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We have identified numerous similar examples among bacteria, plants, and animals in which the benefits versus risks of DHA/EPA appear to dictate the ecological distribution pattern of organisms that produce these fatty acids. , 2004). As discussed later, the levels and distribution patterns of DHA in tissues of a short-lived mouse are dramatically different than the distribution pattern in a long-lived human, with most human cells containing only traces of Membranes of Deep-Sea Bacteria as Surrogates for Mitochondria 27 DHA compared to the high levels of DHA found in cells of mice.
J. Neurochem. 57:348–51. Chen, H. , T. K. Tseng, and L. W. Ding. 2009. Intravenous paraquat poisoning. J. Chin. Med. Assoc. 72:547–50. , and S. Przedborski. 2003. Parkinson’s disease: mechanisms and models. Neuron 39:889–909. Harman, D. 1956. Aging: a theory based on free radical and radiation chemistry. J. Gerontol. 11:298–300. Harman, D. 1972. The biologic clock: the mitochondria? J. Am. Geriatr. Soc. 20:145–47. Langston, J. , P. Ballard, J. W. Tetrud, et al. 1983. Chronic parkinsonism in humans due to a product of meperidine-analog synthesis.
A requirement in mitochondria for a consistent and abundant supply of energy provided by the host cell. • In B. stearothermophilus, high temperature increases rates of respiration, energy production, and proton leakage, whereas human mitochondria operating at a constant 37°C have evolved to respond quickly to signals reflecting changes in energy demand by modulating rates of respiration. Mitochondria, especially in ectothermic animals, are also capable of membrane adaptation in response to changes in the environment and energy demand.
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