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Changes in physiological reproductive states of female Long-Evans hooded rats were directly correlated with changes in the concentration of acidophilic and basophilic connective tissue granulated cells in the lamina propria of the duodenum. Acidophilic granulated cell numbers were significantly higher at estrus and metestrus than at other stages of the estrous cycle or in the immature state. apcidophilic granulated cell numbers during pregnancy were not significantly different from cell numbers quantified during metestrus, diestrus, or proestrus, but were significantly lower than cell numbers during estrus. Late lactation (21-25 days) was associated with significant decreases in the numbers of acidophilic granulated cells from numbers observed during the estrous cycle and during pregnancy. Basophilic granulated cell numbers did not differ significantly during the estrous cycle, although the highest numbers were observed during proestrus. Basophilic granulated cell numbers were significantly higher during pregnancy than during the estrous cycle. Basophilic granulated cell counts in late lactation were comparable to numbers quantified in estrus, metestrus, and diestrus, but were significantly lower than during proestrus and pregnancy.
Anat Rec 1975 Nov
PMID:Changes in numbers of acidophilic and basophilic connective tissue granulated cells in the intestine of the rat during the estrous cycle. 5 8

This report contains details of the code of practice for the control of contagious equine metritis (CEM) during the 1979 breeding season. It was prepared under the guidance of a scientific committee established by the Horserace Betting Levy Board under the chairmanship of Sir David Evans, FRS. The code is similar to the one introduced for the 1978 breeding season but takes into account the experience gained during the past 12 months. Following discussions with colleagues in Ireland it has been agreed that a similar code of practice will be introduced in the United Kingdom and Ireland so as to facilitate a uniform policy for the control of CEM. A summary of this report will be circulated to thoroughbred mare and stallion owners.
Vet Rec 1978 Oct 28
PMID:Contagious equine metritis: the present situation reviewed and a revised code of practice for its control. 72 4

The effects of UVL-B and/or testosterone replacemnt therapy are compared in normal and castrated rats in order to determine whether testosterone is required for UVL-B (290-315 nm) stimulation of melanogenesis in the testosterone-dependent epidermal melanocyte system of the scrotal skin of black Long Evans rats. Testosterone is not a prerequisite for UVL-B stimulation of melanocytes as in both castrates and normal animals the melanocytes respond to UVL-B by increases in size, length and number of dendrites (dendriticness), and tyrosinase activity (intensity of Dopa reaction). Addition of testosterone to castrates does enhance the effects of UVL-B. However, UVL-B with or without testosterone cannot maintain normal melanogenesis in rats irradiated immediately after castration nor can it restore normal melanogenesis following long term castration. Bth the amount of UVL nergy/exposure and the number of exposures are important variables in stimulation of the epidermal melanocytes. Administration of a dose of UVL-B to castrates in a single exposure is ineffective, while the same overall dose spread over several exposures increases the size and dendriticness of melanocytes. Testosterone and UVL-B act synergistically in affecting melanogenesis although neither singly nor in combination are they able to fully restore normal melanogenesis.
Anat Rec 1979 Jan
PMID:Testosterone and UVL-B stimulation of epidermal melanocytes in rat scrotal skin. 76 May 95

The anterior pituitary glands of male, adult Long Evans rats carried 5 days in the Space Shuttle Discovery (STS-29) have been compared with two groups of ground-based controls. All of the animals were part of a study (SE82-08) into the effects of gravity versus a microgravity environment on fracture healing. All had sustained a right, mid-shaft fibular osteotomy. The duration of the study was 10 days, and animals in all groups were weight bearing for the 5 days prior to shuttle lift off. The three experimental groups consisted of four rats each: flight (F) and two ground-based control groups, weight bearing (WB) and suspended (S). The suspension group was in a Holton/Sweeney head-down suspension apparatus (antiorthostatic) for the final 5 days of the study. The anterior pituitary glands of F and WB rats were essentially identical. The vasculature and parenchymal cells appeared unaffected in both instances. However, the anterior pituitary glands of S rats were dramatically altered. The vasculature was widely expanded with proteinaceous deposition covering the lumenal endothelial surfaces, and entrapping numerous platelets and aggregates of red blood cells. Parenchymal cells were highly vacuolated, occasionally with membranous vacuoles, but most often revealing large, clear cytoplasmic zones unlined by any membranes. Whereas profiles of exocytosis were numerous in F rats, and present in WB rats, they were essentially absent in S rats. These results indicate that weightlessness over a 5-day flight period does not influence the structural integrity of the anterior pituitary gland and may in fact promote secretory granule release. However, the head-down tilt model, frequently used to study fracture repair under conditions that mimic weightlessness, has a profound impact on the vasculature of the anterior pituitary gland which then affects the structural and functional characteristics of the parenchymal cells.
Anat Rec 1991 Nov
PMID:Pars distalis vasculature: Discovery Shuttle STS-29 rats compared to ground-based antiorthostatic rats. 176 16

Adult Long-Evans male rats were treated with various dosages of pure or technical grade 1,2-dibromo-3-chloropropane (DBCP), epichlorohydrin (Epi), or allyl chloride (AC) for 1, 3, or 6 months on a daily basis. AC, which is the substrate for the production of DBCP, and Epi, which is a contaminant and/or metabolite of DBCP, had no effect on any of the parameters of the male reproductive system studied. The deleterious effects on male reproduction are therefore attributable specifically to DBCP. The effects of DBCP were dose and duration dependent. At the lowest dose (1 mg/kg) DBCP did not have any discernible effects on the male reproductive system. By 3 months of treatment at the intermediate dose of 5 mg/kg, the morphology of the testis ranged from normally appearing seminiferous tubules to ones which contained Sertoli cells only. At 6 months of treatment there was a reduction in the weights of the testes and sexual accessory glands. At the highest dose, the majority of the rats showed advanced testicular regression by 1 month of treatment. The most extreme testicular regression was observed in the 6-month treatment group. Almost all of the seminiferous tubules of all of the rats were composed of Sertoli cells only. In some of the animals, a few isolated seminiferous tubules contained an occasional spermatogonium or primary spermatocyte. Some of the Leydig cells of the rats in this group showed morphological evidence of atrophy as evidenced by the clumping of chromatin and paucity of stainable cytoplasm. This was confirmed by lower levels of intratesticular testosterone, a significant reduction in the number of luteinizing hormone (LH) receptors and increased serum levels of LH and follicle-stimulating hormone (FSH). From these results we conclude that DBCP is a specific male gonadotoxin and that the effects are not a result of contamination or metabolism. The effects appear to be a direct action at the testicular level because feedback inhibition to the pituitary gland was adversely affected.
Anat Rec 1988 Dec
PMID:Morphological and biochemical changes in the adult male rat reproductive system following long-term treatment with 1,2-dibromo-3-chloropropane. 322 5

Mice were primed subcutaneously in the hind footpads with horseradish peroxidase (HRP) and boosted intravenously 10 weeks later. The appearance of cells with cytoplasmic anti-HRP antibody was studied in several lymph nodes. It appeared that following intravenous boosting antibody-forming cells appeared in significant numbers in the popliteal, the lumbar, and (in some animals) the sciatic lymph nodes exclusively. In the other lymph nodes examined specific antibody-forming cells were observed only occasionally. By subcutaneous injection of Evans blue in the hind footpads it was shown that the subcutis of the hind footpads of these animals is drained by the popliteal lymph nodes, the lumbar lymph nodes, and (to a lesser degree) the sciatic lymph nodes. The presence of trapped immune complexes within lymph node germinal centers was confined to these three nodes. Based on these findings, it is concluded that specific antibody-forming cells during the secondary response in these mice are induced exclusively in the lymph nodes draining the site of primary immunization.
Anat Rec 1984 Aug
PMID:Lymph node involvement in a humoral immune response. 654 Oct 6

Administration of trypan blue to pregnant Sprague-Dawley or Long-Evans rats, during an identical stage of embryogenesis, has been associated with malformations in 97 and 17% of the offspring, respectively (Gunberg, Anat. Rec. 1958, 130, 310). In the present study the comparative pharmacokinetics of trypan blue in the two strains were investigated. Female Sprague-Dawley and Long-Evans rats were injected sc with 10 mg trypan blue/rat [0.5 ml 2% (w/v) trypan blue in distilled water]. Blood samples were collected from the post-orbital plexus at times ranging from 5 min to 480 hr after dosing. The peak serum concentration of trypan blue was greater in Sprague-Dawley rats. Pharmacokinetic analyses of concentrations of trypan blue in serum resulted in fitting a two-compartment open model, with first order absorption, for both strains. Elimination of trypan blue from the central compartment was faster in Sprague-Dawley rats. This phenomenon was associated with a net movement out of the central compartment, predicted by the ratio of intercompartment rate constants. It is possible that the reported differences between the two strains in the teratogenic effects of trypan blue could be attributable, in part, to these observed pharmacokinetic dissimilarities.
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PMID:Comparative pharmacokinetics of trypan blue in female Sprague-Dawley and Long-Evans rats. 654 53

The effect of acid, basic, and organic extracts from Long Evans rat amniotic fluid (RAF) and from Swiss ICR mouse amniotic fluid (MAF) was studied on 15-day fetal mouse duodenal mucosa in organ culture. Amniotic fluids (20 ml) were lyophilized and extracted 1) with CHCl3:MeOH and the organic phase was evaporated; then 2), the residue was acidified with a solution of 0.1 N HCl in 10% acetic acid and the liquid phase was lyophilized; finally 3), 0.01 M NH4OH was added to the residue and the liquid phase was lyophilized. The product of each extraction was added to 20 ml of Trowell T8 medium. Acid and basic extracts of RAF and MAF have no effect on the formation of duodenal villi and crypts after 48 hours of culture. With the organic extract of MAF, small villi are present after 48 hours of culture and absorptive cells are poorly differentiated. With the organic extract of RAF, well-developed villi have differentiated after 48 hours of culture; moreover, crypts are present at the same stage and Paneth cells are identified within these crypts. During the 8-10 hour period, the explants cultured with the Trowell T8 medium supplemented with RAF or MAF organic extracts show a 35% increase in 3H-thymidine incorporation over the controls cultured with Trowell T8 medium alone. These results indicate that organic extracts from MAF and RAF are able to promote villus formation in undifferentiated explants from 15-day fetal mouse duodenum in organ culture. Furthermore, RAF organic extract contains a factor that can induce the formation of duodenal crypts and the differentiation of Paneth cells in culture at least 2 days before their normal appearance.
Anat Rec 1983 Jan
PMID:Extracts of rat amniotic fluid contain a potent inducer of intestinal crypt formation. 683 34

The ovaries of many mammals lie within membranous sacs called bursae ovaricae. In this study, we have examined the morphology of the bursa surrounding the hamster ovary using light and electron microscopy. The bursa is composed of three layers: (1) an inner, discontinuous bursal epithelium that faces the ovary; (2) a middle layer of connective tissue that contains fibroblasts, bundles of smooth muscle cells, and blood vessels; and (3) an outer, continuous epithelium that faces the peritoneal cavity. One side of the bursa has a thin layer of connective tissue, and because the ovary may be seen through it, we refer to this region of the bursa as the "window.' Elsewhere a thick layer of fat joins the connective tissue and blocks visualization of the ovary. Tracers (Evans blue and lanthanum) applied to the peritoneal surface do not penetrate beyond the peritoneal epithelium. Tracers injected into the bursal cavity penetrate all layers of the bursa, but do not pass through the peritoneal epithelium. Therefore, the bursa prevents tracer exchange between the bursal and peritoneal cavities, but exchange does take place between the bursal cavity and blood vessels within the bursa. We suggest that bundles of smooth muscle cells within the bursa may serve to regulate fluid volume and pressure within the bursal cavity. Possible functions of the complete bursa in the hamster are discussed.
Anat Rec 1981 Nov
PMID:Structure of bursae ovaricae surrounding the ovaries of golden hamster. 730 30

Retinoids, including all-trans-retinoic acid (RA) and its stereoisomer 9-cis-RA play important roles in regulating gene expression, through interactions with nuclear receptors, during embryonic development and in the maintenance of adult epithelial tissues (Chambon, P. (1995) Rec. Prog. Horm. Res. 50, 317-32; Mangelsdorf, D. J., and Evans, R. M. (1995) Cell 83, 841-850; Petkovich, M. (1992) Annu. Rev. Nutr. 12, 443-471). Evidence suggests that 4-hydroxylation of RA inside the target cell limits its biological activity and initiates a degradative process of RA leading to its eventual elimination. However, 18-hydroxylation and glucuronidation may also be important steps in this process. In this paper, we describe the cloning and characterization of the first mammalian retinoic acid-inducible retinoic acid-metabolizing cytochrome P450 (hP450RAI), which belongs to a novel class of cytochromes (CYP26). We demonstrate that hP450RAI is responsible for generation of several hydroxylated forms of RA, including 4-OH-RA, 4-oxo-RA, and 18-OH-RA. We also show that hP450RAI mRNA expression is highly induced by RA in certain human tumor cell lines and further show that RA-inducible RA metabolism may correlate with P450RAI expression. We conclude that this enzyme plays a key role in RA metabolism, functioning in a feedback loop where RA levels are controlled in an autoregulatory manner.
 ...
PMID:cDNA cloning of human retinoic acid-metabolizing enzyme (hP450RAI) identifies a novel family of cytochromes P450. 922 17


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