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C Lebrun

Publications and source records attributed to C Lebrun.

98 records · Page 6Linked to original sources

Role of neuropeptides in learning versus performance: focus on vasopressin.

Neuropeptides that have classical hormonal functions via the pituitary have been implicated in cognitive function. Systemically and centrally administered arginine vasopressin (AVP) has been well documented to prolong extinction and improve consolidation in avoidance tasks. However, major questions have centered on the physiological mechanism of action for these effects and whether these cognitive enhancing actions reflect learning or performance. Work with vasopressin antagonists has led to the hypothesis that the effects of systemically administered AVP may be mediated peripherally and may be secondary to increases in blood pressure and activating effects. Centrally administered AVP, however, can also facilitate memory and recent work using an olfactory social memory task suggests that these effects may be mediated, at least in part, by AVP systems in the lateral septum. These results suggest that the cognitive enhancing actions of AVP may involve two parallel, but ultimately homologous, systems at the functional level. Pituitary-derived AVP may facilitate memory actions through more nonspecific (performance) effects, whereas centrally derived AVP may facilitate memory actions through more direct effects on the neural substrates of memory processing in the limbic system.

Animals↗

Solid-state and solution structure of lanthanide complexes of a new nonadentate tripodal ligand containing phenanthroline binding units.

The new nonadentate tripodal ligand trenphen (tris[(1,10-phenanthroline-2-carboxamido)-ethyl]amine) has been synthesized by condensation of tren [tris(2-aminoethyl)amine] with an excess of 1,10-phenanthroline-2-carboxylic acyl chloride. The ligand trenphen and its lanthanide complexes (Sm, Nd, Eu, Tb, and Lu) have been structurally characterized by single-crystal X-ray diffractometry. Crystals of trenphen.H2O.CH3CN, 1, are monoclinic, space group P2(1)/n, a = 14.9923(8) A, b = 17.4451(10) A, c = 17.1880(10) A, beta = 114.8290(10) degrees, V = 4079.9(4) A3, Z = 4. The solid-state crystal structures of the isostructural [Ln(trenphen)](OTf)3.yH2O.xEt2O.zCH3CN (OTf = CF3SO3) (Ln = Nd, y = 0.5, x = 1, z = 3 (2); Ln = Sm, y = 0.5, x = 1, z = 3 (3); Ln = Eu, y = 0.5, z = 3 (4); Ln = Tb, y = 0.5, x = 1, z = 1.5 (5); Ln = Lu, y = 0.5, x = 1, z = 1.5 (6)) (trigonal, P-3, Z = 2) show that the covalent tripod trenphen undergoes a rearrangement in the presence of lanthanide ions yielding three tridentate binding units which encapsulate the nine-coordinated lanthanide ion with a slightly distorted, tricapped, trigonal prismatic coordination geometry. The correlation observed between the decrease of Ln-N distances and the metal ionic radius indicates that trenphen, although containing rigid bidentate phenanthroline units, is sufficiently flexible to self-organize without steric constraints around lanthanide ions of different size. Solution-state NMR studies show that complexes 2-6 exist in acetonitrile solution as discrete rigid C3-symmetric species retaining the triple-helical structure observed in the solid state. NMR and ES-MS titration show the formation of bimetallic and trimetallic species in the presence of an excess of metal, whereas mononuclear bistrenphen complexes are obtained in the presence of an excess of ligand.

Journal Article↗

De novo absence status epilepticus as a benzodiazepine withdrawal syndrome.

A 67-year-old woman with a history of psychotropic drug abuse developed confusion. EEG was consistent with absence status epilepticus (AS). Intravenous (i.v.) flumazenil 1 mg, a benzodiazepine antagonist with anticonvulsant properties, increased both confusion and paroxysmal activity. Complete resolution was obtained after diazepam was administered i.v., and the patient then admitted that she had abruptly discontinued long-standing treatment with carpipramine, amitriptyline, bromazepam, and flunitrazepam. The aggravating effect of flumazenil indicates that benzodiazepine withdrawal was probably the elective triggering factor of this de novo absence status epilepticus.

Aged↗

Angiotensin as neuromodulator/neurotransmitter in central control of body fluid and electrolyte homeostasis.

Stimulation of central angiotensin receptors promotes, among others, drinking behaviour, stimulation of natriuresis and increased release of vasopressin. Angiotensin (ANG II)-containing pathways in the lamina terminalis and the hypothalamic paraventricular (PVN) and supraoptic (SON) nuclei, brain areas involved in the regulation of body fluid homeostasis, have been described. All these areas express predominantly AT1 receptors. The drinking response and the vasopressin release to centrally administered ANG II are mediated by AT1 receptors, while AT2 receptors exert inhibitory effects. Evidence for the involvement of the catecholaminergic and angiotensinergic pathways in the PVN and SON in mediating the ANG II-induced release of vasopressin is presented. ANG II is released in the PVN upon local osmotic stimulation and water deprivation. Finally, we present evidence that activation of central angiotensinergic receptors, water deprivation, or hypertonicity induce transcription of immediate-early genes and expression of the respective proteins in the lamina terminalis and in the PVN and SON. The summarized data implicate ANG II as a neuromodulator/neurotransmitter in central control of body fluid and electrolyte homeostasis.

Angiotensin II↗

[A very high level in a cardiac troponin I assay].

Cardiac troponin I (TnIc) is a very sensitive and also a specific marker of myocardial injuries. We report here, the clinical case of a patient with a particularly important and brutal increase of the troponin during a myocardial infarction. A 64-year-old man was admitted to hospital. He had a myocardial infarction associated to a cardiac necrosis and important cytolysis. The troponin assay was normal when the patient was hospitalized. The angioplasty coronary reperfusion brought about a massive troponin Ic release in systemic circulation: the assay made 10 hours after the appearance of the symptoms shows us an exceptional TnIc concentration that is greater than 4000 microg/L (baseline: 1,5 microg/L). This might be the highest value ever reported.

Humans↗

[Improved reliability of critical data exchange between the biological laboratory and clinical centres. Type of data to transfer and identification of the most relevant tools].

The reliability of the transfer of critical data between the biological laboratory and the clinical centres has to be reassessed. We have a legal constraint (GBEA and best practices) to make sure that the appropriate alert is issued for severe and urgent cases. In this paper, we present a study of the performances of data transfer tools, such as the comparison between regular phone and up to date available means like in line printers and network terminals. This paper focuses on the twenty-four hours duty in the hospital at the same level of reliability for alerts.

Chemistry, Clinical↗