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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical and experimental pharmacology and physiology 16 (1989), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 1. The effects of the calcium channel blocker, ω-conotoxin, on sympathetic neuroeffector function in the guinea-pig vas deferens have been investigated using a combination of mechanical and electrophysiological recording techniques.2. Diphasic contractions evoked by electrical field stimulation were irreversibly abolished by ω-conotoxin (10–100 nmol/L).3. Electrically evoked excitatory junction potentials and currents were irreversibly blocked by ω-conotoxin (10–100 nmol/L). Spontaneous excitatory junction potentials and currents were unaffected by this treatment.4. ω-Conotoxin did not block impulse propagation in the nerve terminals. However, in three of four experiments ω-conotoxin caused a decrease in the size of the nerve terminal impulse.5. These findings support the suggestion the co-conotoxin acts prejunctionally to inhibit sympathetic neuroeffector by interfering with depolarization-secretion coupling.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] In rat and guinea pig, the contractile response of the vas def erens to a single field stimulus to the sympathetic innervation consisted of several components. In the rat this response could be separated into two components; a rapid, early (200-300 ms) response (/s) and a slower (600-700 ms) ...
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1912
    Keywords: Guinea-pig vas deferens ; Sympathetic nerves ; Electrophysiology ; α2-Autoinhibition ; Yohimbine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Excitatory junction potentials (e j.ps; intracellular electrodes) and excitatory junction currents (e.j.cs; extracellular electrodes) elicited by stimulation (20 pulses at 1 Hz every minute) of the hypogastric nerve trunk were recorded from guinea-pig isolated vas deferens. Intracellular recording. At a variety of stimulation intensities, bath-applied yohimbine (0.1–1 μmol/l) did not change the first one to three e j.ps in a train but increased the amplitude of subsequent e j.ps. The effect of yohimbine was abolished in tissues from reserpinepretreated guinea pigs. Bath-applied desipramine (0.1 μmol/l) diminished the amplitude of all but the first one to three e j.ps in a train. - Extracellular recording. Yohimbine (0.1–1 μmol/l), when applied locally through the recording suction electrode, increased the number of e.j.cs per given number of stimuli, i. e., enhanced the probability of occurrence of e.j.cs. When desipramine (0.1 μmol/l) was present both in the bath and in the recording electrode, the probability of the occurrence of e.j.cs was decreased. In the presence of desipramine, yohimbine (0.1–1 μmol/l) increased the number of e j.cs even more markedly. Neither the nerve terminal impulse nor the number of spontaneous e j.cs was changed by yohimbine. A mixture of tetraethylammonium (2 mmol/l) and 4-aminopyridine (0.2 mmol/l), when applied locally, both increased the number of e.j.cs and changed markedly the shape of the nerve terminal impulse. These experiments demonstrate presynaptic α2-autoinhibition at a high degree of resolution, i. e., when the intermittent release of transmitter from only a few varicosities along a single terminal axon is monitored by the e j.c. α2-Autoinhibition is not due to a depression of impulse conduction but to a depression of stimulus-secretion coupling in varicosities reached by the impulse. Taken together with the low probability of transmitter release at the level of individual varicosities, the results support the idea of lateral inhibition by noradrenaline released from distant varicosities rather than inhibition due to noradrenaline released from the same varicosity. The mode of action of yohimbine differs from that of K+ channel blocking agents.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 345 (1992), S. 424-430 
    ISSN: 1432-1912
    Keywords: Rabbit jejunal artery ; Contraction ; Cotransmission ; ATP ; Noradrenaline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Isotonic contractions of the rabbit jejunal artery were evoked by perivascular nerve stimulation with trains of 10 or 100 stimuli at 2 Hz or 10 Hz. Short trains of stimuli elicited contractions that were totally resistant to α-adrenoceptor blockade (0.1 μmol/l prazosin) but blocked by α,β-methylene ATP (1 μmol/l). A substantial noradrenergic component of contraction comprising about 50% of the total could be evoked by adjusting the stimulation parameters (increasing the frequency and/or number of stimuli in a train). The noradrenergic and the purinergic components are derived from sympathetic nerves as both were blocked by TTX and the adrenergic neurone blocker guanethidine (3 μmol/l). It is concluded that the contraction of the rabbit jejunal artery to short trains of stimuli is predominantly purinergic, a nor-adrenergic component only being revealed at higher frequencies of stimulation or during longer trains of stimuli. The purinergic component of contraction is derived from sympathetic nerves and not from a separate population of purinergic nerves.
    Type of Medium: Electronic Resource
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