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1.
The journal of experimental biology ; 206: 3707-3718, Oct. 2003. tab, graf
Artigo em Inglês | MedCarib | ID: med-17613

RESUMO

We examined the mechanistic basis for two whole-animal performance traits, aerobic capacity and burst speed, in six laboratory-reared Trinidadian guppy populations from different native drainages with contrasting levels of predation. Using within- and between-population variation, we tested whether variation in organs and organ systems (heart, gill and swimming motor mass) and the activities of several enzymes that support locomotion (citrate synthetase, lactate dehydrogenase and myofibrillar ATPase) are correlated with aerobic performance (maximum rates of oxygen consumption, (O(2)max)) or burst performance (maximum swim speed during escape responses). We also tested for associations between physiological traits and habitat type (different drainages and predation levels). Organ size and enzyme activities showed substantial size-independent variation, and both performance measures were strongly correlated to body size. After accounting for size effects, neither burst nor aerobic performance was strongly correlated to any organ size or enzymatic variable, or to each other. Two principal components (PCI, PC2) in both males and females accounted for most of the variance in the organ size and enzymatic variables. In both sexes, heart and gill mass tended to covary and were negatively associated with citrate synthetase and lactate dehydrogenase activity. In males (but not females), variation in aerobic performance was weakly but significantly correlated to variation in PC1, suggesting that heart and gill mass scale positively with (O(2)max). Neither of the component variables and no single morphological or enzymatic trait was correlated to burst speed in either sex. Evolutionary changes in important life history traits occur rapidly in guppy populations subjected to different predation intensities (high mortality in downstream sites inhabited by large predatory fish; low mortality in upstream sites lacking large predators). We found significant differences between stream drainages in all morphological variables and most enzymatic variables, but only the mass of the swimming motor and LDH activity were significantly affected by predation regime. Overall, our data show that microevolution has occurred in the physiological foundations of locomotor performance in guppies, but evolutionary changes in physiology do not closely correspond to the predation-induced changes in life history parameters.


Assuntos
Animais , Masculino , Feminino , Estudo Comparativo , Research Support, Non-U.S. Gov't , Research Support, U.S. Gov't, Non-P.H.S. , Trifosfato de Adenosina/metabolismo , Análise de Variância , Citrato (si)-Sintase/metabolismo , Meio Ambiente , Poecilia/anatomia & histologia , Poecilia/fisiologia , Reação de Fuga , Brânquias , L-Lactato Desidrogenase/metabolismo , Músculo Esquelético/anatomia & histologia , Tamanho do Órgão , Consumo de Oxigênio/fisiologia , Análise de Componente Principal , Fatores Sexuais , Natação/fisiologia , Trinidad e Tobago
4.
Biochem Pharmacol ; 11: 593-602, 1962. tab, gra
Artigo em Inglês | MedCarib | ID: med-3579

RESUMO

Slices of rat liver and suspensions of ascites cells were used to determine the effects of antihistamine drugs upon ion movements; it was shown that these drugs inhibit uptake of potassium in such systems. The relationship between phosphoproteins and these effects was also investigated, and there appeared to be a direct relationship between protein phosphorylation and water and ion movements; this relationship is not mediated by effects on ATP levels or turnover rates. The nature of the protein fraction that takes up 32P and shows diminished turnover in the presence of the drugs has been established by partial hydrolysis and identification of radioactive phosphoserine by chromatography on ion-exchange columns and upon paper(AU)


Assuntos
21003 , Ratos , Antagonistas dos Receptores Histamínicos H1/efeitos adversos , Íons , Fosfoproteínas , Ascite , Fígado/efeitos dos fármacos , Deficiência de Potássio , Trifosfato de Adenosina , Fosforilação
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