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R Deth

Publications and source records attributed to R Deth.

6 recordsLinked to original sources

Inhibition of alpha-receptor-induced Ca2+ release and Ca2+ influx by Mn2+ and La3+.

The influence of Mn2+ and La3+ on alpha-receptor-stimulated Ca2+ movements was examined in arterial smooth muscle of the rabbit aorta. Both cations cause an inhibition of phenylephrine (PE) contractile response which exhibits a different pattern at low and high cation concentrations. At 0.1-1.0 mM inhibition by Mn2+ and La3+ was predominately due to a reduction in Ca2+ influx reflected as inhibition of the slow phase of contraction and reduction in PE-stimulated 45Ca uptake. PE log dose-response curves were shifted to the right in a non-parallel manner by 1 mM Mn2+ such that responses to lower PE concentrations were more inhibited. However, in the presence of 10 mM Mn2+ PE responses are equally inhibited at all PE levels. At 10 mM both Mn2+ and La3+ also inhibited PE-stimulated Ca2+ release resulting in a reduction in both the rapid phase of contraction and in the magnitude of PE stimulation of 45Ca efflux. The effects of Nm2+ (1 or 10 mM) on contraction and 45Ca efflux were rapidly reversible, while the effect of La3+ was not. Inhibition of Ca2+ release by 10 mM Mn2+ and La3+ was not caused by displacement of releasable Ca2+, but appeared to reflect their occupation of a superficially located receptor modulating site. The inhibition of Ca2+ influx by lower concentrations of Mn2+ may illustrate the functional consequence of configurational changes in the alpha 2-form of the receptor which have been recently described at lower concentrations of divalent cations.

Animals↗

Agonist induced release of intracellular Ca2+ in the rabbit aorta.

The effects of hormonal agonists (norepinephrine, angiotensin, and histamine) on 45Ca efflux from the rabbit aorta were studied using a Ca-EGTA buffered efflux medium. Each caused a transient stimulation of efflux rate which probably reflected the release of an intracellular 45Ca store. The size of the stimulation of efflux correlated with the size of the initial rapid phase of contraction. The norepinephrine-sensitive intracellular Ca fraction was estimated to be greater than 21 mumoles/Kg wet tissue weight. This fraction is separate from intracellular Ca which is accumulated during relaxation. Evidence is presented for the lack of cyclic nucleotide involvement in the release of Ca2+, and possible alternative modes of coupling are discussed.

Angiotensin II↗

A study of releasable Ca fractions in smooth muscle cells of the rabbit aorta.

The distribution of Ca in the cellular compartment of smooth muscle cells of the rabbit aorta has been studied by analyzing the effect of norepinephrine, caffeine, and DNP on 45Ca exchange and on the pattern of tension development. These three substances increase the release of 45Ca from the tissue, but DNP acts more slowly than norepinephrine or caffeine. Also, the effect of norepinephrine and caffeine on tension development occurs almost immediately, while that of DNP appears only after a delay of 5 min. Study of the effect of these substances on the Ca efflux has shown that norepinephrine and caffeine act probably on the same Ca compartment, while DNP seems to act on a different compartment with a slower exchange rate. The difference between these two pools could be further demonstrated by studying Ca release after loading the tissues with tracer in either K-rich solution or in a solution with reduced [Ca]o. The K depolarization results in an excessive loading of the cells with 45Ca. Exposing these cells during the efflux procedure to a solution containing DNP causes a much larger release of 45Ca than that observed after a loading procedure in normal solution. In contrast, the release of 45Ca elicited in such tissues by norepinephrine or caffeine disappears. This disappearance is due to the prolonged increase of the Ca exchangeability induced by K depolarization. During initial exposure to PSS the increased exchangeability causes an accelerated loss of tracer from the tissue compartment on which norepinephrine and caffeine act, while the DNP sensitive compartment is not affected. It is suggested that noradrenaline and caffeine act on the same calcium pool close to the membrane and that DNP acts mainly on the mitochondria.

Animals↗

Effects of nisoldipine, a new calcium antagonist, on myocardial infarct size and cardiac dynamics following acute myocardial infarction.

While some calcium antagonists are effective in reducing myocardial infarct size, this beneficial effect may be accompanied by negative inotropic effects. In the following study, a new dihydropyridine calcium antagonist, nisoldipine, was assessed for its effect on infarct size, hemodynamics, and regional function as assessed by percent systolic wall thickening of the left ventricle (SWT) by 2D echocardiography. Open-chest, anesthetized dogs were subjected to 6 h of coronary artery occlusion. After 10 min of coronary artery occlusion, the ischemic area at risk of infarction (AR; % of left ventricle) was determined by left atrial injection of 99mTc-labeled albumin microspheres with subsequent postmortem autoradiography. After 6 h, the hearts were excised, and the area of necrosis (AN) determined by incubation of left ventricular slices in triphenyltetrazolium chloride stain. Treated dogs received 0.005 mg/kg nisoldipine by intravenous infusion at 1.91 ml/min (lasting approximately 8.7 min) during three dosing periods: 15 min, 2 h, and 4 h postocclusion. The AR of eight controls (25.7 +/- 1.8%) was not significantly different from that of 11 treated dogs (25.1 +/- 1.9%). However, the AN/AR X 100 of treated dogs was significantly less than that of controls (62.8 +/- 9.3 vs. 91.6 +/- 7.0%; p less than 0.05). Mean arterial pressure fell in treated dogs by 15.7% (p less than 0.01) at 15 min and by 5.7% (p less than 0.05) at 4 h but not at 2 h postocclusion. Heart rate was not affected by nisoldipine.(ABSTRACT TRUNCATED AT 250 WORDS)

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