[The legal management of cosmetic surgery complications].
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Cosmetic Techniques↗
Biomedical subjects
A Porte
Publications and source records attributed to A Porte.
[Constitutional anomalies of hemostasis and management in surgical situation. Evaluation of 10 years' activity at the Hospital Centers of Aulnay-sous-Bois and Saint-Denis].
A ten-year retrospective study was conducted in 4 women in labor and 23 surgical patients with congenital clotting factor deficiency. Appropriate use of replacement therapy and good cooperation between biologists, anesthesiologists, and surgeons are essential to ensure a favorable outcome.
Adolescent↗
Early bronchopulmonary lesions in rat lung after normobaric 100% oxygen exposure and their evolution. A light and electron microscopic study.
In order to clarify the early phenomena involved in the lung reaction to hyperoxia, twenty adult male rats were exposed to 100% oxygen at 1 ATA. Morphological pulmonary lesions were detectable after only 24 h hyperoxia, and included vasoconstriction and perivascular oedema, bronchiolar constriction, and pericyte reaction. The lesions were irregularly scattered within the lung parenchyma and occurred preferentially in areas centred on bronchiolo-vascular stems. Even at the latest stages, pulmonary heterogeneity was obvious, from the coexistence of areas damaged at different times. Neuro-epithelial-bodies were found under the bronchiolar epithelium; the morphological aspect of the neuro-endocrine cells observed was consistent with hyperoxia-induced modulation of their secretory activity. Taken together, our findings show the speed of development of hyperoxia-induced pulmonary changes and raise some pathogenic considerations.
Animals↗
Pharmacological characteristics and anatomical distribution of [3H]oxytocin-binding sites in the Wistar rat brain studied by autoradiography.
Oxytocin-binding sites were detected by autoradiography on rat brain sections incubated in the presence of the [3H]oxytocin. These sites were characterized pharmacologically using quantitative autoradiography. High pressure liquid chromatography controls of the incubation media indicated that labelling was due to the intact [3H]oxytocin molecule. Pharmacological analysis of different locations (central amygdaloid nucleus, ventral subiculum and ventromedial hypothalamic nucleus) showed that the sites detected had a high affinity for oxytocin and also for arginine-vasopressin. In contrast, some areas known to bind vasopressin intensely, such as suprachiasmatic and lateral septum nuclei, had little or no affinity for oxytocin. Autoradiographs revealed [3H]oxytocin-binding sites in already known brain areas (olfactory centres, ventral subiculum, central amygdaloid nucleus, bed nucleus of the stria terminalis) albeit with more extensive labelling of some of these formations, in particular, the amygdaloid complex. In addition, specific [3H]oxytocin-binding sites were found in areas not yet reported to bind oxytocin, such as the paraventricular thalamic and caudate nuclei. In the hypothalamus, specific binding sites were not detected in the supraoptic and paraventricular nuclei: the only structure labelled was the ventrolateral part of the ventromedial nucleus. Discrepancies between the concentrations of [3H]oxytocin-binding sites, the known distribution of oxytocin-containing endings and electrophysiological data indicate that autoradiography, under our conditions, apparently only reveals some of the oxytocin receptors in the brain. Thus, in the hypothalamus, no relationship can be established between the known effect of oxytocin on oxytocinergic magnocellular neurons and detection of specific [3H]oxytocin-binding sites. Autoradiography may reveal mainly oxytocin-binding sites in areas receiving diverse "parasynaptic" information, where oxytocin might play a modulatory role rather than exerting rapid, short-term effects of the neurotransmitter type.
Amygdala↗
Autoradiographic localization of binding sites for oxytocin and vasopressin in the rat kidney.
The distribution of [3H]vasopressin- and [3H]oxytocin-binding sites was examined, using an autoradiographical technique, in the kidney of Long-Evans and Brattleboro rats. Two types of binding sites with affinities in the nanomolar range were detected: one, located on glomeruli, bound both vasopressin and oxytocin; the other, on collecting ducts, bound vasopressin selectively. In the presence of 10 mumol oxytocin/l, [3H]vasopressin labelling was abolished in glomeruli, but only reduced in collecting ducts; [3H]oxytocin labelling was completely abolished by 10 mumol vasopressin/l. These observations are discussed in relation to known effects of neurohypophysial hormones on renal physiology.
Animals↗
Light and electron microscopic structure of the cardiac Purkinje fibers--review.
The history and the morphological characteristics of the Purkinje fibers are reviewed briefly in different species and in the atrioventricular (A-V) bundle branches (BB) of the same species. The so-called typical Purkinje fibers corresponding to the original description are found in birds, ungulates, and larger mammals. The specialized fibers of the ventricular impulse conduction are present, however, in all mammals and are distinguishable with new and reviewed morphological methods from the force-producing fibers. The Purkinje fiber term is applicable for all the BB fibers, which, by their morphology, might be classified in man and small mammals as Purkinje I (proximal BB), II (ramified BB), and III (terminal) fibers. The main characteristics of the Purkinje fibers are: cable-like structure in birds, ungulates, and proximal BB fibers of other mammals; lack of transverse tubular system; generally little contractile material associated with a high number of intermediate filaments; few mitochondria and low mitochondrial enzyme activity; high amount of glycogen and anaerobic ability rendering them relatively resistant to hypoxia. The distribution of the Purkinje net-work and the modes of Purkinje and ventricular fiber interconnections are also reviewed.
Animals↗
[Sheehan's syndrome (acute steatosis of the liver in pregnancy). Apropos of 8 cases].
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Acute Disease↗
Dopamine D2 receptors are restricted to the prolactin cells in the rabbit pituitary gland: a combined autoradiographic and immunocytochemical study.
The distribution of dopamine D2 receptors was studied using the autoradiographic technique on rabbit pituitary gland sections incubated in the presence of [3H]spiroperidol. D2 receptors were absent from the intermediate lobe as already reported. In the anterior lobe, the location of D2 receptors exactly overlapped that of the prolactin-producing cells revealed by immunocytochemistry on the sections used for autoradiography. No topographical relationships could be found between the D2 receptors and the TSH-producing cells which are known to be inhibited by dopamine in the rat.
Animals↗
Absence of inhibitory dopaminergic control of the rabbit pituitary gland intermediate lobe.
No immunoreactive axons were detected with an antiserum against tyrosine hydroxylase in the rabbit intermediate lobe (IL), which thus appears to be devoid of dopaminergic (DA) innervation. Dopamine and its agonists, which classically inhibit alpha-MSH release have no inhibitory effects on rabbit IL superfused in vitro but, paradoxically, stimulate alpha-MSH release. D2 type DA receptors, known to mediate inhibitory control of dopamine on melanotropic cells, and detectable by their affinity for (3H)-spiroperidol, were as previously reported absent from the rabbit IL. The absence of (3H)-spiroperidol binding sites in the IL was further confirmed on rabbit pituitary sections by radioautography. The mechanism of DA stimulation is still not clear, but might be tentatively explained by interference with other receptors involved in the stimulation of the gland. The lack of DA inhibitory control over the rabbit IL is an exception among the species so far studied.
Animals↗
[Corneo-conjunctival pigmentation caused by lamprene].
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Adult↗
Opposite effects of monosodium glutamate on the dopaminergic and GABAergic innervations of the median eminence and the intermediate lobe in the mouse.
In the mouse, monosodium glutamate (MSG) administered neonatally provokes the necrosis of most dopaminergic perikarya in the arcuate nucleus, as classically described, but also stimulates surviving neurons as shown by their increase in both size and immunoreactivity for tyrosine hydroxylase (TH). In the treated animals, TH-immunoreactive axons rarefy in the median eminence (ME) external zone, but postnatal dopaminergic innervation of the intermediate lobe (IL) normally develops and even, due to enlarged axonal varicosities, is more conspicuous than in the control littermate IL at same stages. gamma-Aminobutyric acid-ergic (GABAergic) projections in the ME and the IL, revealed with a glutamic acid decarboxylase antiserum, have the same distribution as TH-immunoreactive axons and present the same modifications in the MSG-treated animals. No clearcut differences in dopaminergic and GABAergic innervation patterns can be observed in the IL in treated and control adult mice.
Animals↗
Immunocytochemical evidence for intragranular processing of pro-opiomelanocortin in the melanotropic cells of the rabbit.
The immunogold technique, employing antisera with clear-cut specificities, was used to localise different processing stages of pro-opiomelanocortin (POMC) in rabbit melanotropic cells. While the antiserum against gamma 3-MSH labelled all the secretory granules including intrasaccular condensations in the Golgi apparatus, antisera against alpha-MSH only labelled extra-Golgi secretory vesicles (SV). All extra-Golgi SV were likewise labelled with the three antisera against alpha-MSH used, despite their different specificities for the deacetylated, N-acetylated or C-amidated forms of the peptide. The antibody against beta-endorphin also labelled the extra-Golgi SV, while only some SV were labelled with the antibody against gamma-endorphin. These results correlate with biochemical data in favour of mainly--if not exclusively--intragranular processing of POMC. Except for gamma 3-MSH, the cleavage of which could coincide with Golgi packaging of secretory material, other post-translational modifications of the precursor seem to occur when SV are discharged outside the Golgi area. The cleavage of gamma-endorphin appears to be a later step in POMC processing, occurring in some mature SV.
Animals↗
[Stimulatory control by oxytocin (or an analog peptide) of the pituitary intermediate lobe in rabbits. Inhibitory role of serotonin].
The peculiar innervation of the intermediate lobe (IL) in Leporidae obviously corresponds to a regulation mechanism different from that known in other mammals. Physiological observations on IL superfused in vitro show, in addition to the previously reported absence of dopaminergic inhibitory control, the existence of an oxytocinergic-like control involved in the stimulation and not in the inhibition of alpha MSH release by the rabbit IL. Serotonine has inhibitory effects and may play a modulatory role. However, the strong stimulation of alpha MSH release obtained with K+ at a depolarizing concentration (8K) suggests that the presence of any powerful inhibitory axonal system in the rabbit IL is rather unlikely.
Animals↗
Cavity designs for composite resins.
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Composite Resins↗
Oxytocinergic neurons with tyrosine hydroxylase-like immunoreactivity in the paraventricular nucleus of the rabbit hypothalamus.
Antiserum against tyrosine hydroxylase clearly reacts with two types of neurons in the rabbit paraventricular nucleus: catecholaminergic neurons, also present in rat and mouse, and neurons also staining for ocytocin and neurophysin; the latter neurons have not been reported in other species. This result raises the question of a possible aminergic potentiality of a subpopulation of oxytocinergic neurons in the rabbit hypothalamus.
Animals↗
Oxytocin-immunoreactive nerve fibers in the pars intermedia of the pituitary in the rabbit and hare.
The pars intermedia of the pituitary in the rabbit and hare is abundantly innervated by axons reacting selectively with antibodies against oxytocin. These axons contain dense secretory vesicles about 140 nm in diameter, i.e., smaller than those in the neurosecretory axons of the neural lobe. No fiber elements staining for other peptides (vasopressin, somatostatin, substance P) were observed in the pars intermedia, except rare leu-enkephalin axons restricted to the rostral zone of the gland. Dopaminergic innervation appears to be completely absent from the intermediate lobe. This was shown by the lack of reaction with an antibody against tyrosine-hydroxylase, which did reveal a well-developed tubero-infundibular system of nerve fibers. Axons reacting with an antibody against serotonin were irregularly distributed in the pars intermedia. In the absence of dopaminergic axons, the extensive oxytocin-like innervation may play a major role in regulating the melanotrophic cell activity in the Leporidae.
Animals↗
Immunocytochemical evidence of intragranular acetylation of alpha-MSH in the melanotrophic cells of the rabbit.
Melanotrophic cells of the pars intermedia of the rabbit were studied at the electron-microscopic level by means of the immuno-gold technique with the use of antisera against gamma 3-MSH and alpha-MSH. Both antibodies labelled all secretory vesicles stored in the peripheral cytoplasm, but secretory vesicles and intrasaccular condensations in the Golgi area reacting for gamma 3-MSH were not labelled with the antibody against alpha-MSH. Since this antibody appears to recognise only the acetylated form of alpha-MSH, the present observations suggest that acetylation occurs at a stage subsequent to the Golgi packaging, during maturation of the secretory vesicles. Thus, the morphological evidence supports biochemical data in favour of intragranular processing of opiomelanocortin in melanotrophic cells.
Acetylation↗
Distribution of immunoreactive fibronectin and collagen (type I, III, IV) in mouse joints. Fibronectin, an essential component of the synovial cavity border.
Hyaluronic acid traditionally has been held to play a major role in the control of transsynovial exchanges and in the biomechanical properties of synovial fluid and cartilage surfaces. As with previous ultrastructural observations, immunohistochemical data show that a more complex differentiation must be envisaged for interstitial tissues bordering the synovial cavity. In particular, the elective concentration of fibronectin in the lining layer of the synovial membrane and its presence as a fine layer at the articular cartilage surfaces indicate that this glycoprotein, along with hyaluronic acid, may play an important role in joint physiology. Only immunoreactivity for type III procollagen is diffusely distributed in the entire synovial membrane and, in addition, is found associated with fibronectin immunoreactivity at the articular cartilage surfaces.
Animals↗