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K D Straub

Publications and source records attributed to K D Straub.

46 records · Page 3Linked to original sources
PubMed1969

ADP kinase and ATPase in chloroplasts.

Treatment of chloroplasts with trypsin activates a light-requiring ATPase whose properties are strikingly similar to those of the light-requiring ADP kinase of chloroplasts. The observations here presented suggest that there exists, in chloroplasts, a reducible enzyme which, in its reduced state, catalyzes the reversible reaction: P(i) (-2) + ADP(-3) + H(+) right harpoon over left harpoon ATP(-4) + H(2)O. By reduction and protonation of the catalytic site of this enzyme, light-driven electron flow in the chloroplast drives the reaction to the right. Hydrolysis of ATP proceeds only when the enzyme is reduced and when the proton concentration within the chloroplast is kept at low levels, viz., in the absence of light, in the presence of uncoupling agents which decrease the concentration of internal H(+), or in the presence of electron acceptors which by oxidizing the internal electron acceptors also decrease the proton potential. Activation of the enzyme requires light; it remains active only in the presence of ATP. Hydrolysis of all the ATP results in inactivation of the ATPase. The membrane-bound protein CF(2) limits the reversibility of the reaction by excluding ATP and H(2)O from the enzyme site. It also facilitates the ability of the chloroplasts to accumulate and to maintain high internal concentrations of such ions as ADP, P(i), PMS(+), and imidazole.

Adenosine Triphosphatases↗
PubMedDate not supplied

Alteration in calcium metabolism in mitochondria isolated from ischemic and reperfused myocardium.

This study determines the effect of ischemia and reperfusion on energy-linked Ca2+ uptake by myocardial mitochondria. The left anterior descending coronary artery was occluded in 14 mature pigs for 2 hr. In seven animals the ligature was released and the ischemic zone reperfused for 2 additional hours. After sacrifice, mitochondrial function was measured in normal and reperfused or ischemic areas of the left ventricle, using a polarographic method. Mitochondria were prepared without EDTA by standard procedures and Ca2+ uptake measured by 45Ca2+ isotope tracer. Uptake of Ca2+ by mitochondria derived from ischemic myocardium is markedly impaired with or without phosphate. Reperfusion may accentuate this impairment. The presence of exogenous Ca2+ inhibits the ability of ischemic or reperfused mitochondria to phosphorylate ADP.

Animals↗
PubMedDate not supplied

Digitalis-sensitive Na+, K+-ATPase: lack of a direct catecholamine-mediated stimulation in bovine myocardial tissue.

It has been documented that biogenic amines can stimulate Na+, K+-ATPase from various tissue preparations. However, it is unclear whether or not this stimulation occurs in myocardial tissues. We have evaluated possible catecholamine stimulation of purified Na+, K+- ATPase preparations utilizing a bovine ventricular microsomal preparation. We have studied the dose response of the enzyme to ouabain and digitoxigenin in the presence and absence of propranolol and norepinephrine. Our results indicate that propranolol increases the sensitivity of Na+, K+-ATPase to inhibition by digitalis, and that stimulation of Na+, K+-ATPase in bovine myocardium is not mediated via an adrenergic mechanism. In addition, our results indicate that in myocardial tissue, both stereoisomers of propranolol produce a direct nonspecific membrane effect which can modify Na+, K+-ATPase activity.

Animals↗
PubMedDate not supplied

Alterations of membrane potential and Ca2+ flux of sarcoplasmic reticulum vesicles in ischemic myocardium.

The sequence of contraction-relaxation for myocardial cells is believed to be linked to Ca2+ flux across the sarcoplasmic reticulum. Alterations of sarcoplasmic reticulum function during ischemia may result in depressing the myocardial contraction-relaxation sequence. This study examines the relationship between the membrane potential and Ca2+ flux across sarcoplasmic reticulum vesicles isolated from non-ischemic and ischemic myocardium. Ischemic myocardium was produced by ligating the coronary artery of swine hearts for 15 and 30 minutes. Membrane potential was determined by use of the fluorescence-sensitive dye, 3,3'-diethylthiadicarbocyanine, and Ca2+ uptake was studied spectrophotometrically with the use of murexide. Results are as follows: (1) membrane potential and Ca2+ uptake by sarcoplasmic reticulum from ischemic myocardium progressively decreased with the length of ischemia; and (2) preincubation of sarcoplasmic reticulum from non-ischemic myocardium with deoxycholate (0.01 approximately 0.09 percent) resulted in progressively decreasing membrane potential and Ca2+ uptake. Apparently a correlation exists between membrane potential and the rate of Ca2+ uptake. These results suggest that membrane characteristics of sarcoplasmic reticulum are altered within as early as 15 minutes of the onset of ischemia. Alteration of membrane permeability in sarcoplasmic reticulum from ischemic myocardium may be responsible for the observed decrease in membrane potential and Ca2+ uptake.

Animals↗
PubMedDate not supplied

Chronobiology of human blood pressure in the light of static (room-restricted) automatic monitoring.

Systematic 24-h automatic physiologic monitoring has obvious merits, even without rhythmometry. It can lead more readily to the recognition of odd-hour blood pressure elevation (e.g., of 'evening' or 'morning' hypertension). Such a condition can constitute an initial diagnosis or it may be found under treatment that may seem to be satisfactory if its effects are assessed only on the basis of a conventional check at a casual, possibly 'wrong' time. The mere inspection of a 24-h record, however, does not necessarily allow one to make objective quantitative global statements as to a change in pattern, e.g., after a given intervention. This paper illustrates how by rhythmometry, some of the uncertainties of a subjective interpretation of a record may be removed by practitioners of medicine, as well as basic scientists interested in mechanisms of blood pressure variability. This is possible since a large part of blood pressure variability can be accounted for by its circadian periodic behavior. We herein present a methodology for data collection and analysis that allows the objective quantification of blood pressure rhythm parameters in health and disease and the derivation of reference standards for such parameters. The chronobiologic approach thus makes it possible to define 'hypertension' objectively, and to distinguish between 'mesor-' and 'amplitude-hypertension', i.e., between an elevation in overall mean and one in the predictable extent of variability. Moreover, chronobiology has shown that mesor-hypertension may be preceded by an elevation in circadian amplitude only (amplitude-hypertension). Parameter tests readily allow the assessment, in relation to an objective reference standard, of these conditions, with a defined probability. Similarly, response to drug or non-drug therapy can be established and a given intervention optimized by timing treatment. Using chronobiologic tools in cardiovascular research provides new insights into possible mechanisms underlying mesor- and amplitude-hypertension. The teaching of the chronobiology of blood pressure and autorhythmometry in schools has been proven to be feasible and has been recommended as a step toward self-help for health care.

Adolescent↗
PubMedDate not supplied

Glucocorticoid effects on the embryonic chick heart. II. Alteration of oxidative metabolism.

The injection of cortisol phosphate (0.5 mg per egg) onto the chorioallantoic membrane of embryonic chicks at 12 days incubation depresses the rate of oxygen consumption in heart mitochondria isolated from the chicks 24 or 48 hours after the injection as compared to a saline injected control. The oxygen consumption is depressed using either reduced nicotinamide-adenine dinucleotide (NADH)-linked or flavin adenine dinucleotide (FADH)-linked substrates. The progressive inhibition of oxidation and adenosine triphosphate (ATP) production rate is related to the time after cortisol is injected. The treated mitochondria appear to function differently when NADH-linked and FADH-linked respiratory substrates are compared. Using NADH-linked substrates (site 1), adenosine diphosphate (ADP) was phosphorylated by mitochondria, even though the rate of phosphorylation was decreased; however, when FADH-linked substrates were used, incomplete phosphorylation was observed. The rate and the extent of calcium accumulation by embryonic chick heart mitochondria were also depressed by cortisol. These data suggest a defect in phosphorylation at site 2 following cortisol treatment but not at the site 1 linked energy transducing step. Whether these impairments of mitochondrial function result from catabolic turnover of the mitochondrial membrane components, excessive calcium accumulation by the mitochondria, or from the digestion of mitochondrial constituents, has not been delineated.

Adenosine Diphosphate↗