Browsing
     by title


0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

or enter first few letters:   
OK
Full Text
Peer Reviewed
See detail16-kDa prolactin and bromocriptine in postpartum cardiomyopathy.
Hilfiker-Kleiner, Denise; Struman, Ingrid ULg; Hoch, Melanie et al

in Current Heart Failure Reports (2012), 9(3), 174-82

Peripartum cardiomyopathy (PPCM) is a potentially life-threatening heart disease emerging toward the end of pregnancy or in the first postpartal months in previously healthy women. Recent data suggest a ... [more ▼]

Peripartum cardiomyopathy (PPCM) is a potentially life-threatening heart disease emerging toward the end of pregnancy or in the first postpartal months in previously healthy women. Recent data suggest a central role of unbalanced peri-/postpartum oxidative stress that triggers the proteolytic cleavage of the nursing hormone prolactin (PRL) into a potent antiangiogenic, proapoptotic, and proinflammatory 16-kDa PRL fragment. This notion is supported by the observation that inhibition of PRL secretion by bromocriptine, a dopamine D2-receptor agonist, prevented the onset of disease in an animal model of PPCM and by first clinical experiences where bromocriptine seem to exert positive effects with respect to prevention or treatment of PPCM patients. Here, we highlight the current state of knowledge on diagnosis of PPCM, provide insights into the biology and pathophysiology of 16-kDa PRL and bromocriptine, and outline potential consequences for the clinical management and treatment options for PPCM patients. [less ▲]

Detailed reference viewed: 37 (2 ULg)
Full Text
Peer Reviewed
See detailThe 16-kilodalton N-terminal fragment of human prolactin is a potent inhibitor of angiogenesis
Clapp, Carmen; Martial, Joseph ULg; Guzman, Raphaël C et al

in Endocrinology (1993), 133(3), 1292-9

The formation of a new blood supply, angiogenesis, is an essential component of carcinogenesis and unrestricted tumor growth. A substance capable of inhibiting angiogenesis would be of considerable ... [more ▼]

The formation of a new blood supply, angiogenesis, is an essential component of carcinogenesis and unrestricted tumor growth. A substance capable of inhibiting angiogenesis would be of considerable therapeutic potential in the treatment of cancer. We previously reported that the 16-kilodalton N-terminal fragment of rat PRL (16K rPRL) was a potent inhibitor of capillary endothelial cell proliferation via a novel receptor. We now report that the nanomolar concentrations of recombinant human 16K PRL inhibit basal and basic fibroblast growth factor- or vascular endothelial growth factor-stimulated growth of bovine brain capillary endothelial cells. 16K human (h) PRL also inhibits stimulation of human umbilical vein endothelial cell proliferation by basic fibroblast growth factor. The organization of endothelial cells into capillary-like structures in type I collagen gels is also prevented by 16K hPRL. Furthermore, in an in vivo assay, the chick embryo chorioallantoic membrane assay, 16K hPRL as well as 16K rPRL were potent inhibitors of capillary formation. 16K hPRL, like 16K rPRL, maintains its biological activity as a partial PRL agonist at PRL receptors on mammary gland epithelial cells. These data demonstrate for the first time that the biological activity of 16K rPRL is not unique and that similar fragments of hPRL are active. The antiangiogenic activity of these molecules is conserved across avian and mammalian species. That 16K hPRL is a potent antiangiogenic factor in in vitro and an in vivo assay raises the exciting potential of this peptide being capable of inhibiting tumor growth. [less ▲]

Detailed reference viewed: 36 (4 ULg)
Peer Reviewed
See detail16. En dessous de 0,5 g/l dans le sang, est-il vrai que l'alcool n'augmente pas le risque d'accident ?
Charlier, Corinne ULg; DEVILLE, Marine ULg; DENOOZ, Raphael ULg

in Seutin, Vincent; Scuvée-Moreau, Jacqueline; Quertemont, Etienne (Eds.) L'alcool en questions (2015)

L’alcool remonte le moral. Une petite cuite n’a jamais tué personne. Boire un café atténue l’effet de l’alcool. Le binge drinking est un fléau nouveau… De nombreuses idées reçues, certaines fondées ... [more ▼]

L’alcool remonte le moral. Une petite cuite n’a jamais tué personne. Boire un café atténue l’effet de l’alcool. Le binge drinking est un fléau nouveau… De nombreuses idées reçues, certaines fondées, d’autres pas, sont véhiculées à propos de l’alcool et de ses conséquences. L’alcool soulève aussi de multiples questions : L’alcool est-il une drogue ? L’alcool est-il aphrodisiaque ? L’alcoolisme est-il héréditaire ? Combien l’alcool coûte/rapporte-t-il à la société ? Peut-on guérir de l’alcoolisme ?… Ce livre a pour but de démont(r)er certaines idées reçues sur l’alcool et d’apporter des réponses aux questions que chacun se pose. Les auteurs ne se bornent pas à répondre par vrai ou faux, ils fournissent les explications, appuyées sur l’état des connaissances scientifiques actuelles, qui permettent d’infirmer ou de confirmer ces idées reçues ou de répondre à ces questions. Ils nuancent le propos lorsque la réponse n’est pas de l’ordre du tout ou rien. Il est indéniable que l’excès d’alcool est nuisible à la santé. Il existe cependant une littérature scientifique démontrant des effets positifs sur la santé de la consommation en quantités modérées de certaines boissons alcoolisées. Ce mélange d’effets positifs et négatifs explique que le public a développé une relation d’amour-haine avec l’alcool. Ainsi, les abstinents complets sont parfois qualifiés de rabat-joie. Les alcooliques chroniques (5 à 10 % des occidentaux, selon les études épidémiologiques !) sont, quant à eux, souvent trop vite jugés. Ce qui est certain c’est que l’alcoolo-dépendance est source de beaucoup de souffrances pour la personne et son entourage. Ces 41 réponses à des questions sur l’alcool visent à donner des balises au lecteur, littérature scientifique à l’appui. [less ▲]

Detailed reference viewed: 8 (0 ULg)
See detail1609, la révolution de l'observation
Nazé, Yaël ULg

Article for general public (2009)

Not Available

Detailed reference viewed: 31 (4 ULg)
Peer Reviewed
See detail16K hPRL prevents angiogenesis by inducing both apoptosis and cell cycle arrest of endothelial cells
Tabruyn, Sébastien ULg; Sorlet, Catherine; Georges, Angélique et al

Poster (2003)

Detailed reference viewed: 10 (1 ULg)
Full Text
Peer Reviewed
See detail16K Human Prolactin Inhibits Vascular Endothelial Growth Factor-Induced Activation of Ras in Capillary Endothelial Cells
D'Angelo, Gisela; Martini, Jean-François; Iiri, Taroh et al

in Molecular Endocrinology (Baltimore, Md.) (1999), 13(2), 692-704

Signaling pathways mediating the antiangiogenic action of 16K human (h)PRL include inhibition of vascular endothelial growth factor (VEGF)-induced activation of the mitogen-activated protein kinases (MAPK ... [more ▼]

Signaling pathways mediating the antiangiogenic action of 16K human (h)PRL include inhibition of vascular endothelial growth factor (VEGF)-induced activation of the mitogen-activated protein kinases (MAPK). To determine at which step 16K hPRL acts to inhibit VEGF-induced MAPK activation, we assessed more proximal events in the signaling cascade. 16K hPRL treatment blocked VEGF-induced Raf-1 activation as well as its translocation to the plasma membrane. 16K hPRL indirectly increased cAMP levels; however, the blockade of Raf-1 activation was not dependent on the stimulation of cAMP-dependent protein kinase (PKA), but rather on the inhibition of the GTP-bound Ras. The VEGF-induced tyrosine phosphorylation of the VEGF receptor, Flk-1, and its association with the Shc/Grb2/Ras-GAP (guanosine triphosphatase-activating protein) complex were unaffected by 16K hPRL treatment. In contrast, 16K hPRL prevented the VEGF-induced phosphorylation and dissociation of Sos from Grb2 at 5 min, consistent with inhibition by 16K hPRL of the MEK/MAPK feedback on Sos. The inhibition of Ras activation was paralleled by the increased phosphorylation of 120 kDa proteins comigrating with Ras-GAP. Taken together, these findings show that 16K hPRL inhibits the VEGF-induced Ras activation; this antagonism represents a novel and potentially important mechanism for the control of angiogenesis. [less ▲]

Detailed reference viewed: 32 (3 ULg)
Peer Reviewed
See detail16K human prolactin is an anti-lymphangiogenic factor in vitro and in vivo
Kinet, Virginie; Castermans, Karolien; Blacher, Silvia ULg et al

Poster (2010, March)

Detailed reference viewed: 12 (0 ULg)
Peer Reviewed
See detail16K human prolactin is an anti-lymphangiogenic factor in vitro and in vivo
Kinet, Virginie; Castermans, Karolien; Blacher, Silvia ULg et al

Poster (2010, May 21)

Detailed reference viewed: 13 (2 ULg)
Full Text
Peer Reviewed
See detailThe 16OH/18OH and OD/OH isotope ratios in comet C/2002 T7 (LINEAR)
Hutsemekers, Damien ULg; Manfroid, Jean ULg; Jehin, Emmanuel ULg et al

in Astronomy and Astrophysics (2008), 490(Letters), 31-34

The [SUP]16[/SUP]OH/[SUP]18[/SUP]OH and OD/OH isotope ratios are measured in the Oort-Cloud comet C/2002 T7 (LINEAR) through ground-based observations of the OH A [SUP]2[/SUP]Σ[SUP]+[/SUP] - X [SUP]2 ... [more ▼]

The [SUP]16[/SUP]OH/[SUP]18[/SUP]OH and OD/OH isotope ratios are measured in the Oort-Cloud comet C/2002 T7 (LINEAR) through ground-based observations of the OH A [SUP]2[/SUP]Σ[SUP]+[/SUP] - X [SUP]2[/SUP]Π[SUB]i[/SUB] ultraviolet bands at 3063 à (0, 0) and 3121 à (1, 1) obtained with the Very Large Telescope (VLT) feeding the Ultraviolet-Visual Echelle Spectrograph (UVES). From the [SUP]16[/SUP]OH/[SUP]18[/SUP]OH ratio, we find [SUP]16[/SUP]O/[SUP]18[/SUP]O = 425 ± 55, equal within the uncertainties to the terrestrial value and to the ratio measured in other comets, although marginally smaller. We also estimate OD/OH from which we derive D/H = 2.5 ± 0.7à 10[SUP]-4[/SUP] in water. This value is compatible with the water D/H ratios evaluated in other comets and is marginally higher than the terrestrial value. Based on observations collected at the European Southern Observatory, Paranal, Chile (ESO Programme 073.C-0525). [less ▲]

Detailed reference viewed: 11 (1 ULg)
Full Text
Peer Reviewed
See detailA 17,900-year multi-proxy lacustrine record of Lago Puyehue (Chilean Lake District): introduction
De Batist, Marc; Fagel, Nathalie ULg; Loutre, Marie-France et al

in Journal of Paleolimnology (2008), 39(2), 151-161

This paper introduces the background and main results of a research project aimed at unravelling the paleolimnological and paleoclimatological history of Lago Puyehue (40 degrees S, Lake District, Chile ... [more ▼]

This paper introduces the background and main results of a research project aimed at unravelling the paleolimnological and paleoclimatological history of Lago Puyehue (40 degrees S, Lake District, Chile) since the Last Glacial Maximum (LGM), based on the study of several sediment cores from the lake and on extensive fieldwork in the lake catchment. The longest record was obtained in an 11-m-long piston core. An age-depth model was established by AMS C-14 dating, Pb-210 and Cs-237 measurements, identification of event-deposits, and varve-counting for the past 600 years. The core extends back to 17,915 cal. yr. BP, and the seismic data indicate that an open-lake sedimentary environment already existed several thousands of years before that. The core was submitted to a multi-proxy analysis, including sedimentology, mineralogy, grain-size, major geochemistry and organic geochemistry (C/N ratio, delta C-13), loss-on-ignition, magnetic susceptibility, diatom analysis and palynology. Along-core variations in sediment composition reveal that the area of Lago Puyehue was characterized since the LGM by a series of rapid climate fluctuations superimposed on a long-term warming trend. Identified climate fluctuations confirm a.o. the existence of a Late-Glacial cold reversal predating the northern-hemisphere Younger Dryas cold period by 500-1,000 years, as well as the existence of an early southern-hemisphere Holocene climatic optimum. Varve-thickness analyses over the past 600 years reveal periodicities similar to those associated with the El Nino Southern Oscillation and the Pacific Decadal Oscillation, as well as intervals with increased precipitation, related to an intensification of the El Nino impact during the southern-hemisphere equivalent of the Little Ice Age. [less ▲]

Detailed reference viewed: 605 (6 ULg)
Full Text
Peer Reviewed
See detailLe 17-butyrate d'hydrocortisone (Locoid), un trentenaire toujours innovateur.
Pierard, Gérald ULg

in Revue Médicale de Liège (2006), 61(2), 128-30

Since half a century, dermocorticoids represent worthy compounds in dermatological therapy. About thirty years ago, hydrocortisone 17-butyrate was introduced on the Belgian market. This compound combines ... [more ▼]

Since half a century, dermocorticoids represent worthy compounds in dermatological therapy. About thirty years ago, hydrocortisone 17-butyrate was introduced on the Belgian market. This compound combines good efficiency and reduced risk of side effects. Its topical formulations have been enriched over time. The original Locoid lipocream and Locoid Crelo presentations confer remarkable qualities to the product. We report a synopsis of clinical and translational studies devoted to this unique dermocorticoid. [less ▲]

Detailed reference viewed: 202 (2 ULg)
Full Text
See detail17-O-acetyl, 10-hydroxycorynantheol, a selective antiplasmodial alkaloid isolated from Strychnos usambarensis leaves
Cao, Martine ULg; Muganga, Raymond ULg; Tits, Monique ULg et al

Conference (2011, May 13)

In the course of our investigations on Strychnos usambarensis leaves in order to isolate isostrychnopentamine, the main alkaloid responsible for the antiplasmodial activity of the plant, a new tertiary ... [more ▼]

In the course of our investigations on Strychnos usambarensis leaves in order to isolate isostrychnopentamine, the main alkaloid responsible for the antiplasmodial activity of the plant, a new tertiary indolic alkaloid has been isolated: 17-O-acetyl, 10-hydroxycorynantheol 1. Its structure was determined by means of spectroscopic and spectrometric methods such as UV, IR, CD, NMR and ESI-MS. 17-O-acetyl, 10-hydroxycorynantheol 1 is one of the most active monomeric indole alkaloid known to date showing an in vitro activity against Plasmodium falciparum close to 5 µM and a high selectivity. [less ▲]

Detailed reference viewed: 40 (10 ULg)
Full Text
Peer Reviewed
See detail17-O-Acetyl,10-hydroxycorynantheol, a Selective Antiplasmodial Alkaloid Isolated from Strychnos usambarensis Leaves
Cao, Martine ULg; Muganga, Raymond ULg; Tits, Monique ULg et al

in Planta Medica (2011), 77

In the course of our investigations on Strychnos usambarensis leaves in order to isolate isostrychnopentamine, the main alkaloid responsible for the antiplasmodial activity of the plant, a new tertiary ... [more ▼]

In the course of our investigations on Strychnos usambarensis leaves in order to isolate isostrychnopentamine, the main alkaloid responsible for the antiplasmodial activity of the plant, a new tertiary indolic alkaloid has been isolated: 17-O-acetyl, 10-hydroxycorynantheol 1. Its structure was determined by means of spectroscopic and spectrometric methods such as UV, IR, CD, NMR and ESI-MS. 17-O-acetyl, 10-hydroxycorynantheol 1 is one of the most active monomeric indole alkaloid known to date showing an in vitro activity against Plasmodium falciparum close to 5 µM and a high selectivity. [less ▲]

Detailed reference viewed: 70 (21 ULg)
See detail17-O-Actetyl-10-hydroxycorynantheol, a selective antiplasmodial alkaloid isolated from Strychnos usambarensis leaves
Cao, Martine ULg; Muganga, Raymond ULg; Tits, Monique ULg et al

Conference (2011, December 13)

In the course of our investigations on Strychnos usambarensis leaves in order to isolate isostrychnopentamine, the main alkaloid responsible for the antiplasmodial activity of the plant, a new tertiary ... [more ▼]

In the course of our investigations on Strychnos usambarensis leaves in order to isolate isostrychnopentamine, the main alkaloid responsible for the antiplasmodial activity of the plant, a new tertiary indolic alkaloid has been isolated: 17-O-acetyl, 10-hydroxycorynantheol 1. Its structure was determined by means of spectroscopic and spectrometric methods such as UV, IR, CD, NMR and ESI-MS. 17-O-acetyl, 10-hydroxycorynantheol 1 is one of the most active monomeric indole alkaloid known to date showing an in vitro activity against Plasmodium falciparum close to 5 µM and a high selectivity. [less ▲]

Detailed reference viewed: 26 (7 ULg)
See detail1798: contre les républicains français, une identité belge a posteriori
Raxhon, Philippe ULg; van Ypersele, Laurence

in Bruneel, Claude; Bernard, Bruno (Eds.) Les prémices de l'identité belge avant 1830? (2006)

Detailed reference viewed: 29 (3 ULg)