Dominance status and adrenocortical reactivity to stress in squirrel monkeys (Saimiri sciureus)

Squirrel monkeys (Saimiri sciureus, Iquitos) were exposed to a sequence of three stresses: A live snake, ether anesthesia, and physical restraint. Plasma cortisol concentrations were determined both following each stress exposure and before and after the sequence of stresses. Dominant males demonstrated lower unstressed plasma cortisol levels than subordinates. Although the form of the relationship between adrenal activity and social dominance differs for the types of stress, dominant animals always show the greatest adrenal reactivity to stress.     

The transmural distribution of coronary blood flow during maximal vasodilation.

Experiments were performed to examine the transmural distribution of the coronary blood flow during maximal vasodilation and when intramyocardial pressures were either minimized (cardiac arrest) or maximized (tachycardia). The results reveal a gradient of vascular resistance across the ventricular wall that favors flow to the subendocardium in the presence of maximal vasodilation. Thus a flow gradient favoring the subendocardium was seen when intramyocardial pressures were minimized by cardiac arrest, but when tissue pressures were maximized through tachycardia this gradient of flow was reversed.     

Blood group, serum protein and red cell enzyme groups of Amerindian populations in Colombia

Red cell samples from persons belonging to four Amerindian linguistic groups in Colombia were investigated for genetic variants in eight blood group systems: for three of the groups investigations were extended to ten red cell enzyme and four serum protein systems. The groups studied are the Noanama (including six Empera) of the Rio Siquirisua and Rio Docampado on the Pacific lowlands and the Cofan, Ingano and Siona Indians of the Upper Rio Putumayo and its tributaries to the east of the Andes. Only blood group O was present among two of the groups and the same groups were 100% Kp(b +), k in the Kell system. Di(a +) frequencies were high in three groups and there was marked variation between groups for the MNS, Rh, P, Lewis and Duffy systems. Polymorphism in all the three linguistic groups studied for serum proteins and red cell enzymes was present only in the red cell acid phosphatase, phosphoglucomutase (locus-1) and haptoglobin systems. 6-phosphogluconate dehydrogenase was polymorphic in the Noanama, and caeruloplasmin was polymorphic in the Ingano linguistic group. In addition two persons belonging to the Cofan linguistic group revealed the presence of an “atypical” component in the lactate dehydrogenase system. No variation was found in the other six red cell enzyme and two serum protein systems. Comparison with published data on red cell enzyme and serum protein groups for other South American Amerindian populations shows the Colombian populations studied here most closely resemble the Cayapo of Brazil.     

The distribution of red cell enzyme and serum protein groups in a population of Dani (Pit River,West Irian)

Summary Blood samples from a series of Dani speaking persons from Pit River, West Irian have been studied for genetic variants in 14 red cell enzyme and 5 serum protein systems. Four of the red cell enzyme systems were polymorphic: acid phosphatase, 6 phosphogluconate dehydrogenase, adenosine deaminase and phosphoglucomutase (locus 1). Two of the serum protein systems, haptoglobin and transferrin, were polymorphic. In the other systems three MDH New Guinea-1 variants were detected and two persons with variants, one MS and one SS, in the protease inhibitor system were detected also. An unusual variant in the PGM (locus 2) system has not yet been adequately identified. All other systems were monomorphic.

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Zusammenfassung Blutproben einer Anzahl Dani-sprechender Personen des Pit River-Gebietes in West-Irian wurden auf genetische Varianten in 14 Erythrocytenenzym- und 5 Serumprotein-Systemen untersucht. 4 der Erythrocytenenzym-Systeme waren polymorph: Saure Phosphatase, 6PGD, Adenosindeaminase und Phospho-glucomutase₁. Zwei der Serum-protein-Systeme, Haptoglobin und Transferrin, waren polymorph. In den anderen Systemen wurden 3 MDH New Guinea-1-Varianten gefunden, ebenso wie 2 Personen mit Varianten, 1 MS und 1 SS, im Pi-System. Eine ungewöhnliche Variante im PGM₂-System ist noch nicht ausreichend bestimmt worden. Alle anderen Systeme waren monomorph.

     

Induction, differentiation and oncogenesis

Eukaroytic cytodifferentiation usually leads to stable end-states. However, evidence on embryonic induction in amphibia supports the view that the initial stages of cellular maturation following induction of differentiation are comparatively labile, stability being a property acquired during maturation.Early developing cells may therefore retain the capacity for reversion to their previous, less developed, condition and a proportion of any group of induced cells may do so. Possible implications of such a phenomenon are explored, using two kinetic models of reversion. It is concluded that reversion is a possible mechanism in leukaemogenesis and other forms of oncogenesis.     

The Stoichiometry of Respiration-driven Potassium Transport in Corn Mitochondria

Determinations were made for corn (Zea mays L., WF9-Tms × M14) mitochondria of the stoichiometric relationship between K⁺ transport and bond energy produced in respiration (K⁺/~ ratio). With inward pumping of potassium acetate activated by NADH oxidation, the initial rate of K⁺ transported into the sucrose inaccessible space varied between 0.58 and 0.97 K⁺/~, assuming 2 high energy bond equivalents per NADH oxidized. Only small amounts of H⁺ were ejected. Valinomycin did not alter the ratio.     

Photosystem II regulation of macromolecule synthesis in the blue-green alga Aphanocapsa 6714.

Polymers synthesized by heterotrophically growing (glucose as carbon source) cultures of Aphanocapsa 6714 were compared with polymers synthesized in photosynthetically grown cultures. Loss of photosystem II by dark incubation, or inhibition of light-grown cells with the photosystem II-specific inhibitor dichlorophenylmethylurea, caused an 80 to 90% reduction in the rate of lipid and total ribonucleic acid synthesis, and more than a 90% reduction in the rate of protein synthesis. In contrast, glycogen synthesis was reduced only about 50% in dark cells and less than 30% in dichlorphenylmethylurea-inhibited cells. After longer heterotrophic growth, glycogen became the major component, whereas in photosynthetically grown cultures protein was the major constituent. 14C (from 14CO2 and/or [14C]glucose) assimilated into protein by heterotrophically grown cells was found in amino acids in nearly the same proportions as in photosynthetically grown cells. Thus, routes of biosynthesis available to autotropic cells were also available to heterotrophic cultures, but the supply of carbon precursors to those pathways was greatly reduced. The limited biosynthesis in heterotrophic cells was not due to a limitation for cellular energy. The adenylates were maintained at nearly the same concentrations (and hence the energy charge also) as in photosynthetic cells. The concentration of reduced nicotinamide adenine dinucleotide phosphate was higher in heterotrophic (dark) cells than in photosynthetic cells. From rates of CO2 fixation and/or glycogen biosynthesis it was determined that stationary-phase cells expended approximately 835, 165, and less than 42 nmol of adenosine 5'-triphosphate per mg (dry weight) of algae per 30 min during photosynthetic, photoheterotrophic, and chemoheterotrophic metabolism, respectively. Analysis of the soluble metabolite pools in dark heterotrophic cultures by double-labeling experiments revealed rapid equilibration of 14C through the monophosphate pools, but much slower movement of label into the diphosphate pools of fructose-1,6-diphosphate and sedoheptulose-1,7-diphosphate. Carbon did flow into 3-phosphoglycerate in the dark; however, the initial rate was low and the concentration of this metabolite soon fell to an undetectable level. In photosynthetic cells, 14C quickly equilibrated throughout all the intermediates of the reductive pentose cycle, in particular, into 3-phosphoglycerate. Analysis of glucose-6-phosphate dehydrogenase in cell extracts showed that the enzyme was very sensitive to product inhibition by reduced nicotinamide adenine dinucleotide.     

Pulmonary angiotensin-converting enzyme. Interspecies homology and inhibition by heterologous antibody in vivo.

Goat antibody against pure rabbit pulmonary angiotensin-converting enzyme was used to probe homology of converting enzymes from other species. Immunologically cross-reactive material was found in detergent-solubilized extracts of lung particles from rat, guinea pig, and dog by double immunodiffusion, radioimmunoassay, and inhibition of enzyme activity. No homology was demonstrable with bovine, frog, or chicken lung extracts. Antibodies from different individual goats yielded comparable estimates of homology by immunodiffusion and radioimmunoassay. In contrast, they varied greatly in extent and specificity of their inhibitory action on heterologous enzyme activity. The vasopressor effect of angiotensin I and the vasodepressor effect of bradykinin were diminished and potentiated, respectively, in rats treated with anti-rabbit enzyme antibody. A smaller but significant immune-dependent inhibition of the vasopressor response to angiotensin II was also observed.