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J Roche

Publications and source records attributed to J Roche.

At least 109 records · Page 6Linked to original sources

[Endogenous opiate modulators of insulin secretion in the obese].

The effects of endogenous opiates on insulin response to oral glucose load were studied in obese subjects and in lean healthy volunteers. None of these having a family diabetes. After 3 days on an 1,800 cal./m2, 40% carbohydrate diet all subjects underwent two standard 75 g oral glucose tolerance tests (OGTT), one of which was accompanied by an i. v. administration of 10 mg of, an antagonist of opiates, the naloxone. In one group of obese impaired oral glucose tolerance test occurred. All obese, but not the lean healthy volunteers, showed: 1) increased basal plasma insulin levels, 2) higher insulin response to OGTT, 3) a decrease in insulin response to OGTT after naloxone administration, with significant differences at 60 min (p less than 0.01) and 90 min (p less than 0.025). In none of the subjects significant differences were observed in blood glucose levels after OGTT plus naloxone administration. These data suggest that increased endogenous opiates may affect insulin response to glucose in obese with impaired or normal oral glucose tolerance test. At present there seems to be no satisfactory explanation for unchanged blood glucose levels during OGTT with and without naloxone despite a decrease in insulin secretion in the obese patients.

Adolescent↗

Pharmacokinetics of 111In-labeled OC-125 antibody in cancer patients compared with the 19-9 antibody.

We recently reported on the pharmacokinetics in 14 cancer patients of the 19-9 antibody radiolabeled with 111In. We have now repeated this investigation in 18 cancer patients using the OC-125 antibody, in part to compare the in vivo behavior of two murine monoclonal antibodies of the same subclass administered as the F(ab')2 fragments, by the same route and at the same dose. As in the earlier investigation, 1 mg of fragments was infused i.v., and organ quantitation was obtained for up to 72 h along with frequent blood and urine samples for chromatographic evaluation. Analysis of urine showed that activity clearance by this route amounted to 0.29%/h and consisted of labeled DTPA only in early samples and metabolic products thereafter. Analysis of serum samples often showed the presence of a high-molecular-weight species appearing within 24 h. This species is probably due to antibody binding to circulating antigen, although the percentage of circulating activity present as this species did not correlate well with circulating antigen levels. As before, organ accumulation was greatest in the liver, although levels were significantly reduced (12% compared to 20% of administered dose at 24 h, P less than 0.01). Plasma clearance was also significantly different: whereas the label in the case of the OC-125 antibody showed one-compartment clearance kinetics and remained in the plasma compartment, in the 19-9 case the label diffused to a second, unidentified compartment.

Antibodies, Monoclonal↗

Is there a place for forearm osteodensitometry in clinical screening studies?

In order to evaluate forearm osteodensitometry for its potential to detect subjects with a low spinal mineral content and/or vertebral fractures, single-photon absorptiometry of the forearm and estimations of spinal mineral content by computed tomography were performed in 124 normal and abnormal subjects. Eighty-one per cent (22/27) of patients with vertebral crush fractures had a low spinal mineral content. In contrast, among 64 apparently normal individuals, six patients (four women, two men; 9.4%) had a low spinal mineral content. Forearm osteodensitometry showed a significant positive correlation with spinal mineral content. A forearm value in women in excess of 35 arbitrary units was associated with a spinal value of 75.1-mg equivalent dipotassium phosphate (K2HPO4) or above in 29/31 cases. A forearm value in women of 28.5 arbitrary units or lower was associated with a spinal value of 75-mg equivalent K2HPO4 or less in 20/24 subjects. While of no predictive value for the spine in patients with intermediate readings, forearm osteodensitometry is nevertheless considered a useful screening procedure for spinal osteoporosis.

Adult↗

[Fluorescent properties of (Na+/K+)ATPase].

1. The effect of ouabain on the molecular properties of (Na+/K+)-ATPase has been studied in purified preparations of the enzyme, isolated from the microsomal fraction of outer red medulla of porcine kidney, according to a modification of the method described by Jorgensen. 2. Ouabain, a specific inhibitor of (Na+/K+)-ATPase, binds at the potassium site of the enzyme, thus generating an increase in its stability towards the common denaturing agents, such as exposure to different concentration of guanidinium chloride (GdmC1) or to acidic solutions.

Animals↗

[Changes in the ratio of T-lymphocyte subpopulations in various cytological samples of Plummer's thyroid adenoma].

UNLABELLED: In order to correlate possible alterations of cell-mediated immune response with the evolutive phases of Plummer Adenoma (P. A.), T lymphocytes subpopulations in FNA samples and in peripheral blood lymphocytes (PBL) have been studied in 5 patients with autonomous nodules. The lymphocyte component in FNA and peripheral blood has been isolated by Lymphoprep gradient centrifugation; the analysis of T helper and T suppressor subpopulations was made by indirect immunofluorescence with OKT8 and OKT4 monoclonal antibodies. Our results show a reduction in OKT4/OKT8 ratio in cytological samples compared with PBL in patients with P. A., while in control subjects there was not statistically significant difference. In the patients with P. A., the relative increase of OKT8 lymphocytes in FNA compared with PBL is correlated with the functional state, that is toxic adenomas have a lower OKT4/OKT8 ratio compared with nodules in pre-toxic phase. IN CONCLUSION: T lymphocyte subpopulations typing in FNA demonstrate that, even in this type of hyperthyroidism, immune response disorders are present and consist of relative increase of suppressor/cytotoxic T cells, compared to T helper cells.

Adenoma↗

Effect of amplitude-modulated 147 MHz radiofrequency radiation on calcium ion efflux from avian brain tissue.

Cerebral cortex tissue slices and cerebral hemispheres prepared from Gallus domesticus chicks were exposed to 147 MHz radiofrequency radiation, amplitude modulated at 16 Hz and applied at a power density of 0.75 mW/cm2, to determine the effect of such exposure of 45Ca2+ efflux from the avian brain tissue. Statistical analysis of these data demonstrates that such exposure has no significant effect on 45Ca2+ efflux.

Animals↗

[Effects of enzymatic deglycosylation of human goiter thyroglobulin on its immunochemical properties].

Thyroglobulin (Tg), isolated from soluble iodoproteins by ammonium sulphate fractionation, was enzymatically deglycosylated in vitro and analyzed by polyacrylamide gel electrophoresis, double immunodiffusion and non-commercial RIA. Carbohydrate and iodine content was chemically determined. By PAAGE deglycosylated Tg (dTg) showed the appearance of a major band in the 12S region and three slower migrating bands corresponding to higher aggregates than 19S Tg. In immunodiffusion by testing native and deglycosylated Tg against anti-native Tg antiserum it was shown the appearance of a spur of native on deglycosylated Tg. By RIA of native and deglycosylated Tg against anti-deglycosylated Tg antiserum it was shown a minor binding capacity of the anti-deglycosylated antibody against native Tg at high dilutions. The results demonstrate that the enzymatic deglycosylation release almost all the carbohydrates of goiter Tg and that the removal of the carbohydrates of Tg produces a loss of antigenic determinants of the molecule.

Electrophoresis, Polyacrylamide Gel↗

[Polymorphism of human thyroxine binding serum globulin (TBG); existence of a new form of serum protein without detectable triiodothyronine binding power].

Two kinds of TBG polymorphism are described in human, one found in deglycosylated TBG from individual blood donors, the other is a genetically determined polymorphism. TBG from plasma samples from a patient with toxic goiter, not autoimmune, (p)TBG, from the patient's mother (m)TBG and from individual donors (n)TBG, were labeled with [125I]T4 or [125I]T3 and submitted to isoelectric focusing (IEF), followed by autoradiography. Three faint [125I]T4 radiolabeled bands were detectable in (p)TBG while four strong [125I]T4 radiolabeled bands were detectable in (m)TBG and (n)TBG), respectively. IEF of the [125I]T3 incubated serum samples resulted in no detectable isoelectric radiolabeled band for (p)TBG while a normal pattern was found in (m)TBG and in (n)TBG, respectively. These data suggest a new intraindividual not linked to sexual chromosome X polymorphism characterized by a loss in hormone binding.

Adult↗

Differences in the condensation of chromatin by individual subfractions of histone H1: implications for the role of H1(0) in the structural organization of chromatin.

The effectiveness of histone H1 subfractions H1-1 and H1(0) in inducing the ordered condensation of chromatin was examined by thermal denaturation, circular dichroism, electric birefringence, orientation mechanism, and orientational relaxation time measurements. Soluble rat liver chromatin was stripped of H1 by dissociation in 500 mM NaCl and long fragments of chromatin were subsequently reassociated with purified individual H1 subfractions for ratios of 1 and 2 mol of H1 per nucleosome. H1 subfractions behave differently with respect to their interactions with DNA in chromatin: although the orientation mechanisms of reconstituted chromatins are identical, H1(0) induces a less efficient protection of DNA than H1-1, as shown by nuclease digestion and by the length of free extended linker DNA determined by electric birefringence. This corresponds to a more extended structure of H1(0)-reconstituted chromatin as judged by the value of relaxation time. One can imagine that the replacement of H1 by H1(0) leads to a different structure or stability of the chromatin, confering a certain degree of flexibility of this region. This may be related to the functional role of H1(0) in DNA replication or transcription and may explain metabolic and evolutionary differences among H1 subfractions as recently suggested by Lennox [Lennox, R. W. (1984) J. Biol. Chem. 259, 669-672]. The extent of condensation when H1-depleted chromatin is overloaded with histones is probably a function of the electrostatic interactions between the basic C-terminal tails of histones and chromatin. Electric birefringence also reveals differences between native and reconstituted chromatins that are overlooked by several other criteria.

Animals↗

The involvement of histone H1[0] in chromatin structure.

Micrococcal nuclease digestion and light scattering are used to compare native chromatins with various histone H1[0] contents. The experimental data show that the higher the H1[0] content, the greater the ability to form compact structures with increasing ionic strength, and the lower the DNA accessibility to micrococcal nuclease. On the contrary, reconstituted samples from H1-depleted chromatin and pure individual H1 fractions behave in such a way that samples reconstituted with pure H1 degree give rise to a looser structure, more accessible to nuclease than samples reconstituted with H1-1. This contradiction suggests that the effect of H1o on chromatin structure must originate from the interaction of this histone with other components in native chromatin among which other histone H1 subfractions are good candidates.

Animals↗