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1.
Life (Basel) ; 12(3)2022 Mar 17.
Artigo em Inglês | MEDLINE | ID: mdl-35330193

RESUMO

Db/db mice (carrying a mutation in the gene encoding leptin receptor) show autophagy suppression. Our aim was to evaluate the effect of autophagy inducer trehalose on liver and heart autophagy in db/db mice and to study inflammation dysregulation and the suitability of chitinases' expression levels as diabetes markers. Thirty-eight male db/db mice and C57/BL mice (control) were used. The db/db model manifested inflammation symptoms: overexpression of TNF-α in the spleen and underexpression of IL-10 in the liver and spleen (cytokine imbalance). Simultaneously, we revealed decreased expression of chitotriosidase (CHIT1) and acid mammalian chitinase (CHIA) in the liver of db/db mice. CHIA expression in db/db mice is significantly lower only in the spleen. Trehalose treatment significantly reduced blood glucose concentration and glycated hemoglobin. Treatment of db/db mice by trehalose was followed by increased autophagy induction in the heart and liver (increased autolysosomes volume density studied by morphometric electron-microscopic method). Trehalose exerted beneficial cardiac effects possibly via increased lipophagy (uptake of lipid droplets). The autophagy activation by trehalose had several positive effects on the heart and liver of db/db mice; therefore, lipophagy activation seems to be a promising therapy for diabetes.

2.
Genet Test Mol Biomarkers ; 18(12): 791-6, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25390410

RESUMO

We determined the frequencies of null mutations of the FLG gene--2282del4, R501X, R2447X, 3702delG, S3247X, and the 12-repeat allele (rs12730241)--among 460 Caucasians of the city of Novosibirsk, Russia. The frequency was 17.7% for rs12730241, 2.73% for 2282del4, 0.22% for R501X, 0.33% for R2447X, and 0% for 3702delG and S3247X in a western Siberian population. A case-control study showed that the deletion 2282del4 was associated with atopic dermatitis in children (odds ratio 7.01; p<0.001). The other mutations were not.


Assuntos
Sequência de Bases , Dermatite Atópica/genética , Proteínas de Filamentos Intermediários/genética , Deleção de Sequência , Adolescente , Adulto , Idoso , Estudos de Casos e Controles , Criança , Pré-Escolar , Dermatite Atópica/epidemiologia , Feminino , Proteínas Filagrinas , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Sibéria/epidemiologia
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