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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical and experimental pharmacology and physiology 11 (1984), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 1. Urapidil had blocking activity on α1-adrenoceptors in the rat isolated caudal artery (pA2≏ 7) and in the anaesthetized rat.2. Urapidil had no clonidine like agonistic activity on α2-adrenoceptors in preparations of the guinea-pig ileum (prejunctional) or dog saphenous vein (postjunctional).3. Urapidil (0.01–0.1 mg/kg i.v.) had a hypotensive effect in the anaesthetized rat. In a dose of 0.1 mg/kg, the depressor response was accompanied by bradycardia. Vagotomy abolished the bradycardia and attenuated the depressor response.4. The results indicate that the antihypertensive effect of urapidil may be due partly to blockade of postjunctional α1-adrenoceptors, but in addition there is a central component of action.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Cardiopulmonary vagal reflex ; Bezold-Jarisch reflex ; Excitatory amino acid ; Caudal ventrolateral medulla ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The importance of the caudal ventrolateral medulla (CVLM) in mediating vagal cardiopulmonary (Bezold-Jarisch reflex) reflex activity was studied in urethane-anaesthetized rats. Unilateral electrolytic lesion of the CVLM markedly attenuated Bezold-Jarisch reflex responses (hypotension and bradycardia) elicited by intravenous injections of 5-HT. Bilateral lesion of the CVLM virtually abolished the reflex responses. Microinjection of the excitatory amino acid (EAA) receptor antagonist kynurenate (KYN), but not the inactive analogue xanthurenate, into the CVLM markedly attenuated the reflex responses to 5-HT. The N-methyl-D-aspartate (NMDA) receptor antagonist, MK-801 also markedly attenuated reflex activity. Furthermore, lesions, KYN and MK-801 all tended to elevate resting blood pressure and to reduce resting heart rate. These findings support the hypothesis that the CVLM is an important medullary locus mediating cardiovascular reflex integration and that an EAA synapse in the CVLM is important in the cardiopulmonary reflex arc.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2072
    Keywords: Δ9-Tetrahydrocannabinol ; Clomipramine ; Withdrawal-like behaviour
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Rats chronically treated with increasing daily doses of Δ9-tetrahydrocannabinol (Δ9-THC) for up to 5 or 10 days exhibit a withdrawal-like behavioural response when challenged with clomipramine, a potent inhibitor of serotonin (5-hydroxytryptamine) reuptake, at the time when the next injection of Δ9-THC was due. To determine whether this response is indeed a withdrawal syndrome, different groups of rats were injected IV twice daily for up to 5 days with either Δ9-THC, in doses increasing from 2–6 mg/kg, or polyvinyl-pyrrolidone (PVP), the vehicle in which Δ9-THC was suspended. On day 6, an acute dose of 6 mg/kg Δ9-THC was given 30 min before IP clomipramine (15 mg/kg). The total behavioural response, which included writhing, backward kicking, jumping, head shaking, and paw tremor, was attenuated in rats chronically treated with Δ9-THC, but not in rats which received an acute dose of PVP. These results lend further evidence to our hypothesis that chronically administered Δ9-THC produces a state of physical dependence in the rat.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2072
    Keywords: Δ 9-Tetrahydrocannabinol ; Withdrawal-like behaviour ; Body weight ; Food consumption ; Imipramine ; Clomipramine ; Fluoxetine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of the biogenic amine reuptake inhibitors fluoxetine, clomipramine and imipramine on the behaviour of rats after chronic treatment with Δ 9 tetrahydrocannabinol (Δ 9-THC) for 5 and 10 days were examined. Rats with permanently in-dwelling IV cannulae were injected twice daily with doses of Δ 9-THC (2–6 mg/kg). Δ 9-THC treatment reduced the rate of body weight gain and induced the typical biphasic modifications of behaviour. Tolerance developed to both of these effects. On days 6 and 11 of the experiment, rats were injected IP with 15 mg/kg imipramine HCl, clomipramine HCl or fluoxetine HCl, and behaviour, consisting of writhes, backward kicks, jumps and wet shakes, was observed for the next 30 min. Each of the amine reuptake inhibitors induced changes in behaviour, the severity of which appeared to correlate with their ability to inhibit the reuptake of 5-hydroxytryptamine (5-HT). It is suggested that tryptaminergic mechanisms are involved in the production of a withdrawal-like behaviour after chronic Δ 9-THC treatment.
    Type of Medium: Electronic Resource
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