1992
DOI: 10.1038/jcbfm.1992.141
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Maturation of Cerebral Oxidative Metabolism in the Cat: A Cytochrome Oxidase Histochemistry Study

Abstract: The maturation of brain oxidative capacity was studied in kittens, using cytochrome oxidase histochemistry, at different ages throughout development. Optical densitometry values of reacted tissue were obtained for 50 different structures of the brain. In general, most structures reached adult levels of oxidative capacity by 30 days of age with some motor areas (e.g., cerebellum, red nucleus) exhibiting adult values as early as 7 days of age. Thereafter, some structures (e.g., basal ganglia, thalamus) exhibited… Show more

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Cited by 36 publications
(16 citation statements)
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“…the oxidative metabolic capacity matures prior to LCMRgiu [23] and in the rabbit reaches adult lev els during the 3rd week of life [38]. In the present study hydrocephalus was induced prior to full maturation [38][39][40], but our first CO data were taken at 32 days.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…the oxidative metabolic capacity matures prior to LCMRgiu [23] and in the rabbit reaches adult lev els during the 3rd week of life [38]. In the present study hydrocephalus was induced prior to full maturation [38][39][40], but our first CO data were taken at 32 days.…”
Section: Discussionmentioning
confidence: 99%
“…From previous studies in humans [20. 21] and animals [22][23][24][25], it is known that the glucose demand and oxidative metabolic capacity of the develop ing brain differs with age. Therefore, it is likely that the brain will respond differently to both hydrocephalus and shunting according to its stage of development.…”
Section: Introductionmentioning
confidence: 99%
“…In the present study, oxidative capacity was quantified by performing cytochrome oxidase histochemistry with techniques similar to those described by Hovda et al (1992). Briefly, as for the cerebral blood flow experiments, the animals were killed and the brains were quickly removed, frozen and stored at -75°C.…”
Section: Histochemical Measure Of Oxidative Metabolismmentioning
confidence: 99%
“…For cytochrome oxidase (CO) histochemistry, slides were incubated for 90 min in 50 ml of 0.1 M phosphate buffer (pH 7.4) containing 30 mg of 3,3'-diaminobenzidine and 5 mg of cytochrome caccording to the method of Hovda et al (1992). For succinate dehydrogenase (SDH) histochemistry, slides were incubated for 45 min in 50 ml of 0.06 M phosphate buffer (pH 7.0) containing 20 mg of nitro blue tetrazolium and 0.68 gm of succinate (Kieman, 1990).…”
Section: Polysynaptic Regulation Of Glutamate Receptors and Mitochondmentioning
confidence: 99%