD727-3853-4B5E-AF69-06268AF3E7B1Q36444156-9073FA9E-E399-422A-B03B-932E9F3BAC6DQ37255301-DD543D2A-D17A-4D6A-8FBD-9A15947DCECEQ41366761-E118A37D-2649-47D6-AE20-B612B254E9D9Q41587766-76308164-464B-4D82-AAD5-4F5A3B073680Q41887929-7FF18623-B370-4689-8EB4-2A397066548EQ42241865-877BFD87-FBBE-4DD9-BFCD-B521BE555939Q42632257-B4F88590-DA40-4E5D-A97D-AFB09EE498BCQ42994882-2B0AD48A-319A-4721-90FC-14C929C74F19Q43042656-8547E4E5-37C4-492E-B384-0D2FD39DEFFFQ43061376-2E51FBEA-F096-4E40-8997-195C0BFF127BQ43062547-7F6F8996-E2BC-4296-90A0-D5D3BA6FCF22Q43241591-20D0C14E-6236-4F59-B2B1-FC0F1D14AAFBQ43434198-CAB25777-93EC-4514-A2EE-4B51859CD7CCQ43663983-4E9B064A-DB30-483A-A9DC-F5EA570E40C3Q43708789-6F14B47C-883D-47E0-9610-F334EEC0E72DQ43787517-38824A3B-2511-4308-BCEF-73696338C77FQ43872944-9A16A0D5-B911-4077-B2AD-37362C97771FQ44094218-CAF51093-064B-4C86-925C-0D388171CD9FQ44394163-C90DAF02-52E0-4EDB-B614-1F3FE059078BQ45052452-9816792F-3602-4EDF-B183-82D895504E2FQ45175552-11C30437-7BA9-4FBF-832E-9D9A3B6660F8Q45410857-1F250FD3-88BF-43F9-84D9-F704586FD4DFQ45897125-E944D202-CBF3-4899-BD97-42990ABC5C97Q45947577-3DA8D1F4-D57B-4A18-9EEF-4BBC5358BFDEQ46080360-1432A302-3AD3-4160-807E-2002976A1567Q46083260-59C5F3A6-BA0E-49EF-A52F-1B0015755DCFQ46155000-4792F00C-9C32-4D4B-A7C1-132BE23574C3Q46212675-B72ED21E-D326-4051-B279-84C5E7E670CAQ46292050-22E1DF71-4A2E-4B03-A48B-51E07C424AC8Q46524835-41A52C5C-CF28-4503-888A-F338406E152FQ46543646-ED71E8FA-85C6-4E85-B47F-0473D8E7D903Q46548566-FE942B95-06A2-446E-9E66-25E60516CD50Q46553307-F470902E-7F85-4E1C-8C52-5B088ADA5E42Q46619355-5E279A0F-93C7-4259-8940-8B9BB60814ADQ46630915-16C30F03-6674-46C1-BBCC-7E72F2E84C04
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Fernando Morgan Aguiar Correa
@ast
Fernando Morgan Aguiar Correa
@en
Fernando Morgan Aguiar Correa
@es
Fernando Morgan Aguiar Correa
@nl
Fernando Morgan Aguiar Correa
@sl
type
label
Fernando Morgan Aguiar Correa
@ast
Fernando Morgan Aguiar Correa
@en
Fernando Morgan Aguiar Correa
@es
Fernando Morgan Aguiar Correa
@nl
Fernando Morgan Aguiar Correa
@sl
prefLabel
Fernando Morgan Aguiar Correa
@ast
Fernando Morgan Aguiar Correa
@en
Fernando Morgan Aguiar Correa
@es
Fernando Morgan Aguiar Correa
@nl
Fernando Morgan Aguiar Correa
@sl
P1053
D-1614-2012
P106
P21
P2798
P31
P3829
P496
0000-0003-4067-9524