AI Article Synopsis

  • Intrauterine growth retardation was induced in rats by clamping the uterine artery during gestation, which allowed researchers to study its effect on DNA synthesis in the hippocampus and cerebellum.
  • The study measured DNA accumulation by tracking the incorporation of methyl-[14C]thymidine and analyzing thymidine metabolites, revealing defects in phosphorylation and reduced thymidine use in hypotrophic rats that could hinder DNA synthesis.
  • A catch-up growth phenomenon was observed in different timing across brain regions, with a strong correlation found between morphological studies and biochemical data regarding the development of neurons and glial cells.

Article Abstract

Intrauterine growth retardation was induced in the rat by clamping the uterine artery on day 17 of gestation. The effect of hypotrophy on DNA synthesis was studied in two different cerebral structures: hippocampus and cerebellum. Accumulation of DNA in these structures was biochemically measured in parallel to the incorporation of methyl-[14C]thymidine into nucleic acid at different ages and correlated with autoradiography. The various metabolites of thymidine in acid-soluble fraction were determined by using chromatographic procedures. Phosphorylation defects or reduced utilization of thymidine were found in hypotrophic rats and may delay the DNA synthesis. An essay of catch-up occurred with a different timing according to the cerebral region studied. A morphological and DNA synthesis. An essay of catch-up occurred with a different timing according to the cerebral region studied. A morphological and autoradiographic study after incorporation of [3H]thymidine was carried out in parallel. The neuronal and glial components of cytogenesis were analyzed separately and a good correlation was observed between histological and biochemical data in both groups of animals.

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http://dx.doi.org/10.1016/0165-3806(85)90217-2DOI Listing

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