Search PubMed⌕ Search

Biomedical subjects

S Christakos

Publications and source records attributed to S Christakos.

113 records · Page 7Linked to original sources
PubMed1977

Re-entry ectopic ventricular rhythm caused by artificial pacing.

Two cases with coupled ectopic ventricular rhythm associated with artificial pacing are presented. The premature ventricular beats appeared at a fixed distance from the R of the previous electrical stimulus complex and when pacing was stopped ventricular arrest occurred. This provides strong evidence that the ectopic ventricular beats were dependent on the electrical stimulus and therefore that they were produced by its re-entry. It was observed that the re-entry phenomenon occurred at low rates. This arrhythmia even persisted after the permanent pacing and was successfully suppressed by procainamide in both cases.

Aged↗
PubMed1976

Neonatal modification of endocrine functions and mammary carcinogenesis in the rat.

Effects of neonatal androgenization or neonatal ovariectomy in female rats on endocrine functions and mammary tumourigenesis are examined. Pituitary gonadotrophin contents (both LH and FSH) are significantly lower in neonatally androgenized rats (TT) and significantly increased in neonatally ovariectomized rats (NO) when compared with controls of the same age. Plasma and pituitary prolactin levels are higher in TT rats than in the control rats of the same age, but the difference is not significant. Mammary tumours developing in TT rats after DMBA treatment are predominantly fibroadenomata, and lactogenesis in TT rats occurs almost entirely in those receiving DMBA treatment. Neonatal ovariectomy in female rats protects against subsequent induction of mammary cnacer by DMBA. The relationship between neonatal modification of endocrine functions and mammary tumourigenesis is discussed.

9,10-Dimethyl-1,2-benzanthracene↗
PubMedDate not supplied

Age and gender effects on 1,25-dihydroxyvitamin D3-regulated gene expression.

Several factors involved in regulation of bone mineral metabolism were compared in male and female Fischer 344 rats of different ages (1, 2.5, 6, and 18 months). Plasma 1,25-(OH)2D3 concentrations decreased with age in rats of both genders. Abundance of calbindin-D28K and its mRNA in kidney and calbindin-D9K and its mRNA in duodenum also decreased with age in both male and female rats. Renal 24-hydroxylase activity and 24-hydroxylase mRNA content were elevated significantly in 18-month-old males and females, compared with younger ages. These data suggest that increased renal catabolism of 1,25-(OH)2D3 may be responsible for low plasma 1,25-(OH)2D3 concentrations observed in older animals. Plasma PTH and 1,25-(OH)2D3 concentrations, renal 24-hydroxylase enzyme activity and 24-hydroxylase mRNA content, duodenal 24-hydroxylase mRNA abundance, and duodenal calbindin-D9K and calbindin-D9K mRNA content were greater in males than in females at 2.5 months of age. Lower plasma 1,25-(OH)2D3 concentrations in females seem to explain observed gender differences in expression of 1,25-(OH)2D3-stimulated genes. The combined effects of these gender differences at ages when peak bone density is being developed may contribute to the greater incidence of osteoporosis in females than in males.

Aging↗