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1.  We investigated potassium (K) transport in vitro across four major segments of the avian intestine. In normal fed birds, the most proximal segment, the duodenum, had very low unidirectional rates of K transport (Jms 6.7 nEq·cm–2·hr–1; Jsm 7.7 nEq·cm–2·hr–1). The jejunum had the greatest unidirectional K flux of the segments studied (Jms 36.6 and Jsm 85.5 nEq·cm–2·hr–1), and this segment showed a net K secretion (48.9 nEq·cm–2·hr–1). The ileum had a significantly lower Jms (16.5 nEq·cm–2·hr–1) than did the jejunum, and this segment also showed a net K secretion (28 nEq·cm–2·hr–1). Potassium transport across the mucosal surface of the colon was very low (Jms 7.7 nEq·cm–2·hr–1) while the Jsm flux was relatively large, giving a net K secretion of 45.7 nEq·cm–2·hr–1.
2.  When tissues were bathed in solutions having approximately normal in vivo K concentrations on both sides of the membranes and open circuit PD (to simulate in vivo conditions), the jejunum was the only segment that showed a net K absorption (83 nEq·cm–2·hr–1).
3.  When birds were fed a low K diet for 2 weeks, the colon showed the greatest response with Jms for K increasing 12 fold over control.
4.  From these studies we conclude that in normal birds the duodenum appears to be relatively impermeable to K and does not appear to play a significant role in K transport. However, the jejunum by virtue of its relatively greater permeability to K, the total length of jejunum comprising the intestine (66%), and the in vivo K gradients, seems to be most important in K absorption in the normal bird. The ileum and colon were major sites of K secretion in vitro and appear to be most important in intestinal regulation of K transport in response to changes in the dietary K load.
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  • 1.1. The intestinal nerve of the fowl was studied in vitro.
  • 2.2. A significantly larger amplitude spike discharge was recorded in side branches of the nerve which innervate the gut when the aboral end of the main nerve trunk was stimulated than when the oral end was stimulated.
  • 3.3. Postganglionic autonomic neurones innervating the smooth muscle of the ileum are not located in the intestinal nerve. Evidence is presented, however, supporting the idea that such neurones innervating the rectum are located in the rectal position of the nerve.
  • 4.4. The increase in intraluminal pressure and circular muscle tension in the ileum was greater following aboral nerve stimulation than following oral nerve stimulation.
  • 5.5. It is suggested that excitatory efferent nerve fibres ascend the intestinal nerve to innervate the ileum.
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1. Pieces of small intestine taken from chickens subjected previously to continuous selection, relaxed selection or no selection for rapid growth were used to estimate villus surface area and microvillus development to determine what effects genetic selection might have on factors controlling intestinal function. 2. Crypt size and the rates at which enterocytes migrated out of crypts were also measured, after injection of tritiated thymidine, to determine the time course of microvillus elongation. 3. Differences in growth rates measured between highly selected, relaxed selected or unselected birds were found to be correlated with parallel changes in villus surface area. Selection for growth did not change the density, dimensions or pattern of development of enterocyte microvilli. Microvilli did, however, produce a maximal 20-fold increase in villus surface area under all conditions. 4. Crypt size and enterocyte migration rates did not vary significantly between tissue taken from unselected and relaxed selected chickens. Tissue taken from highly selected birds had a crypt size and enterocyte migration rate 40% higher than values found for the other two groups of chickens. 5. The possibility that early genetic selection increased growth potential by uncoupling diet-induced changes on crypt hyperplasia from secondary effects on villus structure, and that later selection increased growth potential by increasing appetite, is discussed.  相似文献   

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Pizzari T  Froman DP  Birkhead TR 《Heredity》2002,88(2):112-116
Although much attention has been recently directed to sexual selection arising after insemination from sexual promiscuity, little is known about the mechanisms determining reproductive success after insemination, and the way these mechanisms interact with each other and with selective mechanisms occurring before insemination: mate choice and mate acquisition. Here, we briefly review the findings of an on-going study investigating the mechanisms generating variation in reproductive success at both a pre- and a post-insemination stage in the domestic fowl. Female preference consistently favours socially dominant males before and after insemination. However, although social status mediates the number of sperm that a male inseminates into a female, dominant males may inseminate sperm of lower fertilising quality than their subordinates. We argue that mitochondrial genes may contribute to determine sperm quality, and speculate that the maternal control of mitochondrial genes may prevent sexual selection from operating on males, thus explaining both the lack of a positive correlation between social dominance and sperm quality and the maintenance of variation in male quality in the fowl.  相似文献   

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Summary A lectin histochemical study was performed on formalin-fixed paraffin-embedded tissues of duodenum, jejunum, ileum, caecum and colon from six fasted and six non-fasted 8-week-old chickens (Gallus domesticus). The purpose of this study was to identifyin situ the pattern of carbohydrate residues present on the luminal surface of the intestinal epithelium. Ten biotinylated lectins with different sugar specificities were used as probes, and avidin—biotin—peroxidase complex (ABC) was used as a visualant. The most significant finding was the binding pattern ofLens culinaris agglutinin to various segments of the intestines. The luminal surface of the small intestinal epithelium did not stain with this lectin. In the colon the luminal surface was lightly stained, while the caecal luminal surface was intensely stained. Throughout the intestine the luminal surface stained withCanavalia ensiformis agglutinin,Ricinus communis agglutinin-I and wheatgerm agglutinin, but it did not stain withDolichos biflorus agglutinin. These findings indicated that, throughout the intestine, the luminal surface contains glycoconjugates with eitherN- orO-linked glycoprotein, or both, with terminal non-reducing -galactosyl and sialyl residues. Furthermore, the caecal surface is rich inN-linked glycoproteins with an -(16)-linked fucosyl residue near the glycosidic linkage. The potential significance of these observations and the role of glycoconjugates in host—parasite interaction (i.e.Eimeria sp. versusGallus domesticus) are discussed.  相似文献   

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  • 1.1. Immature birds were deprived of water either by removing the source or denying them access.
  • 2.2. Birds tended to become hypocorticosteronaemic when the water source was removed and hypercorticosteronaemic when access to the water was denied.
  • 3.3. It is concluded that psychological factors are important in determining the response to putative Stressors.
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Studies of ovulation in the perfused ovary of the fowl (Gallus domesticus)   总被引:1,自引:0,他引:1  
A system was developed for the in-vitro perfusion of the fowl ovary. The ovaries were isolated 16-18 h before expected ovulation of the first follicle of a clutch sequence and perfused at 41 degrees C with Eagle's culture medium containing L-thyroxine and insulin. The efferent perfusion pressure was maintained at 30-40 mmHg. This model was used to investigate the mechanism of ovulation. Addition of LH (1 U) to the perfusate induced ovulation (46%) but LH (1 U) + FSH (1 U) was more effective (88%; P less than 0.05). Progesterone at 100 micrograms alone also induced ovulation (80%). Clomiphene prevented gonadotrophin-induced ovulation. These results suggest that progesterone may act directly on the ovary as a final hormone to induce ovulation in the domestic fowl.  相似文献   

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The steroidogenic potential of various physiological compartments within the ovary of the hen were examined using in vitro systems. Three-hour incubations of individual whole small follicles (less than 1 mm-1 cm) or 100,000 collagenase-dispersed theca cells of the five largest ovarian follicles (F1-F5) were conducted in 1 ml of Medium 199 at 37 degrees C in the presence and absence of luteinizing hormone (LH) (0.39, 0.78, 1.56, 3.13 and 6.25 ng), progesterone (5 ng), and dehydroepiandrosterone (DHEA, 5 ng). Steroid output was measured by radioimmunoassay of incubation media. Progesterone was not produced by small follicles although they are a major source of DHEA and estradiol and a significant source of androstenedione. Output of DHEA, androstenedione and estradiol was highly stimulated by LH. The substrate for androstenedione and estradiol in small follicles is probably DHEA. Output of DHEA and androstenedione in theca cells of F2-F5 was stimulated by LH in a dose-related manner. A dose-response relationship between estradiol output and the concentration of LH in media was not apparent in theca cells from F2-F5. Steroidogenesis in theca tissue of large follicles occurs predominantly via the delta 4 pathway. The ability of these theca cells to metabolize progesterone to androstenedione is lost between 36 and 12 h before ovulation. Their ability to metabolize DHEA to androstenedione is still present 12 h before ovulation. Aromatase activity is significantly reduced between 36 and 12 h before ovulation. These data indicate that both large and small follicles can be stimulated by LH. The small follicles are the major source of estrogen. As the large yolky follicles mature, steroidogenesis shifts from the delta 5 to the delta 4 pathway. By 12 h before ovulation, the F1 follicle has lost the ability to convert progesterone to androstenedione. The inability of the largest ovarian follicle to convert progesterone to androstenedione contributes at least in part to the preovulatory increase in the plasma concentration of progesterone that generates the preovulatory LH surge by positive feedback.  相似文献   

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Evidence is presented to demonstrate the presence of W chromosome-specific repetitive DNA sequences in the female White Leghorn chicken, Gallus g. domesticus, based on two different experimental approaches. First, 3H-labelled, female chicken DNA was hybridized with excess, unlabelled, mercurated, male DNA, and unhybridized single-stranded 3H-DNA (3H-SHU-DNA) was recovered by SH-Sepharose and hydroxyapatite column chromatography. Approximately 24% of the hybridizable 3H-SHU-DNA was female-specific and localized on the W chromosome. The second approach was to examine female-specific DNA fragments among the digests of chicken DNA with various restriction endonucleases. Among them, we found that digestion with XhoI produced two prominent female-specific bands of 0.60 kb (= kilobase pairs) and 1.1 kb. The 0.60 kb fragment was isolated and 3H-labelled by nick-translation. Female-specificity of the 3H-XhoI—0.60 kb DNA was judged to be at least 95% under the conditions of hybridization with membrane filter-bound DNA. Presence of amplified XhoI—0.60 kb DNA on the W chromosome seems to be limited to different lines of G. g. domesticus and no such repeat was detected in three species belonging to other genera in the order Galliformes and in three species belonging to other avian orders.  相似文献   

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Summary Both avian corticosteroid hormones, aldosterone and corticosterone, increased short-circuit current across the wall of the ceca of the domestic fowl (Gallus domesticus) in vitro. About 80% of this short-circuit current was inhibited by the Na-channel blocking drug amiloride. Corticosterone was about ten times less potent than aldosterone in increasing short-circuit current and it exerted a similar maximal effect. Cortisol (an endogenous corticosteroid hormone in mammals but not birds) was about ten times less potent than corticosterone and this difference appeared to reflect the presence of the 17-OH group in cortisol. Carbenoxolene, which inhibits 11-hydroxysteroid dehydrogenase, increased the effect of corticosterone. This effect is consistent with inhibition of the metabolism of corticosterone to 11-dehydrocorticosterone. The latter was found to be about 100 times less potent than corticosterone. The effects of both aldosterone and corticosterone (also dexamethasone) were abolished by the mineralocorticoid receptor antagonist spironolactone. The results suggest that corticosterone has an effect similar to aldosterone but in vivo its action may be depressed by the activity of 11-hydroxysteroid dehydrogenase. The sensitivity of the cecal preparations to corticosterone indicates that this hormone could contribute to the regulation of transcecal Na transport (absorption) in vivo.Abbreviations 11-HSD 11-Hydroxysteroid dehydrogenase - sc short-circuit current - KRB Krebs bicarbonate solution  相似文献   

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