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Biomedical subjects

S Jackson

Publications and source records attributed to S Jackson.

At least 307 records · Page 17Linked to original sources
PubMed1985

Absorption, metabolism, and excretion studies of carbon 14- and tritium-labeled derivatives of a ketomethylene containing tripeptide.

Tritium and Carbon 14 analogs of the angiotensin converting enzyme inhibitor ketoACE were synthesized and their oral absorption, metabolism and excretion in rats were investigated. KetoACE, a ketomethylene analog of the tripeptide Bz-Phe-Gly-Pro, was slowly absorbed at a 35% level upon oral administration. It is rapidly eliminated from the blood with a half-life of about 10 minutes. Its excretion is primarily via the bile duct and it is excreted as 80% unchanged drug. The only identified metabolite consisting of 5-10% of the excreted radioactivity was determined to be the reduced ketoACE in which the ketone group was reduced to a hydroxyl.

Angiotensin-Converting Enzyme Inhibitors↗
PubMed1985

Pro-opiocortin peptides in rat cerebrospinal fluid.

Cerebrospinal fluid (CSF) taken from rats implanted with chronic cisternal cannulae was subjected to gel filtration chromatography on Sephadex G-50. Fractions were monitored using radioimmunoassays for N-terminal pro-opiocortin (N-POC), gamma 3-melanotropin (gamma 3-MSH), C-terminal adrenocorticotropin (C-ACTH), alpha-endorphin, beta-endorphin, gamma-lipotropin (gamma-LPH) and alpha-MSH. Two peaks which corresponded in elution position to rat N-POC (1-74) and gamma 3-MSH were detected. The major C-ACTH-immunoreactive (IR) peak was found to correspond to 14k ACTH. While no alpha-endorphin immunoreactivity was detected in rat CSF, three beta-endorphin-IR peaks were identified in positions expected for beta-LPH, beta-endorphin (1-31) and beta-endorphin (1-27), as well as a major peak of activity with the elution characteristics and cross-reactivity of rat gamma-LPH. HPLC of the alpha-MSH-IR material in rat CSF revealed the presence of a major peak of immunoreactivity whose retention time did not correspond to the known oxidised and reduced forms of alpha-MSH and its desacetylated and diacetylated derivatives. The identity of this peak is unknown.

Adrenocorticotropic Hormone↗
PubMed1985

Lymphocytotoxic antibodies in leukemic patients treated with bone marrow transplantation.

Lymphocytotoxic antibodies were studied sequentially in a series of 42 patients with leukemia who received a bone marrow graft. Of these patients, 38% had cytotoxic antibodies before bone marrow transplantation (BMT). After BMT the antibody status changed with time, but 62% of the patients had antibodies at some time after BMT. During the first 10 weeks after BMT, 40% of the patients had antibodies. Thereafter the frequency rose to 50% and remained at that level beyond one year after BMT. In successful grafts the gamma globulins are of donor origin six months after BMT; thus donor B cells are capable of forming lymphocytotoxic antibodies even when the immune system is suppressed by cyclosporine. The antibodies had recognizable HLA specificity in about half the cases before and after BMT. When donor and patient were HLA-identical, HLA specificity did not correspond to donor/recipient antigens. In two cases in which the donor was matched for only one haplotype, antibodies formed by recipient cells, active against donor HLA antigens, were found.

Antilymphocyte Serum↗
PubMed1984

Growth hormone releasing factor (GRF) immunoreactivity in human and rat gastrointestinal tract and pancreas.

Rabbit antisera were raised against a synthetic growth hormone releasing factor, which was originally isolated from a human pancreatic endocrine tumor (hpGRF-44). The antisera obtained showed no significant cross-reactivity with a variety of neurohormonal peptides. In addition to its occurrence in the human, but not in the rat, hypothalamus, hpGRF-44-like immunoreactivity was identified in human gastric antrum and human as well as rat pancreatic islets, using an indirect immunoperoxidase technique. Staining of serial sections and double staining revealed that in the gastric antrum the immunoreactivity was largely confined to gastrin (G) cells, whereas in pancreatic islets polypeptide (pp) cells were reactive. The physiological significance of these findings remains to be established.

Animals↗
PubMed1984

Influence of basic and branched chain amino acid interactions on the lysine and valine requirements of young turkeys.

Two experiments were conducted to determine the influence of amino acid interactions on the lysine and valine adequacy of a low protein diet fed to Large White turkeys from 7 to 19 days of age. Corn-soybean meal diets containing 22 and 30% protein served as controls in both experiments. Test diets involved supplementation of the 22% protein diet with several essential amino acid mixtures. Each diet was fed ad libitum to two pens of eight males and two pens of eight females in each of three trials, except that the 22% protein control diet was fed to four and two pens of each sex per trial in Experiments 1 and 2, respectively. Experiment 1 varied the levels of lysine (0, .60, and 1.20%) and arginine (0, .64, and 1.28%) included in the amino acid mixture. A decrease in supplemental lysine from .60 to 0% reduced weight gain and feed efficiency by 8.6 and 2.4%, respectively. The lysine deficiency was not exacerbated by arginine supplementation up to 179% of the requirement. The effects of altering the leucine (0, .54, and 1.08%) and isoleucine (0 and .4%) contents of the amino acid mixture on the valine requirement were investigated in Experiment 2. Leucine and isoleucine supplementation of diets containing 1.25% valine acted independently to reduce weight gain and feed intake, but the depressions were reversed with the addition of .44% valine. Maximum weight gain and feed efficiency were not achieved with diets containing 1.25% valine and no added leucine or isoleucine, which were indicative of a true valine deficiency in the basal 22% protein diet.(ABSTRACT TRUNCATED AT 250 WORDS)

Amino Acids↗
PubMed1984

A rabbit helper T cell clone reactive against group-specific streptococcal carbohydrate.

Cloned rabbit T cell lines specific for the group-specific carbohydrate of group C streptococcus were established to study T cell responses to this antigen. T cell lines and clones of these lines were prepared from peripheral blood lymphoid cells of animals previously hyperimmunized with group C streptococcal vaccine. All cell lines studied were antigen specific in that they proliferated in the presence of group C but not group A vaccine. Three clones from one rabbit showed strong proliferation in the presence of soluble group C carbohydrate, in addition to the particulate vaccine. One of these clones, 5317.1, upon additional characterization, was shown to possess helper activity in that it induced autologous B cells to produce anti-carbohydrate antibody. Interestingly, B cells could not be stimulated by this carbohydrate-responsive clone to produce anti-carbohydrate antibody in the presence of soluble carbohydrate; the intact vaccine was required to demonstrate the helper effect of the clone. Phenotypic characterization of this clone with a panel of monoclonal antibodies indicated that it was of the T1 subpopulation of peripheral T cells. No suppressor activity was observed for any of the lines studied. Although the use of outbred animals in T cell cloning experiments has certain disadvantages, the present results indicate that cloned rabbit T cells may be useful tools for the elucidation of phenotypic and functional differences of rabbit T cell subsets.

Animals↗
PubMed1983

Endorphin-related peptides in rat cerebrospinal fluid.

Cerebrospinal fluid (CSF) samples were taken from rats implanted with chronic cisternal cannulae and assayed for methionine-enkephalin, beta-endorphin and corticotropin (ACTH). Immobilization stress had little apparent effect on immunoreactive levels of the peptides in the CSF. Gel chromatographic analysis of the beta-endorphin- and ACTH-immunoreactive profiles in rat CSF revealed several peaks. beta-Endorphin-immunoreactive peaks were present at the expected positions of pro-opiocortin, beta-lipotropin and beta-endorphin. ACTH-immunoreactive peaks eluted at positions corresponding to pro-opiocortin, the 20-23K ACTH biosynthetic intermediate, 14K ACTH, and 4.5K ACTH. These results suggest that rat CSF contains peptides of the pro-opiocortin family similar to those previously described in rat pituitary.

Adrenocorticotropic Hormone↗
PubMed1983

Isolation and characterisation of genomic and cDNA clones for an androgen-regulated secretory protein of rat seminal vesicles.

Testosterone controls the synthesis of seminal vesicle protein F in male rats by regulating the cellular concentration of its mRNA (mRNAF). Phage lambda recombinants have been isolated containing the complete F gene. In addition plasmids have been constructed containing cDNAF sequences some of which are probably full-length (approximately 700 bp). Detailed restriction mapping shows that the F gene is 1.7 kbp long and contains approximately 1.0 kbp of intervening sequence arranged in at least two introns (420 bp and 600 bp). Part of cDNAF has been sequenced showing that the terminal 125 bp of the 3' untranslated region of mRNAF has substantial (greater than 70%) sequence homology with the 3' end of the mRNA coding for another androgen-dependent seminal vesicle protein (protein S). The cloned F gene has been detected in liver and seminal vesicle DNA along with an homologous but structurally different gene. The hormonal control of mRNAF was examined with cDNAF. A pronounced (approximately 3000-fold) differential response to testosterone was observed.

Androgen-Binding Protein↗
PubMed1983

Differentiation antigens identify subpopulations of rabbit T and B lymphocytes. Definition by flow cytometry.

A panel of six monoclonal antibodies produced against cell surface glycoproteins of a rabbit T lymphocyte line was used with flow cytometry to define rabbit lymphocyte subpopulations. Four thymocyte populations were characterized by size and expression of cell surface antigens and appear to represent stages in thymocyte differentiation. Rabbit spleen contained five subpopulations: two of T lineage, two of B, and a null cell subset. Bimodal distribution of staining of thymocytes and peripheral T cells was observed using an antibody (9AE10) directed against a Thy-1 analogue in the rabbit, suggesting two separate T cell lineages. One of the monoclonal reagents, L11/135, reacted strongly with peripheral rabbit T cells as shown by two-color immunofluorescence. In functional studies, only the L11/135-bearing cells responded to the T cell mitogens concanavalin A and phytohemagglutinin and to allogeneic splenocytes. The thymocyte subpopulations and the peripheral T and B cell subsets differ from those described in mouse and man.

Animals↗
PubMed1983

Long lived nonadherent rabbit macrophages obtained from spleen cell cultures.

During the preparation of rabbit-mouse hybridomas, an unusual degree of cellular proliferation and a high level of rabbit immunoglobulin secretion in culture was noted. The proliferation seemed to be dependent on the use of relatively high levels (10%) of fetal bovine serum because it was not seen when spleen cells were cultured using either horse serum or autologous serum in a variety of media. The peak of the proliferative response occurs at 7 to 10 d in culture, after which the lymphoblast population dies rapidly, leaving a large, granular, nonadherent cell as the predominant component in the culture. These cells did not seem to divide further but persisted in very gradually diminishing numbers for many months. This long lived cell has been characterized as a nonadherent macrophage by its morphology, intense esterase staining, expression of an Fc receptor for rabbit IgG, phagocytosis of latex particles and opsonized sheep erythrocytes, and mediation of antibody dependent cell mediated cytotoxicity on chicken erythrocytes.

Animals↗
PubMed1983

The role of rabbit immunoglobulin allotypes in an immune network.

The expression of latent allotypes is a well documented phenomenon in rabbits. Speculation about their molecular genetic basis and the mechanisms that control expression of these unexpected markers lead inevitably to questions about the Ig gene complement of the rabbit. This central question is under current study using probes derived originally from the mRNA of rabbit-mouse hybridomas secreting rabbit Ig chains. Some of the basic features of rabbit Ig genes are already clear from these studies, and DNA fragments that might encode latent allotypes have been identified with the first set of probes. Further gene closing sequencing should shortly provide a definitive answer to the question of latent allotypy and will also provide a detailed understanding of nominal Ig expression in rabbits.

Amino Acid Sequence↗
PubMed1983

Secretion of pro-opiocortin peptides from isolated perfused rat pars intermedia cells.

The perfused, isolated, pituitary cell column was used to measure the release of alpha-melanotropin (alpha-MSH)-like immunoreactivity (LI), carboxyl terminal corticotropin (C-ACTH)-LI, gamma-lipotropin (gamma-LPH)-LI, alpha-endorphin-LI, beta-endorphin-LI and amino-terminal pro-opiocortin (N-POC)-LI from rat pars intermedia (PI) cells. Concomitant secretion of all PI peptides was observed during basal release and in response to all applied stimuli. Dopamine (DA) caused a dose-dependent (10(-9)-10(-5) M) simultaneous inhibition of peptide release which was antagonised by haloperidol. Isoprenaline stimulated the release of PI peptides in a parallel, dose-related (10(-10)-10(-6) M) manner and was blocked by propranolol. Stimulation of peptide secretion caused by low concentrations (10(-8) M), of adrenaline (AD) and noradrenaline (NA) changed to inhibition at high concentrations (10(-5) M) whereas intermediate concentrations (10(-6), 10(-7) M) possessed both inhibitory and excitatory effects. A 45 mM solution of K+ ions stimulated the release of PI peptides and both the K+-stimulated secretion and basal secretion were Ca++-dependent. MSH-release-inhibiting factor (MIF) and 5-hydroxytryptamine (5-HT) failed to alter peptide secretion from the perfused PI cells. We conclude that pro-opiocortin (POC) peptides are released concomitantly from rat PI cells and that biogenic amines are involved in their release.

Adrenocorticotropic Hormone↗