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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 21 (1974), S. 229-240 
    ISSN: 1432-1106
    Keywords: Visual system ; Pigeon ; Thalamus ; Evoked potential ; Cryogenic blockade
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In 4 dorsolateral thalamic nuclei (LA, DLAmc, DLLd and DLLv) short latency evoked responses were recorded after electrical or photic stimulation of the contralateral eye. Electrical stimulation of these 4 nuclei led to bilaterally evoked responses in the wulst, where previous experiments had demonstrated an oligosynaptic projection from the retina. Cooling in DLL, while stimulating the contralateral optic nerve, leads to a severe decrement of both wulst responses suggesting that the thalamus functions as a relay within the retino-thalamo-hyperstriatal pathway. When the optic nerve ipsilateral to the cooled thalamus is stimulated the ipsilateral wulst response is unchanged while the contralateral wulst response is enhanced, suggesting a disinhibition. Similarly an inhibitory effect of the thalamus on one side upon the contralateral wulst response was found after concomitant stimulation of one optic nerve and a delayed stimulation of the ipsilateral thalamus. The dorsolateral thalamic group is the origin of bilateral wulst projections, the pathway to the contralateral telencephalon was demonstrated to pass via the supraoptic decussation DSO. Cooling DSO diminished the inhibitory thalamic effect upon the contralateral wulst. DSO was corroborated as part of the ipsilateral retino-wulst system.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 27 (1984), S. 589-593 
    ISSN: 1432-1041
    Keywords: piretanide ; renal insufficiency ; furosemide ; pharmacokinetics ; loop diuretic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of piretanide was studied in 10 patients with chronic renal failure. After administration of a high oral dose (12 to 192 mg) of piretanide the kinetics behaved according to an open 2-compartment model. The elimination constant in the first phase (α) ranged from 0.385 to 0.756 h−1 and in the second phase (β) from 0.079 to 0.274 h−1. The corresponding elimination half-lives ranged from 55 to 108 min (t1/2 α) and from 152 to 524 min (t1/2 β). Only an average of 2.8% of the orally administered drug was recovered in 24 h urines. Nevertheless, a good correlation was found between urinary recovery or renal clearance of the drug and residual renal function. The elimination of piretanide by non-renal mechanisms appeared to be increased when renal function was greatly diminished.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1912
    Keywords: HOE 498 ; Angiotensin converting enzyme inhibition ; Angiotensin II
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The converting enzyme inhibitor HOE 498 was evaluated in 12 normotensive male volunteers aged 21 to 26. The efficacy of single 5, 10 or 20 mg oral doses in blocking the pressor response to exogenous angiotensin I was tested in 3 of the subjects. All 3 doses of HOE 498 reduced the pressor response to exogenous angiotensin I to below 50% of control within 1,5 h following administration of the drug. Plasma renin and converting enzyme activity, blood angiotensin I, as well as plasma angiotensin II and aldosterone were measured serially before and up to 72 h following oral administration of a single dose of 2.5, 5, 10 or 20 mg of HOE 498 to groups of 5 volunteers each. As expected, blood angiotensin I levels and plasma renin activity rose while plasma converting enzyme activity, plasma angiotensin II and aldosterone concentration fell after administration of the drug. While the dose of 2.5 mg did not reduce plasma converting enzyme activity below 20% of control, the higher doses all resulted in plasma converting enzyme inhibition exceeding 90%. No side-effects were observed. It is concluded that in normal volunteers HOE 498 is an effective potent and long-acting converting enzyme inhibitor. Based on these preliminary findings it is expected that 5 mg HOE 948 will turn out to be adequate for therapeutic use.
    Type of Medium: Electronic Resource
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