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Sex differences in the LH responses to chicken LHRH-I and -II in the domestic fowl.

Maximal incremental changes in plasma LH were compared in adult hens and cockerels after i.v. injection of chicken (c) LHRH-I (pGlu1-His2-Trp3-Ser4-Tyr5-Gly6-Leu7-Gln8-Pro9-Gly10-N H2) or cLHRH-II (pGlu1-His2-Trp3-Ser4-His5-Gly6-Trp7-Tyr8-Pro9-G ly10-NH2). The LH response to cLHRH-I and -II was more rapid and greater in cockerels than in hens. The potencies of the two decapeptides were the same in cockerels but different in hens. Relative to cLHRH-I, the potency of cLHRH-II was 0.91 (0.6-1.2; 95% confidence limits) in cockerels and 36.5 (16.8-128.6) in hens. The greater potency of cLHRH-II relative to cLHRH-I in the hen than in the cockerel could not be accounted for by sex differences in the half-lives of the decapeptides in the peripheral circulation. The half-lives of both decapeptides in hens and cockerels ranged between 2.42 and 3.77 min. It is concluded that the interaction between LHRH-I and -II and the gonadotrophs is sexually differentiated in the domestic fowl. A new homologous radioimmunoassay was established for cLH. As in other chicken LH radioimmunoassays, there was evidence of cross-reactivity with TSH.

Animals↗

Fine structure of the pancreatic islets in domestic fowl with special reference to the cell type and secretion.

The pancreatic islets of domestic fowl were investigated by electron microscope. The following results were obtained. 1. The A islet is composed of a great many A cells and a few D cells. It also contained only a few B cells which are situated mainly along capillaries. 2. On the contrary, the B islet is composed of a great many B cells and a few D cells. It also contained only a few A cells in its periphary. 3. Immature secretory granules within the Golgi complex are almost the same in size, shape and density among the three types of islet cells. Since there are quite distinct differences in these properties of mature secretory granules in the cytoplasm among the three types of islet cells, there may be a difference in the mode of maturation process among the three. 4. These granules are released from the three types of islet cells through a mechanism termed as emiocytosis.

Animals↗

Fauna, flora, fowl, and fruit: effects of the Columbian Exchange on the allergic response of New and Old World inhabitants.

The Columbian Exchange has been described as "the most important event in human history since the end of the Ice Age." This interchange of many species of fauna, flora, fowl, and fruits resulted in new encounters between New and Old World inhabitants. Prominent among these were manifestations of allergic reactions to many of the new substances. Little imagination is required to reflect on what these substances, added to or detracted from both the New and Old World lifestyles, habits, and diets. The numerous peas, vegetable seeds, and grasses, such as sugarcane, introduced during Columbus' later voyages, made an enormous difference in the lives of New World inhabitants, as did the introduction of the cow and horse, not to mention substances such as coconuts and bananas, that are now intimately associated with the Caribbean and the Bahamas. This article focuses on some the more important exchange substances and emphasizes many forms of anaphylaxis: asthma, food allergy, hypersensitivity pneumonitis, chronic bronchitis, rhinitis, serum sickness, and other conditions that developed in both New and Old World inhabitants. To mention only a few examples, the Europeans introduced to the New World potential dangers such as honeybees (anaphylaxis). It also gave the New World the cow and the horse (serum sickness), which became the constant companion of Columbus' Indians and the American cowboy. It gave the Italians their thick red gravy, and the New World its pizza (food allergy). The Caribbean received bananas and coconuts and the New World embraced coffee (caffeine addiction). On the other hand, the exchange also caused Europeans to begin puffing away on tobacco.

Animals↗

Proventricular glands in fowl.

Some researchers have already described the fowl proventriculus. However, we believed there was a need for detailed carbohydrate histochemical investigations on the same glands. Moreover, some researchers had erred about the lamina muscularis mucosae. The results of these investigations are as follows. 1. The proventricular glands consist of both superficial and profound gastric glands. 2. The superficial glands are distributed in the lamina propria mucosae while the profound glands exist in the tela submucosa. 3. The superficial glands are simple, branched tubular glands. The columnar glandular cells are arranged in a simple layer and react strongly to PAS, AB (pH 2.5 and 0.5). These appear to be dark purple when they are stained with PAS-AB (pH 2.5). Some other methods have also been tried. 4. Judging from the data 3), the superficial gastric glands contain neutral, weak and strong acids, sulfuric and acid mucopolysaccharides, sialomucin, and II and III neutral mucus type. 5. Glandular cells in the body and basal portions of the superficial gastric glands contain a large number of fine pepsinogen granules. 6. Judging from the data of 3)-5), we believe that the superficial gastric glands are undifferentiated gastric glands and that they are same kinds of glands that are found in mammals. 7. A large number of profound gastric glands fill the tela submucosa. They are compound tubular glands, and are composed of many glandular alveoli. Their columnar glandular cells are arranged in a simple layer. 8. These glandular cells react moderately to PAS, negatively to AB (pH 2.5 and 0.5) and PAS-AB (pH 2.5). Moreover, we observed some other reactions.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Circadian rhythmicity in the 'basal' pancreatic secretion of the domestic fowl.

The interdigestive pancreatic exocrine secretion of the domestic fowl has been studied following the cosine-vector analysis. For the flow of pancreatic juice the crest phase was at 1040 and the sample amplitude was 2.26 microliter/min. For the amylase output the crest phase was at 1128 and the sample amplitude was 0.297 U.A.A./min. Both parameters are characterized by a phase-and frequency-synchronized rhythm whose period must be close to 24 hr.

Amylases↗

DNA sequence of the fowl adenovirus serotype 10 short fiber gene.

The complete nucleotide sequence and map location of the short fiber gene of fowl adenovirus serotype 10 (FAV-10) strain CFA20 was determined. The coding sequence of the short fiber gene was found to be 1383 bp, encoding a putative polypeptide of 461 amino acids. The gene was located between 69.2 to 71.7 map units on the FAV-10 genome. A consensus splice acceptor site was located 30 bp upstream of the putative translation start codon and a polyA recognition sequence was located 24 bp downstream of the translation stop codon, signaling the end of late transcription unit five.

Adenoviridae↗

DNA sequence analysis of the genes for the fowl adenovirus serotype 10 putative 33K and pVIII.

The nucleotide sequence and genomic location of the fowl adenovirus serotype 10 (FAV-10) putative 33K and precursor protein VIII (pVIII) genes have been determined. The total genomic region sequenced was 1814 base pairs (bp) in length with the 33K coding region occupying the sequence from nucleotides 44 to 634 and the pVIII coding region nucleotides 949 to 1689. The location of both the 33K and pVIII genes have the same positional organization as their human adenovirus (HAV) counterparts which is 3 prime (3') to the 100K gene. Along with the 100K the 33K and pVIII form the late transcription unit 4 (L4). The FAV-10 putative 33K coding region could encode a polypeptide of 196 amino acids in length with a relative molecular mass of 21.9 kilodaltons (kDa) while the pVIII produces a polypeptide of 246 amino acids with a calculated relative mass of 26.7 kDa. Two possible splice acceptor sites were identified one 5' to the 33K and one 5' to the pVIII coding regions. A putative poly A recognition sequence of AATAAA was identified 3' to the pVIII, signaling the end of the L4 transcription unit.

Amino Acid Sequence↗

Liver- and muscle amino-acid concentrations during the development of domestic fowl.

The concentrations of free amino acids in liver, leg muscle and wing muscle of developing domestic fowl chicks were measured and compared with those of adults. Leg and breast muscles showed a remarkably parallel pattern of change in free-amino-acid concentrations during development up to day 5 after hatching, in agreement with their lack of differentiation up to day 5. Liver free-amino-acid concentration pattern with the development were very similar to those of the muscles, in significant difference with Mammals. Adult free tissue amino acids were lower than those of developing chicks. Most changes in amino-acid concentration in chick tissues were observed around hatching, and have been tentatively attributed to changes in diet. Combined amino acids changed very little during the period studied in muscles and liver. Taurine constituted a very big share of total amino acids.

Age Factors↗

Genetic-dependent alterations in adrenal stress response and adrenocortical cell function of the domestic fowl (Gallus domesticus).

Strain-dependent differences in adrenocortical function were investigated in male White Leghorn domestic fowl. Adrenocortical function of Cornell K strain (K) (genetic control), autosomal dwarf strain (ADW), and sex-linked recessive dwarf strain (SLD) was evaluated in vivo by measuring plasma corticosterone and in vitro by measuring acute (2 hr) corticosterone production by enriched adrenocortical cell populations. Regardless of strain, there was an age-dependent decrease (27-57%) in plasma corticosterone from 1 to 12 weeks of age. However, there was a tendency for plasma corticosterone values of ADW and SLD to be, respectively, greater and less than that of K. In addition, at 12 weeks of age, plasma corticosterone responses of ADW and SLD to transient heat stress (50 degrees C, 30 min) were, respectively, 22.8% greater and 15.9% less than that of K. Strain differences in adrenal weight and relative adrenal weight (mg% body wt) were also apparent. At 12 weeks of age, adrenal weights of ADW and SLD were, respectively, 33 and 42% less than that of K, whereas relative adrenal weights were, respectively, 27.6% greater and 22.4% less than that of K. In addition there were strain-dependent differences in adrenocortical function at the cellular level. Although there were no consistent strain differences in basal and maximal corticosterone production by cells, there were strain differences in cellular sensitivity to ACTH and pregnenolone. On an equal cell concentration basis, the half-maximal steroidogenic concentrations (ED50 values or effective doses for 50% maximal effect) of ACTH for ADW and SLD adrenocortical cells were, respectively, 0.23 and 2.07 times the ED50 value for K cells. In addition, the ED50 value of pregnenolone for ADW cells was 0.46 times that for K and SLD cells. Since ED50 values are a measure of cellular sensitivity (the greater the ED50 value the lesser the cellular sensitivity), the order of sensitivity to ACTH was ADW greater than K greater than SLD and the order of sensitivity to pregnenolone was ADW greater than K = SLD. However, there were no strain differences in ED50 values of 8-bromo-cyclic AMP. These data suggest that strain differences in plasma corticosterone response to stress are, in part, due to differences in relative adrenal weight and differences in adrenocortical cell function.

Adrenal Cortex↗

Ontogenic corticosteroidogenesis of the domestic fowl: response of isolated adrenocortical cells.

Ontogenic adrenocortical function of the domestic was investigated using adrenocortical cells isolated from embryonic chicks (18, 19, 20, and 21 days old) and male and female posthatch birds (1 day, 1 week, and 3 weeks old). Production of the predominant corticosteroids secreted by the chicken adrenal gland, corticosterone, cortisol, and aldosterone, was measured by radioimmunoassay after 2-hr incubation of cells with or without steroidogenic agents. Approaching hatch, basal and maximal ACTH-(1-24) (ACTH)-induced corticosteroid production increased steadily and peaked around 1 day posthatch (5-18 times and 3-9 times, respectively, the production values at 18 days embryonic life). Thereafter, corticosteroid production values decreased steadily to 3 weeks posthatch. Corticosterone predominated over the ages studied: Maximal ACTH-induced corticosterone production averaged 52 and 115 times the production values of aldosterone and cortisol, respectively. In addition, maximal ACTH-induced aldosterone production was roughly 2.2 times greater than cortisol production over the ages studied except for a short-lived, disproportionately greater aldosterone production at 1 day posthatch. In addition to perihatch and age-related differences in cellular corticosteroid production, there were also differences in cellular sensitivity to steroidogenic agents as indicated by the differences in half-maximal steroidogenic concentration values (ED50 values) of the steroidogenic agents. Sensitivity to ACTH increased 2.7 times from Day 18 of embryonic life to 1 day posthatch and then decreased steadily to 3 weeks posthatch. In addition, sensitivity to 8-bromo-cAMP (8-Br-cAMP) increased abruptly at 1 day posthatch (nearly 3 times) but then remained constant thereafter. However, a consistent change in cellular sensitivity to 25-hydroxycholesterol was not observed until 3 weeks posthatch (an increase in sensitivity of 3 times that at Day 18 of embryonic life). These data of cellular sensitivity suggest that there were distinct development and maturational alterations in the cellular loci at which ACTH, 8-Br-cAMP, and 25-hydroxycholesterol acted. Thus, during the transition from embryonic to postembryonic life of the domestic fowl, there are alterations in adrenocortical cell steroidogenic capacity and in the function of some cellular loci comprising the corticosteroidogenic pathway.

8-Bromo Cyclic Adenosine Monophosphate↗

Adrenocortical function of the domestic fowl: effects of orchiectomy and androgen replacement.

The effect of orchiectomy and androgen replacement on cockerel adrenocortical function was investigated. Orchiectomized cockerels (2 weeks old) were implanted with Silastic tubing containing various amounts of one of the following steroids: cholesterol, testosterone (T), androstenedione (A4), and 5 alpha-dihydrotestosterone (DHT). Birds were administered additional implants, containing doses of steroids equivalent to those of the initial implants, at 4 and 8 weeks of treatment (i.e., 6 and 10 weeks of age). Sham-operated cockerels administered empty implants served as intact controls for comparison of data. Animals were killed after 10 weeks of treatment (12 weeks old). Trunk plasma corticosterone (B) and plasma T, and B production by collagenase-isolated adrenocortical cells incubated briefly (2 hr) with or without steroidogenic agents were measured by radioimmunoassay. Orchiectomy with implantation of the inert sterol, cholesterol (hereafter referred to as orchiectomy), did not alter plasma B concentrations and did not affect basal cellular B production or cellular B production induced by a maximal steroidogenic concentration of ACTH or that maximally supported by 25-hydroxycholesterol. However, orchiectomy did lower maximal 8-bromo-cyclic AMP-induced B production by 30%. Low-implant doses of A4 (1-cm implant) and T (0.3-cm implant), that maintained comb growth, lowered plasma B concentrations by 24-42%, whereas a high-implant dose of T (3-cm implant) and all implant doses of DHT had no effect on plasma B concentrations. Thus, androgen replacement had different effects on plasma B depending on the type of androgen and the implant dose. In contrast, androgen replacement consistently suppressed basal and maximal ACTH-induced cellular B production regardless of the type of androgen. Furthermore, the degree of suppression was dose-dependent. These results suggest that the differential effect of androgen replacement on plasma B concentrations was due to differences in the clearance of circulating B and/or differences in blood volume. In addition, the present study suggests that in the absence of the testes, androgens are suppressants of adrenocortical cell function in the domestic fowl.

8-Bromo Cyclic Adenosine Monophosphate↗

The effects of environmental temperature on fertility of the domestic fowl.

Three experiments were conducted to determine the influence of environmental temperature upon the fertility of domestic fowl. It was found that a cold environmental temperature depressed testes growth and delayed spermatogenesis in maturing cockerels. There was also a highly significant difference in the fertility of mature males kept at different environmental temperatures. Males kept at 19 degrees C. had higher fertility than males kept in either 30 degrees or 8 degrees C. The effects of environmental temperature on female fertility was also studied. Fertility was significantly lower in the hens kept at 30 degrees C. than that of similar groups held at an environment of 8 degrees C.

Animals↗

Incomplete dominance of the gene for naked neck in domestic fowl.

The autosomal gene for naked neck in domestic fowl has been shown to be incompletely dominant. Heterozygotes characteristically have an isolated tuft of feathers on the ventral side of the neck above the crop. Homozygotes lack this tuft completely, or it may be reduced to a very few pinfeathers or small feathers.

Animals↗

The influence of short term exposure to two different environmental temperatures on electrolyte concentrations of fowl semen.

The concentration of some of the electrolytes found in fowl semen changed when birds were transferred from a temperature environment of 19 degrees C to either 8 degrees or 30 degrees C. The pH of the semen obtained from males transferred to the 30 degrees C. environment significantly decreased as opposed to a significant increase in the pH of the semen obtained from males transferred to the 8 degrees C. environment. Sodium and potassium concentrations significantly increased in whole semen in both transfer groups, while magnesium increased significantly only in whole semen from males transferred to the 8 degrees C. environment. Sodium increased in seminal plasma when the males transferred from 19 degrees C. environment to the 8 degrees C. environment. The data indicate that an abrupt change to either a warmer or colder environment causes a change in electrolyte concentration of cock semen.

Animals↗

The efficacy of chlordimeform for the control of the northern fowl mite, Ornithonyssus sylvarium (Canestrini and Fanzago) (Acarina, Dermanyssidae).

Chlordimeform applied as a 0.06% low pressure spray controlled the northern fowl mite (NFM) for at least 90 days. Tetrachlorvinphos applied as a 0.5% low pressure spray was equally effective. Chi square analysis of NFM population estimates indicated that NFM populations on the untreated control birds stayed essentially the same throughout the test, whereas, the NFM populations on both acaricide-treated groups were significantly lowered by the seventh day of the test (P less than .01). Chlordimeform seemed to work more slowly than tetrachlorvinphos in controlling NFM.

Amidines↗

Connective tissue constituents of the fowl. Effects of exogenous estrogen.

The levels of connective tissue constituents (hexosamine, hexuronic acid, hexose and hydroxyproline) and the composition of isolated mucopolysaccharide-peptide complexes were determined in some organs and tissue of male and female fowl treated and not treated with estradiol-17beta. Most of the changes occurred in the male. Estrogen administration brought statistically significant increases in the contents of hexosamine and hexuronic acid in the cartilage of the male and of hexose in the spleen of both males and females. It also increased the hydroxyproline in the testis and in the cartilage of the male. Estrogen decreased the content of hexosamine in the combs of both males and females, and in the wattle of the female, of hexuronic acid, hexose and hydroxyproline in the liver of the male, and hydroxyproline in the breast muscle of the male. Hexosamine, sialic acid, lipid and protein contents of blood sera of estrogenized birds were substantially higher than that of the controls. Gas liquid chromatography of the lipids of the tissues indicated that estrogen administration brought about an increase in the proportion of the unsaturated fraction to the total fatty acid content.

Animals↗

Evaluation of Rofenaid and a commercial bacterin for prevention of cranial form of fowl cholera in turkeys.

Rofenaid, a potentiated sulfadimethoxine at drug concentrations of 0.04, 0.02, and 0.01% in feed, a combination of vaccination with a commercial bacterin and 0.01% potentiated sulfadimethoxine (Rofenaid), and vaccination separately, significantly (P less than 0.05) increased livability of turkeys experimentally induced with the cranial form of fowl cholera as compared to that of the nonmedicated nonvaccinated exposed turkeys. Turkeys were exposed by the administration of Pasteurella multocida (isolate 8579) in the drinking water.

Administration, Oral↗

The effect of caproic acid, handling technique and storage times on the fertility of fowl spermatozoa.

The effects of three levels of caproic acid in glycine-citrate extender on preservation of fertilizing capacity of fowl spermatozoa were tested. Extended semen stored for 6 and 28 hours was used for insemination in diluted or reconcentrated forms. The results indicated that semen stored in the extender with the highest concentration of caproic acid provided superior fertility and showed the importance of proper handling of hens during insemination.

Animals↗