98 research outputs found

    Adriamycin-induced Fetal Hydronephrosis

    Get PDF
    Introduction: At the end of pregnancy, the amniotic fluid (AF) depends basically on renal function, corresponding to fetal urine. Changes in AF, especially oligohydramnios, are reported in association with fetal hydronephrosis (FH). The experimental model using adriamycin in pregnant female rats has a teratogenic effect and has been classically employed to study esophageal atresia. Nevertheless, adriamycin promotes FH with high frequency as well. In the present study, using this animal model, we tried to identify the incidence and microscopic changes of FH, as well as its correlation with AF weight. Materials and Methods: Eight Spreague-Dawley pregnant female rats received adriamycin 2.2 mg/kg on the 8th and 9th gestational days (considering term gestation = 22 days). Those fetuses that received adriamycin (Adriamycin Group) were compared with fetuses from 2 female rats (Control Group), which received 0.9% saline solution. On the 21.5 gestational day, the fetuses were collected by cesarean incision, sacrificed, and examined for macro and microscopic changes in kidneys and ureters. Fetuses with bilateral hydronephrosis formed the Hydronephrosis Group. AF weight was determined as well. Results: Hydronephrosis occurred in 70 (95%) of the 74 fetuses in the adriamycin group against none of the 21 fetuses from the control group. The amniotic fluid weight was increased in the adriamycin group in relation to the control group (p < 0.001). The histomorphometric study revealed dilation of the renal pelvis and reduction of renal parenchyma in the hydronephrosis group in relation to the control group. Severe cortical atrophy, cortical tubular atrophy and medullar atrophy were observed in the hydronephrosis group. Conclusions: Slight renal lesions were in agreement with changes in AF weight, since they suggest that there was production of urine with the maintenance of AF.306508513Brace, R.A., Physiology of amniotic fluid volume regulation (1997) Clin. Obstet. Gynecol., 40, pp. 280-289Harrison, M.R., Nakayama, D.K., Noall, R., de Lorimier, A.A., Correction of congenital hydronephrosis in utero II. Decompression reverses the effects of obstruction on the fetal lung and urinary tract (1982) J. Pediatr. Surg., 17, pp. 965-974Chevalier, R.L., Thornhill, B.A., Chang, A.Y., Unilateral ureteral obstruction in neonatal rats leads to renal insufficiency in adulthood (2000) Kidney Int., 58, pp. 1987-1995Seseke, F., Thelen, P., Hemmerlein, B., Kliese, D., Zoller, G., Ringert, R.H., Histologic and molecular evidence of obstructive uropathy in rats with hereditary congenital hydronephrosis (2000) Urol. Res., 28, pp. 104-109Freedman, A.L., Bukowski, T.P., Smith, C.A., Evans, M.I., Johnson, M.P., Gonzalez, R., Fetal therapy for obstructive uropathy: Diagnosis specific outcomes (1996) J. Urol., 156 (2 PART 2), pp. 720-723. , [corrected]. discussion 723-4Erratum in: J Urol. 1996156: 1786Bernstein, J., Risdon, R.A., Gilbert-Barness, E., Renal System (1997) Potter's, Pathology of the Fetus and Infant, pp. 863-903. , Gilbert-Barness E (ed.), St Louis, MosbyBastide, A., Manning, F., Harman, C., Lange, I., Morrison, I., Ultrasound evaluation of amniotic fluid: Outcome of pregnancies with severe oligohydramnios (1986) Am. J. Obstet. Gynecol., 154, pp. 895-900Reddy, P.P., Mandell, J., Prenatal diagnosis. Therapeutic implications (1998) Urol. Clin. North Amer., 25, pp. 171-180Beasley, S.W., Diez Pardo, J., Qi, B.Q., Tovar, J.A., Xia, H.M., The contribution of the adriamycin-induced rat model of the VATER association to our understanding of congenital abnormalities and their embryogenesis (2000) Pediatr. Surg. Int., 16, pp. 465-472Merei, J., Hasthorpe, S., Farmer, P., Hutson, J.M., Visceral anomalies in prenatally adriamycin-exposed rat fetuses: A model for the VATER association (1999) Pediatr. Surg. Int., 15, pp. 11-16Merei, J., Batiha, A., Hani, I.B., El-Qudah, M., Renal anomalies in the VATER animal model (2001) J. Pediatr. Surg., 36, pp. 1693-1697Franca, W.M., Goncalves, A., Moraes, S.G., Pereira, L.A., Sbragia, L., Esophageal atresia and other visceral anomalies in a modified Adriamycin rat model and their correlations with amniotic fluid volume variations (2004) Pediatr. Surg. Int., 20, pp. 602-608Steinhardt, G.F., Liapis, H., Phillips, B., Vogler, G., Nag, M., Yoon, K.W., Insulin-like growth factor improves renal architecture of fetal kidneys with complete ureteral obstruction (1995) J. Urol., 154, pp. 690-693Steinhardt, G.F., Salinas-Madrigal, L., deMello, D., Farber, R., Phillips, B., Vogler, G., Experimental ureteral obstruction in the fetal Opossum: Histologic assessment (1994) J. Urol., 152, pp. 2133-2138Tewey, K.M., Rowe, T.C., Yang, L., Halligan, B.D., Liu, L.F., Adriamycin-induced DNA damage mediated by mammalian DNA topoisomerase II (1984) Science, 226 (4673), pp. 466-468Orford, J.E., Cass, D.T., Dose response relationship between adriamycin and birth defects in a rat model of VATER association (1999) J. Pediatr. Surg., 34, pp. 392-398Beasley, S.W., Diez Pardo, J., Qi, B.Q., Tovar, J.A., Xia, H.M., The contribution of the adriamycin-induced rat model of the VATER association to our understanding of congenital abnormalities and their embryogenesis (2000) Pediatr. Surg. Int., 16, pp. 465-472Kimble, R.M., Harding, J.E., Kolbe, A., Does gut atresia cause polyhydramnios? (1998) Pediatr. Surg. Int., 13, pp. 115-117Liu, M.I., Hutson, J.M., Cloacal and urogenital malformations in adriamycin-exposed rat fetuses (2000) BJU Int., 86, pp. 107-112Liu, M.I., Hutson, J.M., Zhou, B., Critical timing of bladder embryogenesis in an adriamycin-exposed rat fetal model: A clue to the origin of the bladder (1999) J. Pediatr. Surg., 34, pp. 1647-165

    Genomic analysis of two phlebotomine sand fly vectors of Leishmania from the New and Old World.

    Get PDF
    Phlebotomine sand flies are of global significance as important vectors of human disease, transmitting bacterial, viral, and protozoan pathogens, including the kinetoplastid parasites of the genus Leishmania, the causative agents of devastating diseases collectively termed leishmaniasis. More than 40 pathogenic Leishmania species are transmitted to humans by approximately 35 sand fly species in 98 countries with hundreds of millions of people at risk around the world. No approved efficacious vaccine exists for leishmaniasis and available therapeutic drugs are either toxic and/or expensive, or the parasites are becoming resistant to the more recently developed drugs. Therefore, sand fly and/or reservoir control are currently the most effective strategies to break transmission. To better understand the biology of sand flies, including the mechanisms involved in their vectorial capacity, insecticide resistance, and population structures we sequenced the genomes of two geographically widespread and important sand fly vector species: Phlebotomus papatasi, a vector of Leishmania parasites that cause cutaneous leishmaniasis, (distributed in Europe, the Middle East and North Africa) and Lutzomyia longipalpis, a vector of Leishmania parasites that cause visceral leishmaniasis (distributed across Central and South America). We categorized and curated genes involved in processes important to their roles as disease vectors, including chemosensation, blood feeding, circadian rhythm, immunity, and detoxification, as well as mobile genetic elements. We also defined gene orthology and observed micro-synteny among the genomes. Finally, we present the genetic diversity and population structure of these species in their respective geographical areas. These genomes will be a foundation on which to base future efforts to prevent vector-borne transmission of Leishmania parasites

    Aspectos microscópicos da interação feijoeiro-Colletotrichum lindemuthianum mediados pelo silício

    Get PDF
    A antracnose, causada pelo fungo Colletotrichum lindemuthianum, é uma das doenças mais destrutivas que afetam a cultura do feijoeiro. Com o objetivo de encontrar alternativas para o controle dessa doença, o presente trabalho investigou, em nível microscópico, o efeito do silício (Si) na resistência do feijoeiro à infecção por C. lindemuthianum. Plantas de feijoeiro (cv. Pérola) foram cultivadas em solução nutritiva contendo 0 (-Si) ou 2 mM (+Si) de Si e inoculadas no estádio de crescimento V4 com uma suspensão de conídios de C. lindemuthianum. A severidade da antracnose decresceu cerca de 52% nas folhas das plantas supridas com Si (4,4%) em relação às folhas das plantas não supridas (8,5%). Observações de folhas de feijoeiro das plantas não supridas com Si no microscópio eletrônico de varredura revelaram alterações morfológicas nas nervuras em contraste com as folhas de plantas supridas com Si. Utilizando-se a microanálise de raios-X, verificou-se maior concentração dos minerais enxofre, potássio e Si nas folhas das plantas supridas com Si. Em conclusão, o suprimento de Si em plantas de feijoeiro foi importante para reduzir os sintomas da antracnose
    corecore