phosphorus-radioisotopes has been researched along with Hypothyroidism* in 3 studies
2 review(s) available for phosphorus-radioisotopes and Hypothyroidism
Article | Year |
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Thyroidal regulation of renal energy metabolism and (Na+ + K+)-activated adenosine triphosphatase activity.
Topics: Adenosine Triphosphatases; Animals; Biological Transport; Body Temperature Regulation; Energy Metabolism; Hyperthyroidism; Hypothyroidism; Kidney; Kidney Cortex; Liver; Magnesium; Muscles; Oxygen Consumption; Phosphorus Radioisotopes; Potassium; Sodium; Thyroid Hormones; Thyroidectomy; Triiodothyronine | 1975 |
[Extracellular cyclic nucleotides: occurrence, analysis and diagnostic significance (author's transl)].
Topics: Chromatography, Ion Exchange; Cyclic AMP; Cyclic GMP; Diabetes Insipidus; Extracellular Space; Glucagon; Humans; Hyperthyroidism; Hypoparathyroidism; Hypothyroidism; Immune Sera; Inosine Nucleotides; Iodine Radioisotopes; Methods; Nucleotides, Cyclic; Phosphorus Radioisotopes; Protein Kinases; Tritium; Vasopressins | 1973 |
1 other study(ies) available for phosphorus-radioisotopes and Hypothyroidism
Article | Year |
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Age-related functional effects linked to phosphatase activity in ventricular myocytes.
Conflicting reports exist regarding the influence of beta-adrenergic stimulation on the maximum velocity of shortening (Vmax) in ventricular myocytes. This may be due to an unrecognized effect of maturation. In the present study, the effects of beta-adrenergic receptor stimulation on myocytes from hearts of juvenile nonbred and young adult retired breeder female rats were compared. Ventricular myocytes from young adults had a beta-adrenergic-dependent increase in Vmax and Ca2+-dependent actomyosin ATPase that was not observed in myocytes from juveniles. Myocytes from young adults had both an increase in beta-myosin heavy chain (MHC) and higher basal serine/threonine phosphatase activity compared with juvenile rats. Additional studies established moderate increases in beta-MHC induced by hypothyroidism do not confer myocardial beta-adrenergic responsiveness, whereas inhibition of the higher phosphatase activity in myocytes from young adults blocks the age-dependent, beta-adrenergic-induced increase in cross-bridge cycling rates. We propose that the higher phosphatase activity of myocytes from young adults compared with juveniles allows for a greater functional response of the myocardium to beta-adrenergic stimulation. Topics: Actin Cytoskeleton; Aging; Animals; Blotting, Western; Bucladesine; Calcium-Transporting ATPases; Enzyme Inhibitors; Female; Heart Ventricles; Hypothyroidism; In Vitro Techniques; Kinetics; Muscle Cells; Myocardial Contraction; Myocardium; Myofibrils; Myosin Heavy Chains; Okadaic Acid; Phosphates; Phosphoric Monoester Hydrolases; Phosphorus Radioisotopes; Phosphorylation; Rats | 2003 |