4 research outputs found

    Atividade sexual e doenças sexualmente transmissíveis em escolares do 2º grau de Rio Branco-Acre, Brasil La actividad sexual y las enfermedades sexualmente trasmisibles en estudiantes de segundo grado (estudios secundarios) de Rio Branco-Acre, Brasil Sexual activity and sexually transmissible diseases of high school students in Rio Branco-Acre, Brasil

    Get PDF
    Este estudo foi realizado junto a 2.684 alunos do Segundo Grau de Rio Branco¾Acre, Brasil, para verificar aspectos da atividade sexual e a ocorrência de DST/AIDS. Dos alunos pesquisados, 48,9% tiveram relações sexuais, sendo que para o sexo masculino o início mais freqüente foi aos 13 anos, representando 34,3% e para o feminino foi aos 16 anos, com 31,6%. Da ocorrência de DST/AIDS mencionadas 58,4% foi para a Hepatite B, 39,4% para a Monilíase e 2,2% para a Gonorréia. Dos que tiveram relações sexuais 47,6% foi com o/a namorado/a, 25,8% com o/a vizinho/a e 10,5% com a empregada doméstica. Como conclusão, 52,3% dos alunos das escolas particulares, 50,0% da federal, 45,7% das estaduais e 41,8% da municipal, tiveram relação sexual.<br>Este estudio se realizó con 2.684 estudiantes de secundaria de Rio Branco-Acre, Brasil, para verificar los aspectos de la actividad sexual y la incidencia de ETS/SIDA. De los estudiantes investigados 48,9% tuvieron relaciones sexuales. De ellos el 34,3% pertenecen al sexo masculino y empezaron a los 13 años de edad. 31,6% son del sexo femenino e iniciaron su vida sexual a los 16 años. De la incidencia referida de ETS/SIDA el 58,4% fue para Hepatitis B, el 39,4% para Candidiasis y el 2,2% para Gonorrea. De los que tuvieron relaciones sexuales, el 47,6% fue con el novio (¾a); el 25,8% con el vecino (-a) y el 10,5% con la empleada domestica de la casa. Por lo tanto, se concluye que el 52,3% de los alunnos de las escuelas privadas, el 50,0% de la federal, el 45,7% de las estatales y el 41,8% de las municipales (provinciales) tuvieron relación sexual.<br>This study was realized with 2.684 students of the high school in Rio Branco¾Acre, Brazil, to verify aspects of the sexual activity and the occurrence of DST/AIDS. From the researched students, 48,9% had sexual intercourses, and the largest frequency was 34,3% for male sex, with the beginning at 13 years old, and for female sex 31,6%, with the beginning at 16 years old. The occurrence of mentioned DST/AIDS was: 58,4% for Hepatite B, 39,4% for Monilíase and 2,2% for Gonorrhea. Among those ones who had their first sexual intercourse, 47,6% were with the boyfriend, 25,8% with the neighbor and 10,5% with the domestic maid. Concluding, the students who had sexual intercourses were 52,3% of private schools, 50,0% of federal ones, 45,7% of state ones and 41,8% of municipal ones

    3-[4′-bromo-(1,1′-biphenyl)-4-y1]-n,n-dimethyl-3- (2-thienyl)-2-propen-1-amine: Synthesis, Cytotoxicity, And Leishmanicidal, Trypanocidal And Antimycobacterial Activities

    No full text
    Current therapies for Chagas' disease, leishmaniasis and tuberculosis are unsatisfactory because of the failure rates, significant toxicity and/or drug resistance. In this study, the compound 3-[4′-bromo- (1,1′-biphenyl)- 4-yl] -N,N-dimethyl-3- (2-thienyl) -2-propen-1-amine (IV) was synthesized and its trypanocidal, leishmanicidal and antimycobacterial activities were investigated. The cytotoxicity was determined on V79 cells with three endpoints: nucleic acid content, 3-(4,5-dimethylthiazole- 2-yl)-2,5-diphenyl tetrazolium bromide reduction and Neutral Red uptake. This compound was active against different species of mycobacteria and different life cycle stages of Trypanosoma cruzi. In experiments with trypomastigotes performed at 4° C in the presence of blood, the activity was 8.8-fold more active than the standard drug, Crystal Violet. Higher activity was achieved against Leishmania amazonensis, with an ED50/24 h of 3.0 ± 0.3 μmol/L. The effect against trypanosomatids, which suggests high activity of compound IV against promastigotes of L. amazonensis and amastigotes of T. cruzi, stimulated further studies in vitro with amastigotes interiorized in macrophages and with in vivo models. Our results indicate that mammalian V79 cells are less susceptible to the action of compound IV than promastigotes of L. amazonensis (8.0-13.3-fold) and axenic amastigotes of T. cruzi (3.5-5.9-fold).505629637Bleed, D., Watt, C., Dye, C., (2000) Global Tuberculosis. Control, 275, pp. 1-175. , WHO/CDS/TB/2000 Geneva, SwitzerlandGbayisomore, A., Lardizabal, A.A., Reichman, L.B., Update: Prevention and treatment of tuberculosis (2000) Current Opinion in Infectious Disease, 13, pp. 155-159(1998) Weekly Epidemiology Records, 1-2, p. 1. , World Health Organization. Chagas diseaseAlbrecht, H., Sobottka, I., Emminger, C., Jablonowski, H., Just, G., Stoehr, A., Visceral leishmaniasis emerging as an important opportunistic infection in HIV-infected persons living in areas nonendemic for Leishmania donovani (1996) Archives of Pathology and Laboratory Medicine, 120, pp. 189-198Badri, M., Ehrlich, R., Wood, R., Pulerwitz, T., Maartens, G., Association between tuberculosis and HIV disease progression in a high tuberculosis prevalence area (2001) International Journal of Tuberculosis and Lung Disease, 5, pp. 225-232Espinal, M.A., Laszlo, A., Simonsen, L., Boulahbal, F., Kim, S.J., Reniero, A., Global trends in resistance to antituberculosis drugs (2001) New England Journal of Medicine, 344, pp. 1294-1303Thomas, S.M., McPhee, D.G., Crystal violet: A direct-acting frameshift mutagen whose mutagenicity is enhanced by mammalian metabolism (1984) Mutation Research, 140, pp. 165-167De Castro, S.L., The challenge of Chagas' disease chemotherapy: An update of drugs assayed against Trypanosoma cruzi (1993) Acta Tropica, 53, pp. 83-98Urbina, J.A., Chemotherapy of Chagas' disease: The how and the why (1999) Journal of Molecular Medicine, 77, pp. 332-338Croft, S.L., Pharmacological approaches to antitrypanosomal chemotherapy (1997) Memórias Do Instituto Oswaldo Cruz, 94, pp. 215-220Leon, L.L., Machado, G.M.C., Barral, A., Carvalho-Paes, L.E., Grimaldi G., Jr., Antigenic differences among Leishmania amazonensis isolates and their relationship with the clinical forms of the disease (1992) Memórias Do Instituto Oswaldo Cruz, 87, pp. 229-234Olliaro, P.L., Bryceson, A.D.M., Practical progress and new drugs for changing patterns of leishmaniasis (1993) Parasitology Today, 9, pp. 323-328Pereira, D.G., De Castro, S.L., Durán, N., Activity of N,N-dimethyl-1-2- propen-1-amine derivatives in mice experimentally infected with Trypanosoma cruzi (1998) Acta Tropica, 69, pp. 205-211De Souza, A.O., Santos Júnior, R.R., Ferreira-Júlio, J.F., Rodriguez, J.A., Melo, P.S., Haun, M., Synthesis, antimycobacterial activities and cytotoxicity on V79 of 3-(4′-bromo1,1m-biphenyl-4-yl)-3- (4-x-phenyl)- N,N-dimethyl- 2-propen-1-amine derivatives (2001) European Journal of Medicinal Chemistry, 36, pp. 843-850De Souza, A.O., Durán, N., Synthesis and antileishmaniasis activities of N,N-dimethyl- 2-propen-1-amine derivatives (1998), Brazilian Patent PIBr. 9902748-8De Souza, A.O., Sato, D.N., Aily, D.C.G., Durán, N., In vitro activity of N,N-dimethyl- 2-propen-1-amines against Mycobacterium tuberculosis (1998) Journal of Antimicrobial Chemotherapy, 42, pp. 407-408De Conti, R., Gimenez, S.M.N., Haun, M., Pilli, R.A., De Castro, S.L., Durán, N., Synthesis and biological activities of N,N-dimethyl-2- propen-1-amine derivatives (1996) European Journal of Medicinal Chemistry, 31, pp. 1-4Cingi, M.R., De Angelis, I., Fortunati, E., Reggiani, D., Bianchi, V., Tiozzo, R., Choice and standardization of test protocols in cytotoxicology: A multicentre approach (1991) Toxicology In Vitro, 5, pp. 119-125Denizot, F., Lang, R., Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability (1986) Journal of Immunological Methods, 89, pp. 271-277Borenfreund, E., Puerner, J.A., A simple quantitative procedure using monolayer cultures for cytotoxicity assays (HTD/VN 90) (1984) Journal of Tissue Culture Methods, 9, pp. 7-9Collins, L.A., Franzblau, S.G., Microplate Alamar Blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium (1997) Antimicrobial Agents and Chemotherapy, 41, pp. 1004-1009Silva, L.H.P., Nussenszweig, V., Sobre uma cepa de Trypanosoma cruzi virulenta para o camundongo branco (1953) Folia Clinica Biologica, 20, pp. 191-207De Castro, S.L., Meirelles, M.N.L., Oliveira, M.M., Trypanosoma cruzi: Adrenergic modulation of cAMP role in proliferation and differentiation of amastigotes in vitro (1987) Experimental Parasitology, 64, pp. 368-375De Castro, S.L., Pinto, M.C.F.R., Pinto, A.V., Screening of natural and synthetic drugs against Trypanosoma cruzi. 1-Establishing a structure/activity relationship (1994) Microbios, 78, pp. 83-90De Castro, S.L., Soeiro, M.N.C., Higashi, K.O., Meirelles, M.N.L., Differential effect of amphotericin B on the three evolutive stages of Trypanosoma cruzi and on the host cell-parasite interaction (1993) Brazilian Journal of Medical and Biological Research, 26, pp. 1219-1229Grimaldi G., Jr., David, J.R., McMahon-Pratt, D., Identification and distribution of New World Leishmania species characterized by serodeme analysis using monoclonal antibodies (1987) American Journal of Tropical Medicine and Hygiene, 36, pp. 270-287De Reuck, A.V.S., Cameron, M.P., The reversible activation of lysosomes in normal cells and the effect of pathological conditions (1963) Lysosomes, pp. 362-375. , (De Reuck, A. V. S. & Cameron, M. P., Eds) Little, Brown & Co., Boston, MA, USASchlemper, B.R., Chiari, E., Brener, Z., Growth inhibition drug test with Trypanosoma cruzi culture forms (1977) Journal of Protozoology, 24, pp. 544-547De Castro, S.L., Soeiro, M.N.C., Meirelles, M.N.L., Trypanosoma cruzi: Effect of phenothiazines on the parasite and on its interaction with host cells (1992) Memórias Do Instituto Oswaldo Cruz, 87, pp. 209-215Lopes, J.N., Cruz, F.S., Do Campo, R., Vasconcellos, M.E., Sampaio, M.C.R., Pinto, A.V., In vitro and in vivo evaluation of the toxicity of 1,4-naphthoquinone and 1,2-naphthoquinone derivatives against Trypanosoma cruzi (1978) Annals of Tropical Medicine and Parasitology, 72, pp. 523-531Rovai, L.E., Aoki, A., Gerez de Burgos, N.M., Blanco, A., Effect of gossypol on trypomastigotes and amastigotes of Trypanosoma cruzi (1990) Journal of Protozoology, 37, pp. 280-286Neves-Pinto, C., Dantas, A.P., De Moura, K.C.G., Emery, F.S., Polequevitch, P.F., Pinto, M.C.F.R., Chemical reactivity studies with naphthoquinones from Tabebuia with antitrypanosomal efficacy (2000) Arzneimittel- Forschung-Drug Research, 50, pp. 1120-1128Araujo, C.A.C., Alegrio, L.V., Leon, L.L., Antileishmanial activity of compounds extracted and characterized from Centrolobium sclerophyllum (1998) Phytochemistry, 49, pp. 751-754Marsden, P.D., Sampaio, R.N.R., Carvalho, E.M., Veiga, J.P.T., Costa, J.L.M., Llanoscuentas, E.A., High continuous antimony therapy in two patients with unresponsive mucosal leishmaniasis (1985) American Journal of Tropical Medicine and Hygiene, 34, pp. 710-713Afrin, F., Dey, T., Anam, K., Ali, N., Leishmanicidal activity of stearylamine-bearing liposomes in vitro (2001) Journal of Parasitology, 87, pp. 188-193Wiese, M., Gorckel, I., Homologues of LMPK, a mitogen-activated protein kinase from Leishmania mexicana, in different Leishmania species (2001) Medical Microbiology and Immunology, 190, pp. 19-22Croft, S.L., Yardley, V., Chemotherapy of leishmaniasis (2002) Current Pharmaceutical Design, 8, pp. 319-342Loiseau, P.M., Bories, C., Recent strategies for the chemotherapy of visceral leishmaniasis (1999) Current Opinion in Infectious Diseases, 12, pp. 559-564Escobar, P., Matu, S., Croft, S.L., Sensitivities of Leishmania species to hexadecylphosphocholine (miltefosine), ET-18-OCH3 (edelfosine) and amphotericin B (2002) Acta Tropica, 81, pp. 151-157Escobar, P., Yardley, V., Croft, S.L., Activities of hexadecylphosphocholine (miltefosine), AmBisome, and sodium stibogluconate (Pentostam) against Lerishmania donovani in immunodeficient scid mice (2001) Antimicrobial Agents and Chemotherapy, 45, pp. 1872-1875Kayser, O., Kiderlen, A.F., Laatsch, H., Croft, S.L., In vitro leishmanicidal activity of monomeric and dimeric naphthoquinones (2000) Acta Tropica, 77, pp. 307-314Valderrama, J., Fournet, A., Valderrama, C., Bastias, S., Astudillo, C., De Arias, A., Synthesis and in vitro antiprotozoal activity of thiophene ring-containing quinones (1999) Chemical and Pharmaceutical Bulletin, 47, pp. 1221-1226Ram, V.J., Goel, A., Shukla, P.K., Kapil, A., Synthesis of thiophenes and thieno[3,2-c]pyran-4-ones as antileishmanial and antifungal agents (1997) Bioorganic and Medicinal Chemistry Letters, 7, pp. 3101-3106Nussbaumer, P., Ryder, N.S., Stutz, A., Allylamine antimycotics-recent trends in structure- activity-relationships and syntheses (1991) Pesticide Science, 31, pp. 437-455Nussbaumer, P., Petranyi, G., Stutz, A., Synthesis and structure-activity- relationships of benzo[b]thienylallylamine antimycotics (1991) Journal of Medicinal Chemistry, 34, pp. 65-73Stutz, A., Georgopoulos, A., Granitzer, W., Petranyi, G., Berney, D., Synthesis and structure-activity relationships of naftifine-related allylamine antimycotics (1986) Journal of Medicinal Chemistry, 29, pp. 112-12
    corecore