69 research outputs found
Flutuação de unidades formadoras de colĂŽnias de fungos entomopatogĂȘnicos prĂłximas ao solo.
Variabilidade de resposta de subpopulaçÔes de Euschistus heros (F.) a mistura de tiametoxam e lambda cialotrina.
Biologia e exigĂȘncias tĂ©rmicas do ĂĄcaro vermelho Tetranychus gigas Pritchard e Baker em soja.
bitstream/item/71549/1/ID-30974.pd
DinĂąmica populacional do ĂĄcaro verde Mononychellus planki em cultivares de soja.
bitstream/item/71543/1/ID-30978.pd
Fruit and vegetable intake and risk of cancer in the Swedish womenâs lifestyle and health cohort
Objective To investigate whether intake of fruits and
vegetables is associated with overall cancer incidence in a
large prospective cohort of women in Sweden characterised by young age at enrolment (30â49 years) and relatively low intake of fruits and vegetables.
Methods We followed prospectively 49,261 women, who
completed a food frequency questionnaire in 1991â1992. A
total of 2,347 incident invasive cancer cases were identified
until December 2006. The occurrence of cancer was analysed by fitting Poisson regression models, estimating incidence rate ratios (RR) and 95% confidence intervals (CI).
Results The median intake of fruits and vegetables was
204 g/day (10th; 90th percentile: 37; 564 g/day). Intake of
fruits and vegetables was not statistically significantly associated with overall cancer incidence. When we compared
women in the highest quintile of fruit and vegetable intake to
women in the lowest quintile, the RR for overall cancer was
1.01 (95% CI: 0.88â1.16). Similar results were obtained when
investigating the effect of intake of fruits and vegetables
separately and when we stratified women by age at follow-up.
Conclusion Fruit and vegetable intake was not associated
with risk of total cancer in this prospective cohort of
women in Sweden
Pletismografia respiratória por indutùncia: estudo comparativo entre calibração por manobra de isovolume e calibração qualitativa diagnóstica em voluntårios saudåveis avaliados em diferentes posturas
3,3âČDiindolylmethane Suppresses Vascular Smooth Muscle Cell Phenotypic Modulation and Inhibits Neointima Formation after Carotid Injury
3,3'Diindolylmethane (DIM), a natural phytochemical, has shown inhibitory effects on the growth and migration of a variety of cancer cells; however, whether DIM has similar effects on vascular smooth muscle cells (VSMCs) remains unknown. The purpose of this study was to assess the effects of DIM on the proliferation and migration of cultured VSMCs and neointima formation in a carotid injury model, as well as the related cell signaling mechanisms.DIM dose-dependently inhibited the platelet-derived growth factor (PDGF)-BB-induced proliferation of VSMCs without cell cytotoxicity. This inhibition was caused by a G0/G1 phase cell cycle arrest demonstrated by fluorescence-activated cell-sorting analysis. We also showed that DIM-induced growth inhibition was associated with the inhibition of the expression of cyclin D1 and cyclin-dependent kinase (CDK) 4/6 as well as an increase in p27(Kip1) levels in PDGF-stimulated VSMCs. Moreover, DIM was also found to modulate migration of VSMCs and smooth muscle-specific contractile marker expression. Mechanistically, DIM negatively modulated PDGF-BB-induced phosphorylation of PDGF-recptorÎČ (PDGF-RÎČ) and the activities of downstream signaling molecules including Akt/glycogen synthase kinase(GSK)3ÎČ, extracellular signal-regulated kinase1/2 (ERK1/2), and signal transducers and activators of transcription 3 (STAT3). Our in vivo studies using a mouse carotid arterial injury model revealed that treatment with 150 mg/kg DIM resulted in significant reduction of the neointima/media ratio and proliferating cell nuclear antigen (PCNA)-positive cells, without affecting apoptosis of vascular cells and reendothelialization. Infiltration of inflammatory cells was also inhibited by DIM administration.These results demonstrate that DIM can suppress the phenotypic modulation of VSMCs and neointima hyperplasia after vascular injury. These beneficial effects on VSMCs were at least partly mediated by the inhibition of PDGF-RÎČ and the activities of downstream signaling pathways. The results suggest that DIM has the potential to be a candidate for the prevention of restenosis
Interaction between Red Meat Intake and NAT2 Genotype in Increasing the Risk of Colorectal Cancer in Japanese and African Americans
Heterocyclic aromatic amines formed in cooked meat may be an underlying mechanism for the red meat-colorectal cancer (CRC) association. These compounds require bioactivaction by N-acetyltransferase 2 (NAT2). An interaction effect between red meat consumption and NAT2 in increasing CRC risk has been inconsistently reported in whites. We investigated this interaction in two populations in which the high-activity rapid NAT2 phenotype is 10- and 2-fold more common than in whites. We meta-analyzed four studies of Japanese (2,217 cases, 3,788 controls) and three studies of African Americans (527 cases, 4,527 controls). NAT2 phenotype was inferred from an optimized seven-SNP genotyping panel. Processed and total red meat intakes were associated with an increased CRC risk in Japanese and in both ethnic groups combined (Pâs †0.002). We observed an interaction between processed meat intake and NAT2 in Japanese (P = 0.04), African Americans (P = 0.02), and in both groups combined (P = 0.006). The association of processed meat with CRC was strongest among individuals with the rapid NAT2 phenotype (combined analysis, OR for highest vs. lowest quartile: 1.62, 95% CI: 1.28â2.05; Ptrend = 8.0Ă10â5), intermediate among those with the intermediate NAT2 phenotype (1.29, 95% CI: 1.05â1.59; Ptrend = 0.05) and null among those with the slow phenotype (Ptrend = 0.45). A similar interaction was found for NAT2 and total red meat (Pinteraction = 0.03). Our findings support a role for NAT2 in modifying the association between red meat consumption and CRC in Japanese and African Americans
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