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Evidence that forskolin activates turkey erythrocyte adenylate cyclase through a noncatalytic site.

The diterpene forskolin has been reported to activate adenylate cyclase in a manner consistent with an interaction at the catalytic unit. However, some of its actions are more consistent with an interaction at the coupling unit that links the hormone receptor to the adenylate cyclase activity. This report adds support to the latter possibility. Under conditions that lead to stimulation of adenylate cyclase in turkey erythrocyte membranes by GTP, forskolin also becomes more active. Additional evidence to support an influence of forskolin upon adenylate cyclase via the GTP-coupling protein N includes the following: (i) forskolin, at submaximal concentrations, leads to enhanced sensitivity and responsiveness of isoproterenol-dependent adenylate cyclase activity in turkey erythrocyte membranes; (ii) under specified conditions, the nucleotide GDP, an inhibitor of the stimulating nucleotide GTP and its analog, guanyl imidodiphosphate (Gpp(NH)p), also markedly inhibits the action of forskolin; (iii) both Gpp(NH)p and forskolin are associated with a decrease in agonist affinity for the beta-adrenergic receptor. However, actions of forskolin in the turkey erythrocyte are not identical to those of GTP: (i) forskolin is never as potent as Gpp(NH)p in activating adenylate cyclase; (ii) the magnitude of synergism between isoproterenol and forskolin is not equal to that observed with isoproterenol and Gpp(NH)p; (iii) at high concentrations, forskolin inhibits antagonist binding to the beta-receptor. Forskolin appears to have several sites of action in the turkey erythrocyte membrane, including an influence upon the adenylate cyclase regulatory protein N.

Adenylyl Cyclases↗

Effects of estrogen and progesterone on serum prolactin and luteinizing hormone levels in ovariectomized turkeys (Meleagris gallopavo).

Serum prolactin (PRL) and luteinizing hormone (LH) levels from mature female turkeys were determined following ovariectomy and daily subcutaneous injections for 4 or 9 days of 0.002-2.0 mg/kg estradiol benzoate (EB), 0.05-2.0 mg/kg progesterone (P), or their combinations. Serum PRL levels were increased (P less than 0.05) at the onset of sexual maturity in intact controls, but not in ovariectomized turkeys. Injection of 0.02 mg/kg EB into ovariectomized turkeys resulted in elevated (P less than 0.05) serum PRL levels after 8 treatment days. Higher doses failed to elicit a response of greater magnitude. EB at doses of 0.02-2.0 mg/kg reduced LH levels while 0.002 mg/kg EB increased LH levels above (P less than 0.05) those of ovariectomized controls. The 1.0-mg/kg P dose increased (P less than 0.05) serum PRL within 24-48 hr of administration while the 0.05-, 0.5-, or 2.0-mg/kg P doses failed to elicit a response. When P was injected in doses of 0.5-2.0 mg/kg, LH levels were decreased in a dose-response manner. The injection of EB combined with P had a variable effect on serum PRL levels. The 0.5- or 1.0-mg/kg dose of P facilitated (advanced in time) the rise in serum PRL level induced by 0.02 mg/kg of EB. In contrast, the positive feedback effect of 0.2 mg/kg of EB was blocked when administered with 0.5 mg/kg of P. Serum LH levels were dramatically decreased by all steroid combinations used. These results indicate that daily injections of EB and/or P in ovariectomized turkeys have a variable effect on serum PRL and LH levels depending upon the dose, the duration of treatment, or the ratio between EB and P.

Animals↗

Pulsatile secretion pattern of growth hormone in turkeys: effects of age and sex.

Male and female turkeys were cannulated through the jugular vein, and blood samples were withdrawn remotely at 10-min intervals for a period of 8 hr at two points in the post-hatch growth phase (4 and 14 weeks of age). Growth hormone (GH) concentration was determined for each sample by radioimmunoassay using a recombinant chicken growth hormone preparation as standard. Data were evaluated for age- and sex-related differences. Four-week-old male and female turkeys displayed a pulsatile pattern of GH secretion. Growth hormone secretory profile characteristics differed significantly between ages with regard to overall mean, number of peaks, amplitude of peaks, interval between peaks, baseline, and total GH detected. Male four-week-old turkeys had a peak amplitude significantly greater than that of females of the same age. Older (14-week-old) male turkeys demonstrated a significantly greater number of GH secretory peaks than females during the 8-hr sampling period; however, overall it did not appear that the older birds had an organized pattern of GH secretion above baseline levels.

Aging↗

The influence of the stomach on crop function and feeding behavior in domestic turkeys.

We tested the hypotheses that motility of the crop and muscular stomach are coordinated and that the stomach exerts primary control over crop filling and emptying in domestic turkeys. Simultaneous recordings of motility of the crop, esophagus, and stomach with implanted strain gauge transducers and visual observations of food passage using image intensification radiography revealed an inverse relationship between the frequency of stomach and crop contractions. Artificially filling the stomach of a fasted turkey with a food slurry prior to feeding did not increase crop filling during the first morning meal, but it did inhibit crop emptying in fasted turkeys by markedly reducing the number of crop contractions. Artificially filling the crop of fasted turkeys prior to the first morning meal did not decrease the amount of feeding activity or the total amount of food consumed during that meal. It is suggested that meal termination is associated with the degree of inhibition of esophageal peristalsis.

Animals↗

Histopathology of antitrochanteric degeneration in adult female turkeys of four strains of different mature size.

The left and right antitrochanters of 80 female turkeys of four strains were examined for histopathological changes at sexual maturity. Ten birds of each strain were fed ad libitum and 10 restricted to achieve 0.6 of the bodyweight of the ad libitum fed birds at 24 weeks old when the birds were photostimulated. Bodyweights at sexual maturity (28 to 31 weeks) for the four strains were 5.4, 6.5, 7.6 and 13.2 kg for restricted and 7.5, 9.0, 11.1 and 17.1 kg for ad libitum fed birds. The prevalence and severity of cartilage change increased with mature size and was lower in restricted turkeys then in turkeys fed ad libitum. The results showed that abnormal cartilage changes forming the basis of clinical disease occur in females. The prevalence and severity of lesions were directly related to bodyweight and were not limited to particular genotypes. Lesions were more severe in the centre of the antitrochanter, possibly because of forces exerted by the trochanter. Concentrations of basophilic cells in the hyaline cartilage were associated with the increased prevalence and severity of lesions in large turkeys and may be of significance in the development of osteochondrotic lesions in the antitrochanter.

Animals↗

Assessment of pain associated with degenerative hip disorders in adult male turkeys.

The extent to which degenerative hip disorders in adult male turkeys result in pain was investigated in a two-period crossover experiment. The birds in six pens received daily injections of an anti-inflammatory steroid (betamethasone) during week 1 and control injections of physiological saline in week 3. The turkeys in the other six pens received saline in week 1 and steroid in week 3. Behavioural observations of the birds during weeks 1 and 3 revealed that the steroid treatment resulted in more spontaneous activity. The steroid-treated birds also showed speedier movement in a sexual activity test in weeks 1 and 3. Post mortem examination revealed that all the turkeys were suffering from degenerative hip disorders. It is concluded that degenerative hip disorders in adult male turkeys result in a state of chronic pain which inhibits spontaneous activity and sexual activity.

Animals↗

Comparative studies on the structure of biliary immunoglobulins of some avian species. II. Antigenic properties of the biliary immunoglobulins of chicken, turkey, duck and goose.

Studies on the immunological cross-reactivity of the Igs+ from the bile of chicken and turkey (order Galliformes) as well as duck and goose (order Anseriformes) to Igs with antigenic known properties carried out by a series of RIA. Various class-specific anti-Ig sera produced in rabbits, guinea-pigs and mice were used. The following results were obtained: (1) A high extent of antigenic relationship between the chicken and turkey biliary Igs was demonstrated by a radiobinding system consisting of 125I-turkey biliary Ig and class-specific rabbit anti-turkey biliary Ig antibodies. The biliary Igs of duck and goose did not inhibit this antigen binding system. (2) The duck and goose biliary Igs were able to inhibit the binding of 125I-carp IgM to Fc-fragment-specific rabbit anti-carp IgM antibodies and of 125I-human IgM to Fc-fragment-specific guinea-pig anti-human IgM antibodies, respectively. (3) None of the biliary Igs show cross-reactive properties common with human and porcine IgA. That was detected by inhibition of the radio-binding system from 125I-human IgA and alpha chain-specific mouse anti-human IgA antibodies. Therefore, the conclusion was made that in anseriform birds IgM-like Igs are the secretory Igs, while in galiform birds biliary Igs with special antigenic properties occur.

Animals↗

Comparative studies on the structure of biliary immunoglobulins of some avian species. I. Physico-chemical properties of biliary immunoglobulins of chicken, turkey, duck and goose.

In pooled bile of chicken, turkey, duck and goose immunoglobulins (Igs)+ were found in relatively high amounts between 4.5 and 15.0 mg/ml (corresponding to 28 to 36% of the total protein contents). All biliary Ig fractions studied possess (H2L2)n structure estimated by SDS-PAGE. In chicken and turkey L chains are assumed to be non-covalently linked to the polymeric H chains. In duck and goose L chains are completely linked to H chains. The Mr of H chains are rather similar: 64 kDa for the Igs of chicken and turkey bile and 67 kDa for the biliary Igs of duck and goose. There are slight differences in the electrophoretic mobility: Chicken and turkey Igs are beta 1/alpha 2-globulins and the corresponding Ig fractions from duck and goose are beta 2-globulins.

Animals↗

Amino acid sequences and structures of chicken and turkey beta 2-microglobulin.

The complete amino acid sequences of chicken and turkey beta 2-microglobulins have been determined by analyses of tryptic, V8-proteolytic and cyanogen bromide fragments, and by N-terminal sequencing. Mass spectrometric analysis of chicken beta 2-microglobulin supports the sequence-derived Mr of 11,048. The higher apparent Mr obtained for the avian beta 2-microglobulins as compared to human beta 2-microglobulin by SDS-PAGE is not understood. Chicken and turkey beta 2-microglobulin consist of 98 residues and deviate at seven positions: 60, 66, 74-76, 78 and 82. The chicken and turkey sequences are identical to human beta 2-microglobulin at 46 and 47 positions, respectively, and to bovine beta 2-microglobulin at 47 positions, i.e. there is about 47% identity between avian and mammalian beta 2-microglobulins. The known X-ray crystallographic structures of bovine beta 2-microglobulin and human HLA-A2 complex suggest that the seven chicken to turkey differences are exposed to solvent in the avian MHC class I complex. The key residues of beta 2-microglobulin involved in alpha chain contacts within the MHC class I molecule are highly conserved between chicken and man. This explains that heterologous human beta 2-microglobulin can substitute the chicken beta 2-microglobulin in exchange studies with B-F (chicken MHC class I molecule), and suggests that the MHC class I structure is conserved over long evolutionary distances.

Amino Acid Sequence↗

Centrally and peripherally administered bombesin decreases food intake in turkeys.

The effects of intracerebroventricular (ICV) and intravenous injections of bombesin (BBS) on food intake were investigated in turkeys. Adult turkey hens were injected ICV with 50 to 1000 ng of BBS. In addition, the effect of pretreatment with the BBS antagonist [d-Arg1, D-Phe5, D-Trp7,9, Leu11]-substance P was investigated. To determine if BBS also had a peripheral site of action, 0.5 to 8 micrograms/kg body weight of BBS was injected IV into turkey poults. The ICV and IV injections of BBS decreased food and water intake in a dose-dependent manner. The most efficacious doses when injected ICV for decreasing food and water intake were 1000 and 500 ng, respectively, whereas 8 micrograms/kg was most efficacious in decreasing food intake when administered IV. The satiating effect of ICV-injected BBS could be attenuated with pretreatment with the BBS antagonist. The results of these studies suggest that BBS acts to decrease food and water intake in both the periphery and the central nervous systems of turkeys.

Animals↗

Protection of turkeys against haemorrhagic enteritis by monoclonal antibody and hexon immunization.

Virus-neutralizing monoclonal antibodies specific for the hexon of haemorrhagic enteritis virus (HEV), a turkey adenovirus, were examined for their ability to confer passive protection against haemorrhagic enteritis (HE) in turkeys. A high dose of antibody prevented clinical disease and reduced virus replication in experimentally infected birds. This suggests that virus neutralization might be an important mechanism for protection against HE. Subsequently, the use of the hexon protein as a subunit vaccine was investigated by immunizing birds with affinity-purified HEV hexon. The birds were tested for the appearance of hexon-specific antibodies in their sera, for protection from clinical disease, and prevention of virus replication after challenge with virulent HEV (HEV-V). Regardless of whether birds were immunized with native or denatured hexon, high ELISA antibody titres were produced to each immunogen. A virus-neutralizing antibody response was induced by immunization with the native hexon but not by immunization with the denatured protein. All turkeys twice immunized with a dose of at least 1 microgram, and four out of five birds immunized with two doses of 0.3 micrograms of purified native hexon, were protected against virus-induced disease and virus replication. In contrast, birds inoculated with denatured hexon were not protected. These results demonstrate the importance of the native (trimeric) structure of the hexon protein for eliciting a protective immune response. The impact of these results on the development of a vaccine for HE in turkeys produced by recombinant DNA technology is discussed.

Adenoviridae Infections↗

A type-specific avian influenza virus subunit vaccine for turkeys: induction of protective immunity to challenge infection.

The fraction NP/HA (nucleoprotein/haemagglutinin) obtained from n-octyl-beta-D-glucopyranoside-treated influenza A H5N2 virus was highly enriched for NP with residual haemagglutinin. This preparation was incorporated in ISCOMs. This potent 'immunostimulating complex' induced the production of high antibody titres in turkeys. The NP/HA ISCOMs preparation was found to protect turkeys from both homologous and heterologous challenge infection as shown by reduced viral titres in the lung and trachea of vaccinated turkeys. Clearance of the virus from trachea and lungs was seen at late stages of infection. The vaccine also induced a cellular immune response as measured by T-cell proliferation and a delayed-type hypersensitivity response. The results reported in this study demonstrate that the NP/HA ISCOM vaccine is capable of inducing type-specific immunity and that it has potential utility as a vaccine in turkeys.

Animals↗

Chlamydia psittaci in turkeys: pathogenesis of infections in avian serovars A, B and D.

At 7 days of age, 4 groups, each of twenty specific pathogen free turkeys kept in isolation units were inoculated by aerosol with the Texas Turkey strain (avian Chlamydia psittaci serovar D), strain 92/1293 (avian Chlamydia psittaci serovar D), strain 84/55 (avian Chlamydia psittaci serovar A) or strain 89/1326 (avian Chlamydia psittaci serovar B). A fifth group of 4 specific pathogen free turkeys were sham inoculated controls. At daily intervals for 10 days and then twice weekly up to 34 days post infection, one bird in each group was killed and the target tissues and cells for replication and the sequence of events of serovar A, B and D infections was examined. In these turkeys, the primary site of replication was the respiratory tract. Chlamydial replication could be detected in the respiratory tract on day 1 post inoculation (p.i.) for group A, on day 3 p.i. for group B and on day 1 to 2 p.i. for groups D1 and D2. Subsequently, there was chlamydaemia and localisation in the digestive tract, in one or more parenchymatous organs, in the pericardium and in the conjunctivae. Specific immunoperoxidase staining revealed chamydiae in these organs in epithelial cells and in monomorphonuclear cells in all infected groups. The monomorphonuclear cells were identified as macrophages by double immunofluorescence staining. Chlamydiae were present in the same tissues for serovars A and D, but could not be demonstrated in proventriculus, duodenum, pancreas, ovaries and testes for serovar B. Furthermore, the intensity of replication was similar for all serovars. However, for serovar B in comparison with the other serovars, the bacteria appeared in most tissues 1 to 6 days later and the maximal replication in these tissues occurred 3 to 4 days later.

Aerosols↗

Steroidogenic properties of isolated turkey adrenocortical cells.

Some functional properties of highly enriched turkey poult adrenocortical cells were characterized. Cells were incubated with various mammalian and avian ACTH analogues, 8-Br-cAMP, and 25-hydroxycholesterol for 2 hr. Corticosterone production and, where appropriate, cyclic AMP (cAMP) production were measured by radioimmunoassay. Human ACTH-(1-24) was the most efficacious and potent ACTH analogue for stimulating corticosterone and cAMP production, whereas turkey ACTH-(1-39) was among the least efficacious and least potent analogues. Maximal corticosterone production induced by 8-Br-cAMP and supported by 25-hydroxycholesterol was 67-109% greater than that induced by ACTH analogues. The data suggest that intracellular concentrations of cAMP-dependent factors and steroidogenic enzymes exceed those which are accessible to ACTH-activated cellular processes. In addition, there were sex-dependent contrasts in some functional parameters, despite the immature status of the birds. Basal corticosterone production of female cells was 19% greater than that of male cells, albeit maximal ACTH analogue-induced corticosterone production was not different between male and female cells. In contrast, maximal 8-Br-cAMP-induced and 25-hydroxycholesterol-supported corticosterone production of male cells were, respectively, 72 and 45% greater than that of female cells, thus suggesting greater intracellular concentrations of protein kinase A-dependent factors and steroidogenic enzymes in male cells compared to female cells. However, maximal ACTH-induced cAMP production of female cells was 21% greater than those of male cells, thus suggesting a compensatory mechanism in female cells. In addition, there were sex-dependent differences in sensitivity to ACTH as indicated by corticosterone and cAMP responses to ACTH analogues: sensitivity to ACTH as indicated by corticosterone and cAMP responses to ACTH analogues: sensitivity of male cells was 1.2-3.2 times that of female cells. A sex-dependent difference in ACTH-cell interaction, possibly including ACTH receptors, is implicated since there were no sex differences in cellular sensitivities to 8-Br-cAMP and 25-hydroxycholesterol. These data indicate that the turkey adrenal gland is amenable for the preparation of isolated adrenocortical cells that have functional integrity. Thus, turkey adrenocortical cells expand the in vitro repertoire for elucidating the regulatory mechanisms of avian adrenocortical function.

8-Bromo Cyclic Adenosine Monophosphate↗

Interaction of insulin-like growth factor I with turkey satellite cells and satellite cell-derived myotubes.

Satellite cells, isolated from the superficial pectoralis muscle of growing Nicholas tom turkeys, were cloned to obtain a pure population of myogenic cells. These cells proliferated rapidly and differentiated (fused) into myotubes typically containing 92-98% fused nuclei. Competitive binding assays were performed on near-confluent satellite cell or myotube cultures in 35 mm diameter wells by adding [125I]IGF-I along with increasing concentrations of unlabeled IGF-I, IGF-II, or insulin. Following incubation, the cultures were washed to remove the unbound hormones, solubilized with 0.5 N NaOH, and the radioactivity specifically bound was determined. Total and fused nuclei number as well as total protein were determined in parallel cultures. Our results indicate that turkey satellite cell and myotube cultures possess specific binding sites for IGF-I. Displacement of [125I]IGF-I was in the order of IGF-I greater than IGF-II greater than or equal to insulin. Although the [125I]IGF-I association constants were similar for turkey satellite cells and myotubes, a 2.8-fold decrease in the number of receptors per nuclei was observed as satellite cells differentiated into myotubes. The 50% inhibition constants for IGF-I, IGF-II, and insulin were 3.7 X 10(-9) M, 7.5 X 10(-8) M, and 8.7 X 10(-8) M for satellite cells and 3.1 X 10(-9) M, 7.5 X 10(-8) M, and 9.6 X 10(-8) M for myotubes, respectively. Receptor cross-linking analysis using disuccinimidyl suberate was performed on near-confluent satellite cell cultures incubated with [125I]IGF-I in the presence or absence of 1 X 10(-7) M IGF-I, IGF-II, or insulin. Receptor subunit species of Mr 130 kDa and 98 kDa were observed under reducing conditions (100 mM dithiothreitol) and at a Mr greater than 300 kDa (native receptor tetramer) under non-reduced conditions. Autoradiographic bands were displaced with IGF-I but not with equimolar levels of IGF-II or insulin. The results suggest that turkey satellite cells possess a type I IGF receptor.

Animals↗

Improvement of stored turkey semen quality as a result of He-Ne laser irradiation.

Two experiments were carried out to evaluate the effects of He-Ne laser irradiation at various energy doses on the quality of stored turkey semen. Four semen pools were used in Experiment 1. Each pool was divided into 10 aliquots, nine of which were irradiated with energy doses ranging from 0.144 to 10.8 J/cm2 while the tenth one was not irradiated (control). Each sample was evaluated for motility immediately after irradiation, 24 and 48 h later. Energy doses ranging from 3.24 to 5.4 J/cm2 had higher (P <0.01) sperm motility index (SMI) value compared to the control and samples irradiated with lower and higher laser doses. The energy dose of 3.96 J/cm2 was selected for Experiment 2 to obtain further insight on its effects on turkey sperm preservation for up to 60 h. Each pool of four semen was divided into two aliquots: one represented the control and the other one was irradiated with He-Ne laser at an energy dose of 3.96 J/cm2. Each sample was evaluated for motility and viability immediately after irradiation and then at 12 h intervals up to 60 h. The cell energy charge was also measured by HPLC. Exposure to 3.96 J/cm2 increased the SMI and viability of turkey semen stored for 60 h compared to the control (P <0.05). The cell energy charge of irradiated samples was 200% higher than in the control. Laser irradiation increased the longevity of stored turkey spermatozoa, and might be a useful technique to enhance semen quality in long-term storage.

Animals↗

The early steps of chloroform anaesthesia in Turkey during the Ottoman Empire in the 19th century.

OBJECTIVE: The aim of this study was to research the pioneering steps for the employment of chloroform in Turkey in comparison with the developments in the West i.e. in the United States and in Europe. The development of anaesthesiology in the West started in the first half of the 19th century. As an anaesthetic substance, ether was first employed in a medical operation by R. Liston in December 1846. But taking into consideration of its bronchially irritant effect, British gynaecologist Dr. J.Y. Simpson preferred to utilize chloroform in obstetrical operations in 1847. The paper aims at shedding light on the earlier steps for modern anaesthesiology in Turkey in that sense. METHODS: The survey used evaluation of archival documents, first hand-original sources such as the annual medical reports of the Medical School, books, official journals, and newspapers of the time, and also secondary sources concerned with the subject. RESULTS: In view of the findings of the survey, chloroform, as an anaesthetic material, began to be administered surgically in Turkey much earlier than it was already known. It was experienced and used in operations at the surgical clinic of the Imperial School of Medicine at the Capital city, Istanbul in 1848. The Crimean War (1853-1855) induced to the prevalent surgical use of chloroform in Istanbul on the soldiers back from the front. In other words, it was evidenced that surgeons started to make use of this anaesthetic substance in the Ottoman Empire, shortly after it was put into medical practice in Europe. CONCLUSION: This study deals with that phenomenal progress of chloroform anaesthesia in the medical history in Turkey during the second half of the 19th century.

Anesthesiology↗

Consanguineous marriages in the province of Antalya, Turkey.

To assess the trends in the frequency and the medical effects of consanguinity in the south coast of Turkish population using local and national data in the last 11 years. This cross-sectional study was carried out in Manavgat province, which is a major tourism center on the Mediterranean coast of Turkey. The authors studied consanguineous marriages in rural and urban population in the Mediterranean coast, Manavgat province, Turkey, via a 1500 random survey sample of married couples. There has been a significant increase in the incidence of consanguineous marriages in rural areas (40.7%) since 1989 in the southern population of Turkey. The results showed that the most frequent type of marriage was between the first cousins. It is found that there is no statistically significant difference between the consanguineous and non-consanguineous marriages in the different age groups. The results were discussed on the basis of educational status, reasons for having consanguineous marriages and the general medical effects as well as with the relation of congenital malformations. The custom of consanguineous unions in the Mediterranean population of Turkey is still extremely high, and preventive measures should be done to decrease its frequency and associated complications.

Consanguinity↗