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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of medicinal chemistry 16 (1973), S. 700-703 
    ISSN: 1520-4804
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 7 (1969), S. 11-31 
    ISSN: 1432-1106
    Keywords: Cerebral Cortex ; Inhibition ; Ionic permeability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. In cats under Dial, thirty different anions were injected into some 400 cerebral cortical neurones, by diffusion from micro-electrodes, while observing IPSPs evoked by surface stimulation. 2. The probability of stable intracellular recording was much enhanced when micro-electrodes were filled with an organic salt of K. 3. With the exception of I03 −, all univalent anions tested were capable of producing a reversal of IPSPs in a substantial proportion of cases. IPSPs therefore appear to be associated with a high permeability to many univalent anions. 4. Apart from CrO4 −, multivalent anions only rarely caused a reversal of an IPSP. 5. The probability of observing a reversal with inorganic anions was a very steep function of their relative mobility in water. The relative mobilities through the membrane, calculated on the assumption that the membrane pores have the same permeability at rest and during IPSPs. are consistent with the hypothesis that inorganic anions travel through pores whose equivalent diameter is about twice the diameter of hydrated Cl− and is appreciably greater than that of the corresponding pores in spinal motoneurones. 6. The probability of observing a reversal with organic univalent anions (mainly of aliphatic and aromatic acids) bore an approximately linear relation to their mobility in water. These anions have a much higher mobility through the membrane (during inhibition, and perhaps even at rest) than would be expected from their size if they travel through the same pores as the inorganic anions. 7. As in other membranes, the rate of diffusion of various ions is evidently determined not only by the ions' size relative to membrane pores, but also by their chemical structure and their ability to interact with membrane constituents.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 81 (1983), S. 28-32 
    ISSN: 1432-2072
    Keywords: Opiate-induced feeding ; Opiate-induced drinking ; Species differences ; Rats ; Hamsters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The proposed μ and ϰ opiate receptor agonists morphine and ketocyclazocine, as well as meperidine, were compared for their ability to stimulate feeding and drinking by male rats and hamsters that were not deprived of food or water. Morphine (8.0 mg/kg) and ketocyclazocine (0.5–4.0 mg/kg), but not meperidine (0.5–64.0 mg/kg), increased 3-h food intake by rats. By 6 h the hyperphagic responses were less pronounced. However, 6-h water intake was increased by all three agonists. In contrast to rats, hamsters failed to increased food or water intake over an 8-h period following morphine (6.25–800 mg/kg), ketocyclazocine (0.25–16.0 mg/kg), or meperidine (1.0–128 mg/kg) administration. Thus, ϰ or μ opiate receptors may mediate the observed hyperphagic effect of opiate agonists on rat food intake. In addition, these results are consistent with our earlier suggestion that hamsters lack an opiate-sensitive feeding system.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0738
    Keywords: Key words: Cyanide – K+ channels – Hyperpolarization – bis-Oxonol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Exposure of rat pheochromocytoma (PC12) cells to cyanide produces elevation of cytosolic calcium, impaired Na+-H+ exchange, membrane lipid peroxidation and release of neurotransmitters. Since these observations suggested cyanide alters plasma membrane function, the present study examined the effect of NaCN on the membrane potential of undifferentiated PC12 cells in suspension. In PC12 cells loaded with the voltage sensitive fluorescent dye, bis-oxonol, cyanide (2.5 – 10 mM) elicited an immediate (within seconds), concentration related decrease in fluorescence, indicating hyperpolarization of the plasma membrane. Increasing extracellular K+ concentration to 20 mM blocked the effect of cyanide (5 mM), suggesting cyanide increased K+ efflux. Pretreatment with quinine blocked the cyanide-induced hyperpolarization, whereas glyburide had little effect, showing the hyperpolarization produced by cyanide was due to activation of Ca2+ sensitive K+ channels. Removal of Ca2+ from the media did not influence cyanide-induced hyperpolarization. However, buffering intracellular Ca2+ by loading cells with the Ca2+ chelators, Quin II or BAPTA, abolished the cyanide effect, showing cytosolic Ca2+ is a key factor. These findings suggest that cyanide mobilizes Ca2+ from intracellular stores which leads to hyperpolarization via the activation of Ca2+ sensitive K+ channels.
    Type of Medium: Electronic Resource
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