13 research outputs found

    Exposure to Maternal Diabetes Induces Salt-Sensitive Hypertension and Impairs Renal Function in Adult Rat Offspring

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    OBJECTIVE—Epidemiological and experimental studies have led to the hypothesis of fetal origin of adult diseases, suggesting that some adult diseases might be determined before birth by altered fetal development. We have previously demonstrated in the rat that in utero exposure to maternal diabetes impairs renal development leading to a reduction in nephron number. Little is known on the long-term consequences of in utero exposure to maternal diabetes. The aim of the study was to assess, in the rat, long-term effects of in utero exposure to maternal diabetes on blood pressure and renal function in adulthood

    Endocrine Disruption and Organochlorine Pesticides

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    Le plus ancien rĂ©cit de lutte contre la pollution remonte Ă  une lĂ©gende indienne racontant que la divinitĂ© Sing-bonga Ă©tait incommodĂ©e par les Ă©manations des fours dans lesquels les Asuras fondaient leurs mĂ©taux (1). Evidemment depuis, la problĂ©matique n–a cessĂ© de s–accroĂźtre et la contamination de la Terre par de nombreux polluants est devenue aujourd–hui un problĂšme majeur de notre SociĂ©tĂ©. La protection de notre environnement est une question capitale qui doit ĂȘtre respectĂ©e malgrĂ© la pression Ă©conomique actuelle et qui ne cessera de croĂźtre au cours des prochaines annĂ©es mĂȘme si l–identification objective et indiscutable de ce qui est essentiel – donc devant ĂȘtre prioritairement garanti sur la planĂšte – est difficile Ă  cerner (2). « Un oiseau en mauvais Ă©tat ne pond pas de bons oeufs » disait un proverbe grec. Mais ce n–est qu–à partir de la seconde moitiĂ© du XXĂšme siĂšcle que les toxicologues ont commencĂ© Ă  identifier les effets qu–avaient entraĂźnĂ©s Ă  l–échelle mondiale les pollutions Ă©mises aux XIXĂšme siĂšcle sur la faune sauvage et sur le cheptel (3). L–histoire contemporaine des pesticides industriels commence vers 1874 (synthĂšse des organochlorĂ©s) et se poursuit tout au long de ces 2 siĂšcles en passant par la synthĂšse des organophosphorĂ©s (1950), des carbamates (1970) et des pyrĂ©throĂŻdes (1975) (4). Le dichlorodiphĂ©nyltrichloroĂ©thane (DDT) a Ă©tĂ© synthĂ©tisĂ© pour la premiĂšre fois par un Ă©tudiant en cours de prĂ©paration de sa thĂšse de doctorat : Othmer Zeidler. La production, reprise par les entreprises F.Mayo puis par la Geigy Co. a d–abord intĂ©ressĂ© l–armĂ©e, puis l–agriculture. DĂšs la fin de la 2Ăšme guerre mondiale, des mises en garde furent lancĂ©es Ă  propos des effets nocifs du produit (4). Un dĂ©clin des populations de grives, d–aigles chauves, d–orfaies et de mammifĂšres consommateurs de poissons fut constatĂ© Ă  partir des annĂ©es 50 et dĂ©noncĂ© par Rachel Carson dans son cĂ©lĂšbre appel du « Silent Spring » de 1962. Bien qu–il soit interdit en Occident depuis les annĂ©es 70, ce produit a Ă©tĂ© tellement utilisĂ© et prĂ©sente une rĂ©manence si longue qu–une contamination ubiquitaire existe aujourd–hui encore. De plus, ce produit continue Ă  ĂȘtre produit aux USA pour ĂȘtre utilisĂ© Ă  des fins de dĂ©moustification dans les pays en voie de dĂ©veloppement. Il en va de mĂȘme de l–HexachlorobenzĂšne (HCB), un autre organochlorĂ© dont l–usage est interdit sous nos latitudes, mais reste frĂ©quent dans d–autres pays. Ces deux exemples indiquent que le problĂšme de la contamination continue Ă  nous concerner, mĂȘme pour des produits dont l–usage est aujourd–hui strictement rĂ©glementĂ© ou interdit. Des effets sur la faune semblent encore actuellement devoir ĂȘtre attribuĂ©s Ă  ces produits. La diminution de la population des phoques dans la mer de Wadden pourrait ĂȘtre due Ă  la forte contamination en composants organochlorĂ©s des poissons dont ces phoques se nourrissent (5). ExposĂ© au DDT et Ă  son mĂ©tabolite dichlorodiphenyldichloroĂ©thylĂšne (DDE), le Seratherodon mossambicus prĂ©sente une rĂ©duction de la sĂ©crĂ©tion de cortisol par une action toxique cytospĂ©cifique sur l–axe hypothalamo-hypophysaire (6). Des travaux rĂ©cents ont montrĂ© que le DDT et le DDE se lient chez les oiseaux et les mammifĂšres au moyen de liaisons covalentes aux cellules de la zona fasciculata - homologue du tissu interrĂ©nal du poisson - induisant des microhĂ©morragies. Cette « dĂ©faillance » cortisolique peut s–accompagner d–une perturbation du mĂ©tabolisme glucidique et notamment d–un taux Ă©levĂ© de glycogĂšne hĂ©patique (7). Les pesticides organochlorĂ©s (DDT, DDE) entraĂźnent Ă©galement des perturbations d–ordre mĂ©tabolique chez certaines espĂšces d–oiseaux, notamment le faucon pĂšlerin en Grande Bretagne et les oiseaux piscivores des grands lacs nord amĂ©ricains oĂč l–on a constatĂ© au cours des annĂ©es 1960 que leur reproduction Ă©tait menacĂ©e et qu–une des manifestations les plus Ă©videntes des perturbations observĂ©es Ă©tait le taux Ă©levĂ© de malformations (8). Des mortalitĂ©s Ă©levĂ©es de poissons ou de coquillages ont Ă©tĂ© rapportĂ©es dans des Ă©levages situĂ©s Ă  proximitĂ© des zones d–épandage de pesticides organophosphorĂ©s et de carbamates. En 1991, la dispersion aĂ©rienne de fenitrothion dans le but de provoquer la dĂ©moustication en Languedoc a Ă©tĂ© Ă  l–origine de la perte de plusieurs tonnes de crevettes japonaises. L–utilisation de trichlorfon et de dichlorvos comme antiparasitaires dans des fermes d–élevages de saumons a provoquĂ© des Ă©pisodes de mortalitĂ© importante (9).Xenoestrogens such organochlorine pesticides are known to induce changes in reproductive development, function or behaviour in wildlife. Because these compounds are able to modify the estrogens metabolism, or to compete with estradiol for binding to the estrogen receptor, it may be possible that these products affect the risk of developing impaired fertility, precocious puberty or some kinds of cancer in man

    The Use of Cyclosporine A in Rheumatology: a 2016 Comprehensive Review

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    Cyclosporine A, an inhibitor of calcineurin, exerts an immunomodulator action interfering with T cell activation. Even though novel therapeutic tools have emerged, CyA still represents a suitable option in several clinical rheumatology settings. This is the case of refractory nephritis and cytopenias associated with systemic lupus erythematosus. Furthermore, CyA is a valued therapeutic tool in the management of uveitis and thrombophlebitis in course of Behçet's disease. Topical CyA has been proven to be beneficial in the dry eye of Sjogren's syndrome, whereas oral treatment with CyA can be considered for the severe complications of adult onset Still's disease. CyA provides a therapeutic option in psoriatic arthritis, being rather effective in skin disease. CyA is currently regarded as a second-line option for patients with inflammatory myopathies refractory to standard regimen. CyA is used even in paediatric rheumatology, in particular in the management of juvenile dermatomyositis and macrophage activation syndrome associated with systemic juvenile idiopathic arthritis. Importantly, CyA has been shown to suppress the replication of HCV, and it can thus be safely prescribed to those patients with chronic hepatitis C. Noteworthy, CyA can be administered throughout the gestation course. Surely, caution should be paid to CyA safety profile, in particular to its nephrotoxicity. Even though most evidence comes from small and uncontrolled studies with few randomised controlled trials, CyA should be still regarded as a valid therapeutic tool in 2016 rheumatology

    Birth weight, malnutrition and kidney-associated outcomes--a global concern

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    An adverse intrauterine environment is associated with an increased risk of elevated blood pressure and kidney disease in later life. Many studies have focused on low birth weight, prematurity and growth restriction as surrogate markers of an adverse intrauterine environment; however, high birth weight, exposure to maternal diabetes and rapid growth during early childhood are also emerging as developmental risk factors for chronic diseases. Altered programming of nephron number is an important link between exposure to developmental stressors and subsequent risk of hypertension and kidney disease. Maternal, fetal, and childhood nutrition are crucial contributors to these programming effects. Resource-poor countries experience the sequential burdens of fetal and childhood undernutrition and subsequent overnutrition, which synergistically act to augment the effects of developmental programming; this observation might explain in part the disproportionate burden of chronic disease in these regions. Numerous nutritional interventions have been effective in reducing the short-term risk of low birth weight and prematurity. Understanding the potential long-term benefits of such interventions is crucial to inform policy decisions to interrupt the developmental programming cycle and stem the growing epidemics of hypertension and kidney disease worldwide
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