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Biomedical subjects

C Penel

Publications and source records attributed to C Penel.

51 records · Page 3Linked to original sources

Thyroid morphological and functional heterogeneity: impact on iodine secretion.

Thyroid iodine turnover heterogeneity includes morphological (cellular and colloidal distribution space for iodide) and functional heterogeneity (hormone synthesis in the colloid). In 'normal' rats, both iodide actively trapped by the epithelial cell and that coming from deiodination of iodotyrosines present the same probability for thyroglobulin (Tg) iodination (Tg iodination flux: 4.0 +/- 0.3 micrograms I/day). A portion of the thyroid iodide is sequestered in the colloid lumen and is inoperative in the Tg iodination mechanisms. The masses of cell and colloid compartments are equivalent (0.018 +/- 0.002 micrograms I) while colloid iodide concentration is twice that of the cell (0.11 and 0.06, respectively). The turnover of about 3 micrograms I of colloid iodine (Tg) is follicle diameter-dependent (inter-follicular heterogeneity) and it is mainly characterized by 2 different half lives of 8 and 16 hours, respectively. Ninety percent of the thyroid iodine (hormone) secretion (1.10 +/- 0.11 micrograms I/day) is provided by this compartment rich in iodotyrosine residues (70%). The remaining 10% of iodine secretion is provided by a Tg pool (7 micrograms I) characterized by 2 compartments (intra-follicular heterogeneity) with slow and very slow turnovers. The longer the transit time of Tg molecules in the colloid, the higher their iodothyronine content.

Animals↗

Peroxidase Release Induced by Ozone in Sedum album Leaves: Involvement of Ca.

The effect of ozone was studied on the peroxidase activity from various compartments of Sedum album leaves (epidermis, intercellular fluid, residual cell material, and total cell material). The greatest increase following a 2-hour ozone exposure (0.4 microliters O(3) per liter) was observed in extracellular peroxidases. Most of the main bands of peroxidase activity separated by isoelectric focusing exhibited an increase upon exposure to ozone. Incubation experiments with isolated peeled or unpeeled leaves showed that leaves from ozone-treated plants release much more peroxidases in the medium than untreated leaves. The withdrawal of Ca(2+) ions reduced the level of extracellular peroxidase activity either in whole plants or in incubation experiments. This reduction and the activation obtained after addition of Ca(2+) resulted from a direct requirement of Ca(2+) by the enzyme and from an effect of Ca(2+) on peroxidase secretion. The ionophore A23187 promoted an increase of extracellular peroxidase activity only in untreated plants. The release of peroxidases by untreated and ozone-treated leaves is considerably lowered by metabolic inhibitors (3-(3,4-dichlorophenyl)-1,1-dimethylurea and sodium azide) and by puromycin.

Journal Article↗

Vascularization and iodide transport down regulation in rat goitre.

This study was designed to investigate, in the rat, the regulation of the amount of thyroid iodide and of its organification during the involution of an experimentally induced goitre. The goitre was obtained by drastic iodine deficiency; male Wistar rats received an iodide deficient diet for 6 months, supplemented with PTU during the last 2 months. The study was followed for 16 days after the beginning of iodide refeeding (daily iodine intake = 50 micrograms). The thyroid iodide, total thyroid organic iodine and plasma iodide, PBI and TSH concentrations were determined from day 0 to 16 and compared to their control values (rats on a normal iodide diet for 6 months). In addition, a stereological study was carried out to determine if the extent of the gland vasculature might be implicated in the regulation of the thyroid iodide content. The plasma TSH concentration was very high and constant for 8 days (2.40 +/- 0.37 and 2.45 +/- 0.43 on day 0 and 8 respectively vs 0.25 +/- 0.12 microgram/ml in control rats), whereas iodination and secretion were blocked for 4 days (0.34 +/- 0.19 and 0.5 +/- 0.1 on day 0 and 4 respectively vs 14.4 +/- 2.0 micrograms 127I/gland in control rats) (Wolff-Chaikoff effect). Thyroid iodide amount increased enormously for 2 days (2.5 +/- 0.6 and 2.45 +/- 0.55 respectively on day 1 and 2 vs 0.09 +/- 0.01 micrograms 127I/gland on day 0), then strongly decreased between 2 and 4 days (1.15 +/- 0.27 127I/gland).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Distribution of calmodulin-stimulated ca transport into membrane vesicles from green spinach leaves.

A microsomal fraction isolated from green spinach leaves exhibited a Mg(2+) and ATP-dependent (45)Ca(2+) uptake. Addition of 10 micromolar carbonyl cyanide m-chlorophenylhydrazine had no effect. The cationophore A23187 (10 micromolar) induced the release of (45)Ca(2+) accumulated by membrane vesicles. Membranes prepared from lower epidermis showed the highest Ca(2+) accumulation activity. Microsomal fractions from petiole, lamina, and midrib were less active. The stimulation by bovine brain calmodulin was about 30% for the lower epidermis, 23.5% for midrib, and below 20% for petiole and lamina.

Journal Article↗

Thyrotropin effects on vesicle transfer and thyroid follicle morphogenesis: a stereological study in the rat.

Incubation in a culture medium with and without TSH of 16 day-old foetal thyroid glands induces hypertrophy of the Golgi apparatus which may be correlated with a considerable increase in the number of secretory vesicles. A stereological study performed during the first 6 hr of incubation showed that: vesicle secretion was biphasic; vesicle secretion was heterogeneous with two different populations of vesicles; When TSH (20 mU and 80 mU) was added to the medium, the volume density of the follicular lumina increased; at least during the first 6 hr TSH seemed to be necessary to the formation of follicular lumina.

Animals↗

Correlation between thyroid-follicle fusion and structural modifications of the epithelial cells. A quantitative study in the adult rat.

Changes in thyroid structure induced by a decrease in TSH or iodide-dependent stimulation were quantified by stereological analysis of light micrographs. Studies were carried out on intact (R5) and hypophysectomized (R5H) rats receiving 5 micrograms iodide, and on intact rats (R5O) receiving 50 micrograms iodide daily. For R5H- and R5O-thyroids, the mean parameters of the epithelial cells, height, volume and lateral membrane area, were smaller than those of R5-thyroids. An inverse shift was observed for the apical membrane area, whereas the peripheral membrane area was unchanged. The number of epithelial cells was similar in each of the three groups; however, the number of follicles was greater in R5-thyroids, suggesting that follicular fusion occurs in R5O- and R5H-thyroids. This was confirmed by direct observation. The present results demonstrate that in adult rats a lack of TSH or an increased iodide diet (insufficient to produce a physiopathological state) induce follicle fusion probably by means of cellular reorganization. This increase in follicle size could be involved in the regulation of thyroid iodine turnover.

Animals↗

Rapid Correlation between the Leaves of Spinach and the Photocontrol of a Peroxidase Activity.

The activity of a basic peroxidase extracted at high pH from spinach (Spinacia oleracea) leaves is modified by an irradiation with 2-minute red light or 2-minute far red light. This fast response, apparently mediated by phytochrome, is also detected in other leaves darkened with black paper. It is proposed that some fast signal moves from irradiated to darkened leaves. This signal, but not the direct control of peroxidase activity in irradiated leaves, is suppressed by inhibitors known for their effect on Na(+) or K(+) distribution (ouabain, lithium, tetrodotoxin, tetraethylammonium). Substances affecting Ca(2+) distribution inhibit both the signal transmission and the direct photocontrol of peroxidase activity.

Journal Article↗

Calcium requirement for the secretion of peroxidases by plant cell suspensions.

Spinach (Spinacia oleracea, L.) cells in liquid culture release peroxidases. This release is reduced by EGTA and promoted by calcium ions. In a medium deprived of calcium the rate of peroxidase release is low, but immediately after addition of I mM calcium there is a sudden increase of the extracellular peroxidase activity. Extracellular calcium apparently penetrates into the cultured cells rather freely and, as a consequence, the rate of peroxidase secretion by these cells is directly correlated with the concentration of calcium in the medium. Magnesium, at twice the concentration used for calcium, has no effect on the release of peroxidases. Cells treated with Na azide, Na hydrogenarsenate of fluphenazine secrete less peroxidase upon addition of calcium.

Calcium↗

Intrafollicular re-cycling of organic iodine in the hypophysectomized rat as observed by a long-term kinetic study.

A long-term kinetic study was started 8 days after hypophysectomy in rats previously adapted to receive 5 micrograms iodide daily, and maintained on the same diet after surgery. At each time, the renewed fraction for thyroglobulin (Tg) and lysosomes in the gland, and hormones in the plasma was calculated by the method of isotropic equilibrium. All the pools studied are renewed very slowly, but with different kinetics. Between time zero and the 25th day of the experiment, the renewed fraction in plasma hormones always exceeds that of Tg. Thus, in hypophysectomized rats, Tg pool is composed of at least two compartments with different turn-over rates. Tg molecules of both compartments are endocytosed, but that of the faster compartment participate in secretion in a preferential way. Peeling of the data for the 60-day period of experiment confirms these results. In addition, peeling demonstrates a 15-day delay in the turn-over of the second compartment. Such a delay was not found in the turn-over of this compartment in lysosomes. Thus, we may again postulate, in hypophysectomized rats, a recycling of iodine in organic form from the lysosomes back to the luminal colloid, as previously porposed for control rats.

Animals↗

[Peroxidases of high molecular weight identified as the membrane peroxidases in lentils].

Peroxidases extracted from lentil roots are separated in two peaks by gel chromatography on Sephadex G-100 or on Bio Gel A-5 M. On both resins, the first peak of extremely large molecular weight is demonstrated to be an association of some peroxidases with microsomes. These enzymes can be detached from membranes by NaCl. Starch gel electrophoresis shows that isoperoxidases associated electrostatically to microsomes are basic peroxidases apparently not different from those of the soluble fraction.

Cell Membrane↗