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1.
Nutrients ; 14(21)2022 Oct 28.
Artigo em Inglês | MEDLINE | ID: mdl-36364804

RESUMO

Background: The purpose of this study was to investigate the relationship between folic acid and iron nutrition during pregnancy and congenital heart disease (CHD) in the offspring. Methods: Conditional logistic regression models and nonlinear mixed-effects models were used to analyze the effects of folic acid and iron nutrition during pregnancy on CHD in offspring. Results: After adjusting for confounders, folic acid or iron supplementation during pregnancy reduced the risk for fetal CHD (OR = 0.60 (0.45, 0.82) or 0.36 (0.27, 0.48)). Similarly, dietary iron intake during pregnancy (≥29 mg/d) was associated with a reduced risk of fetal CHD (OR = 0.64 (0.46, 0.88)). Additionally, compared with women who only supplemented folic acid (OR = 0.59 (0.41, 0.84)) or iron (OR = 0.32 (0.16, 0.60)), women who supplemented both folic acid and iron had lower risk for newborns with CHD (OR = 0.22 (0.15, 0.34)). Similarly, compared with women who only supplemented folic acid (OR = 0.59 (0.41, 0.84)) or higher dietary iron intake (≥29 mg/d) (OR = 0.60 (0.33, 1.09)), women who supplemented both folic acid and higher dietary iron intake (≥29 mg/d) had lower risk for the newborn with CHD (OR = 0.41 (0.28, 0.62)). The combined effects were significant in the multiplication model (OR = 0.35 (0.26, 0.48) or 0.66 (0.50, 0.85)) but not in the additive model. Conclusions: Our study found that folic acid and iron nutrition during pregnancy were associated with a reduced risk of CHD in the offspring and confirmed a statistically significant multiplicative interaction between folic acid and iron nutrition on the reduced risk of CHD in offspring.


Assuntos
Ácido Fólico , Cardiopatias Congênitas , Gravidez , Recém-Nascido , Feminino , Humanos , Ferro da Dieta , Estudos de Casos e Controles , Ferro , Fenômenos Fisiológicos da Nutrição Pré-Natal , Suplementos Nutricionais , Cardiopatias Congênitas/epidemiologia , Cardiopatias Congênitas/prevenção & controle
2.
J Org Chem ; 86(23): 17173-17183, 2021 12 03.
Artigo em Inglês | MEDLINE | ID: mdl-34743511

RESUMO

A visible light-promoted radical relay of N-allylbromodifluoroacetamide with quinoxalin-2(1H)-ones was developed in which 5-exo-trig cyclization and C-C bond formation were involved. This protocol was performed under mild conditions to facilely offer a variety of hybrid molecules bearing both quinoxalin-2(1H)-one and 3,3-difluoro-γ-lactam motifs. These prepared novel skeletons would expand the accessible chemical space for structurally complex heterocycles with potential biological activities.


Assuntos
Luz , Quinoxalinas , Ciclização , Lactamas , Estrutura Molecular
3.
Chem Commun (Camb) ; 57(71): 8969-8972, 2021 Sep 06.
Artigo em Inglês | MEDLINE | ID: mdl-34486594

RESUMO

An unprecedented electrochemical heterodifunctionalization of α-CF3 alkenes with benzenesulfonyl hydrazides was accomplished in this work, wherein a ß-sulfonyl and a α-hydroxyl group were simultaneously incorporated across the olefinic double bond in a single operation. Consequently, a series of potentially medicinally valuable and densely functionalized α-trifluoromethyl-ß-sulfonyl tertiary alcohols were assembled under mild conditions. Electrochemically-driven oxidative 1,2-difunctionlization of electron-deficient alkenes well obviates the need for oxidizing reagents, thus rendering this protocol more eco-friendly.

4.
Artigo em Chinês | MEDLINE | ID: mdl-26541040

RESUMO

One hundred and fifty-nine serum samples from hydatid disease patients and 80 serum samples from patients with other liver diseases were detected by gold-immunochromatographic assay, and read by naked eyes and the gold-immunochromatographic test strip reader. The sensitivity, specificity, and accuracy of eye-based method was 92.4% (147/159), 85.0% (68/80), and 89.9% (215/239), which was lower than that of the reader detection (95.6%, 93.7%, 95.0%, respectively). While, its false negative rate (7.5%, 12/159) and false positive rate (15.0%, 12/80) was higher than that of the reader detection (4.4% and 6.3%, respectively).


Assuntos
Cromatografia de Afinidade , Equinococose , Anticorpos Anti-Helmínticos , Ouro , Humanos , Testes Imunológicos , Fitas Reagentes
5.
Zhonghua Liu Xing Bing Xue Za Zhi ; 34(12): 1176-8, 2013 Dec.
Artigo em Chinês | MEDLINE | ID: mdl-24518014

RESUMO

OBJECTIVE: To investigate the prevalence of human and ovine hepatic hydatid disease in Hobukesar Mongolian Autonomous County of Xinjiang (HMACX)and to evaluate the related strategies for prevention and control of the disease. METHODS: A prevalence screening method was used to screen local residents and sheep for hydatid disease in HMACX. Based on B ultrasound images, the screening programs on people and sheep in different sites were carried and the findings were comparatively analyzed. RESULTS: Findings of B ultrasound images through screening program among human beings showed that the positive rates of hydatid diseases 4.4% (23/521), of cystic echinococcosis and alveolar echinococcosis as 4.0% (21/521) and 0.8% (4/521)respectively. The infection rate on sheep was 3.8% (7/180). The positive rates of human and ovine hepatic hydatid disease in Township Chagangule were higher than in other areas. There was no significant statistical difference noticed on human positive rates between Township Chagangule and other areas. Statistically, significant difference for positive rate in ovine was seen between Township Chagangule and Township Bayinaowa(χ(2) = 4.8259, P = 0.0280). As intermediate host of hydatid disease, the infection rate in sheep was higher than that in human beings at Township Chagangule. CONCLUSION: HMACX remained a highly endemic area for human and ovine hydatid disease.


Assuntos
Equinococose Hepática/epidemiologia , Equinococose Hepática/veterinária , Doenças dos Ovinos/parasitologia , Adolescente , Adulto , Idoso , Animais , Criança , Pré-Escolar , China/epidemiologia , Equinococose , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Prevalência , Ovinos , Doenças dos Ovinos/epidemiologia
6.
Zhonghua Gan Zang Bing Za Zhi ; 20(3): 231-5, 2012 Mar.
Artigo em Chinês | MEDLINE | ID: mdl-22475146

RESUMO

OBJECTIVE: To investigate the effects of the histone deacetylase inhibitor, MS-275, on the immune molecule content and categories in hepatocarcinoma exosomes. METHODS: Exosomes were isolated from the human hepatocarcinoma cell lines, HepG2 and Hep3b, and purified by a combination technique of ultrafiltration centrifugation and sucrose gradient ultracentrifugation. The expressions of heat shock protein (HSP)70, human leukocyte antigen (HLA)-I, HLA-DR, cluster of differentiation (CD) 80 and NY-ESO-1 on exosomes were analyzed with immunoelectron microscopy and Western blotting before and after MS-275 treatment. Intergroup differences were statistically analyzed by the Student's paired t-test. RESULTS: MS-275 treatment of both HepG2 and Hep3b cell types significantly increased the numbers of exosomes, their total protein content, and expression of HSP70, HLA-I and CD80 (per 100 exosomes), as compared to non-treated cells (all, P less than 0.01). MS-275 was also found to induce de novo expression of HLA-DR, but had no significant effect on NY-ESO-1 expression (P more than 0.05). The findings from immunoelectron microscopy confirmed those from Western blotting. CONCLUSION: The histone deacetylase inhibitor, MS-275, can significantly alter the immune molecule content and categories in exosomes of hepatocarcinoma cells. The differential expression profile may reflect an anti-cancer immune response and represent molecular targets for novel anti-hepatoma therapeutic or preventative strategies.


Assuntos
Benzamidas/farmacologia , Carcinoma Hepatocelular/metabolismo , Exossomos/metabolismo , Inibidores de Histona Desacetilases/farmacologia , Piridinas/farmacologia , Antígenos de Neoplasias/imunologia , Antígenos de Neoplasias/metabolismo , Carcinoma Hepatocelular/imunologia , Exossomos/imunologia , Células Hep G2 , Antígenos de Histocompatibilidade Classe I/imunologia , Antígenos de Histocompatibilidade Classe I/metabolismo , Humanos
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