Effect of contraceptive steroids on mammary gland of beagle dog and its relevance to human carcinogenicity.
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Biomedical subjects
Publications and source records attributed to M F el-Etreby.
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Using the immunoperoxidase technique and antisera to the specific beta (beta) subunits of bovine and rat TSH, selective immunocytochemical staining was localized in a specific cell population in the pars distalis of the dog pituitary gland. These TSH cells were found to be positive to aldehyde fuchsin, alcian blue, periodic acid-Schiff (PAS) and aniline blue. With the performic acid-alcian blue (pH 0.2) -PAS-orange G procedure these cells stained blue-purple, demonstrating FSH/LH cells (blue or turquoise), ACTH/MSH cells (red-purple) and PRL cells (orange-red). The TSH cells were further differentiated from other functional cell types of the pars distalis on the basis of their typical cytological features, intraglandular distribution and by immunocytochemical double staining. In the pars distalis of adult male dogs the TSH cells were mostly shown to be smaller in size and less numerous than in bitches in the anestrous phase of the sexual cycle. Moreover, cytological alterations in the immunoreactive thyrotrophs in the pituitary of male and female dogs generally paralleled the spontaneous changes in thyroid function associated with thyroid atrophy and/or pituitary insufficiency, and thyroid hyperplasia or goiter. In conclusion, because of their specificity and high potency, the antisera to the beta-subunits of bovine and rat TSH represent an effective tool for the selective immunocytochemical localization of TSH in the dog pituitary. This allows the study of the morphology and function of TSH cells under different physiological, pathological and experimental conditions.
Using the immunoperoxidase technique and specific homologous antisera to highly purified canine prolactin (PRL) and canine growth hormone (GH), selective immunocytochemical staining was localized in two different cell types in the pars distalis of the dog pituitary gland. The specificity and validity of both antisera were demonstrated by elimination of their immunostaining capacify after prior absorption with their respective antigens, while absorption with other antigens failed to decrease staining intensity. This was further confirmed by studying the immunologic behavior of both antisera in the agar gel double diffusion immunoprecipitin test and by competitive radioactive binding analysis. The specific heterologous antisera to ovine PRL and human GH were shown to be just as useful as antisera to canine hormones for immunocytochemical demonstration of the individuality of PRL and GH cells in the dog pituitary. This confirms the validity and specific of our hitherto heterologous immunocytochemical procedure. However, because of their high potency the anti-canine GH and anti-canine PRL sera seem to be more efficient for immunocytochemical staining of the dog pituitary. The immunoreactive PRL and GH cells were also distinguished with reasonable certainity in two different populations of acidophils according to their tinctorial affinity. Both cell types differed further from each other in respect of their relative proportion, morphology and topography, which were variously pronounced for each sex.
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