1977
DOI: 10.1016/0006-8993(77)90008-7
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Effect of reserpine on cell proliferation in the developing rat brain: A biochemical study

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Cited by 51 publications
(6 citation statements)
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“…The transitory presence of fibers containing a large amount of DBH in this intense proliferation area could suggest a relationship between NA and cell division. However, this relationship al ready taken in account by others [13,17,18] has not been clearly demonstrated yet.…”
Section: Discussionmentioning
confidence: 90%
“…The transitory presence of fibers containing a large amount of DBH in this intense proliferation area could suggest a relationship between NA and cell division. However, this relationship al ready taken in account by others [13,17,18] has not been clearly demonstrated yet.…”
Section: Discussionmentioning
confidence: 90%
“…The cerebellar thymidine kinase activ ity is 30 times higher than that of the fore brain [25]. While in the forebrain the most important proliferative area, the ventricular subependymal layer produces exclusively glia cells, in the external granular layer of cere bellum only small neurons are formed and a lesser amount of glia is produced by the internal granular layer [20].…”
Section: Discussionmentioning
confidence: 94%
“…In contrast with our previous studies using drugs to deplete catecholamines such as reserpine, 6-OHDA and tetrabenazine [24][25][26], which are CNS depressants or used for chemi cal sympathectomy, in this study we used amphetamine, an antidepressant with pro foundly different chemical structure and be havioral effect. Since amphetamine has been reported to disturb development [15] and pro-tein synthesis in the brain at high doses [22,35], and is also known to deplete norepineph rine stores in brain [16], it seemed to be of interest to investigate whether any changes of [3H]-thymidine incorporation could be de tected in the developing rat brain after amphe tamine treatment.…”
Section: Introductionmentioning
confidence: 99%
“…Homogenates were centrifuged at 35,000 x g for 30 min at O°C and the resulting supernatants were removed and frozen. On the day of the assay, supernatants were thawed and duplicate aliquots analyzed for thymidine kinase activity by the radioisotopic method of Patel et al (1977) with minor modifications. Reagent blanks with homogenization buffer used in place of tissue extracts were analyzed in parallel in each assay and results corrected by subtracting blank values from all sample values in that assay.…”
Section: Methodsmentioning
confidence: 99%