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Biomedical subjects

W G Sanborn

Publications and source records attributed to W G Sanborn.

10 recordsLinked to original sources

Parathyroid hormone has a positive inotropic action in the rat.

Parathyroid hormone (PTH: synthetic bovine, amino terminus 1-34 amino acids) demonstrates a positive inotropic action on the isolated papillary muscle of the rat heart. The effect was evident at PTH concentration of 10(-12)M, and the maximum inotropic effect occurred with PTH concentrations greater than 10(-11)M. Biologically inactive PTH (PTH treated with H2O2) was without effect. The inotropic effect of PTH was partially blocked by propranolol and also suppressed in the papillary muscle of the rat pretreated with reserpine. Methoxyverapamil completely blocked the inotropic action of PTH. PTH was without effects on adenylate cyclase activity of the myocardium. Results show the presence of an inotropic action of PTH in vitro and suggest that this action of PTH is partially mediated by releasing the endogenous myocardial norepinephrine which exerts a positive inotropic effect via beta-adrenergic stimulation and by an increase in Ca++ influx across plasma membranes, but independent of adenylate cyclase activation. The inotropic action of PTH may be of significance in normal cardiac function.

Animals↗

High-resolution radioisotopic measurements of calcium, strontium, and barium in heart.

A gamma-ray detector system used in conjunction with isolated vascularly perfused rabbit septa labeled with the Ca-like cations 85Sr and 133Ba has been developed to test the feasibility of constructing a considerably more efficient detector system capable of measuring the highly energetic (Emax congruent to 1.3 MeV) 47Ca radionuclide. In addition an experimental design has been developed to quantify, statistically, perturbations of total tissue Ca, Sr, or Ba should they occur. This project was undertaken because the severe attenuation by living tissue of the beta-emitting radionuclide 45Ca (Emax congruent to 250 keV) limits its usefulness as a Ca tracer during experiments in which total tissue Ca is being measured minute-by-minute by an external detector. Analyses of over 100 experiments conducted on 35Sr- and 133Ba-labeled rabbit septa indicate that a tissue-detector system can be developed having the capacity to resolve perturbations of as little as 2 mumol Ca/kg wet tissue at 1-min sampling times or 6 mumol Ca/kg wet tissue at 0.1-min sampling times.

Animals↗

Specific uncoupling of excitation and contraction in mammalian cardiac tissue by lanthanum.

Arterially cannulated rabbit interventricular septal tissue was exposed to 5-40 microM La in 2.5 mM Ca perfusate. Immediately following perfusion with La two concurrent events were consistently observed: (a) a rapid decline of active tension to a lesser steady-state value, and (b) an abrupt, release of short duration of tissue-bound Ca. The magnitude of both events was directly related to the [La](o). If the duration of exposure to La was brief, contractility returned toward normal upon return to the La-free perfusate. Elevation of [Ca](o) during exposure to La counteracted its effect and induced a concurrent displacement of tissue-bound La. Cellular action potentials recorded during brief perfusion with La demonstrated that essentially normal regenerative depolarization was maintained. Analysis of the quantities of (45)Ca released following exposure to 10 microM La indicated that this La-susceptible Ca was being displaced from a homogeneous pool-the one previously shown by Langer to represent contractile dependent Ca. These data led to the following conclusions: During perfusion with 2.5 mM Ca contractile dependent Ca was derived primarily from "superficially" located sites. La effected the release of contractile dependent Ca by modifying the normal permselectivity of this "superficial" membrane for activator Ca. These and other data infer that contractile dependent Ca is derived primarily from superficially located sites.

Action Potentials↗