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13篇 您的检索式:作者名="Matheus N"
    题名 作者 年代 出处 被引量
1Melatonin inhibits serotonin transporter activity in intestinal epithelial cells显示文摘Matheus N Mendoza C Iceta R 2010J Pineal Res2010,48,4:1
2Melatonin inhibits serotonin transporter activity in intestinal epithelial cells显示文摘Matheus N Mendoza C Iceta R 2010J Pineal Res2010,48,4:1
3Humanization of nursing care: what is it? 显示文摘Corbani N M Brfitas A C Matheus M C 2009Rev Bras Enferm2009,62,3:1
4Novel transcrip- tional targets of the SRY-HMG box transcription factor SOX4 link its expression to the development of small cell lung cancer显示文摘Castillo SD Matheu A Mariani N 2012Cancer Res2012,72,1:1
5Humanization of nursing care: what is it? 显示文摘Corbani N M Br(e)tas A C Matheus M C 2009Rev Bras Enferm2009,62,3:1
6Emergence of NDM-1-producing Klebsiella pneumoniae in Guatemala显示文摘Fernando Pasteran Ezequiel Albornoz Diego Faccone Sonia Gomez Claudia Valenzuela Melissa Morales Pavela Estrada Laura Valenzuela Jorge Matheu Leonor Guerriero Enrique Arbizú Yeraldine Calderón Pilar Ramon-Pardo Alejandra Corso 2012Journal of Antimicrobial Chemotherapy2012,,7:1
7IL-10 modulates serotonin transporter activity and molecular expression in intestinal epithelial cells显示文摘Latorre E Mendoza C Matheus N 2013Cytokine2013,61,3:1
8Fresh embryo transfer versus frozen embryo transfer in in vitro fertilization cycles: a systematic review and meta-analysis显示文摘Matheus Roque Karinna Lattes Sandra Serra Ivan Solà Selmo Geber Ramón Carreras Miguel Angel Checa 2012Fertility and Sterility2012,,:1
9Lipopolysaccharide induces alteration of serotonin transporter in human intestinal epithelial cells显示文摘Mendoza C Matheus N Iceta R 2009Innate Immun2009,15,4:1
10Melatonin inhibits serotonin transporter activity in intestinal epithelial cells 显示文摘Matheus N Mendoza C Iceta R 2010J Pineal Res2010,48,4:1
11Novel transcriptional tar- gets of the SRY-HMG box transcription factor SOX4 link its expres- sion to the development of small cell lung cancer显示文摘Castillo SD Matheu A Mariani N 2012Cancer Res2012,72,1:1
12aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilidederivatives 显示文摘CLEITON A N MATHEUS P F 2013J Microbiol Methods2013,94,3:1
13Rifaximin on epigenetics and autophagy in animal model of hepatocellular carcinoma secondary to metabolic-dysfunction associated steatotic liver disease显示文摘BACKGROUND Prevalence of hepatocellular carcinoma(HCC)is increasing,especially in patients with metabolic dysfunctionassociated steatotic liver disease(MASLD).AIM To investigate rifaximin(RIF)effects on epigenetic/autophagy markers in animals.METHODS Adult Sprague-Dawley rats were randomly assigned(n=8,each)and treated from 5-16 wk:Control[standard diet,water plus gavage with vehicle(Veh)],HCC[high-fat choline deficient diet(HFCD),diethylnitrosamine(DEN)in drinking water and Veh gavage],and RIF[HFCD,DEN and RIF(50 mg/kg/d)gavage].Gene expression of epigenetic/autophagy markers and circulating miRNAs were obtained.RESULTS All HCC and RIF animals developed metabolic-dysfunction associated steatohepatitis fibrosis,and cirrhosis,but three RIF-group did not develop HCC.Comparing animals who developed HCC with those who did not,miR-122,miR-34a,tubulin alpha-1c(Tuba-1c),metalloproteinases-2(Mmp2),and metalloproteinases-9(Mmp9)were significantly higher in the HCC-group.The opposite occurred with Becn1,coactivator associated arginine methyltransferase-1(Carm1),enhancer of zeste homolog-2(Ezh2),autophagy-related factor LC3A/B(Map1 Lc3b),and p62/sequestosome-1(p62/SQSTM1)-protein.Comparing with controls,Map1 Lc3b,Becn1 and Ezh2 were lower in HCC and RIF-groups(P<0.05).Carm1 was lower in HCC compared to RIF(P<0.05).Hepatic expression of Mmp9 was higher in HCC in relation to the control;the opposite was observed for p62/Sqstm1(P<0.05).Expression of p62/SQSTM1 protein was lower in the RIF-group compared to the control(P=0.024).There was no difference among groups for Tuba-1c,Aldolase-B,alpha-fetoprotein,and Mmp2(P>0.05).miR-122 was higher in HCC,and miR-34a in RIF compared to controls(P<0.05).miR-26b was lower in HCC compared to RIF,and the inverse was observed for miR-224(P<0.05).There was no difference among groups regarding miR-33a,miR-143,miR-155,miR-375 and miR-21(P>0.05).CONCLUSION RIF might have a possible beneficial effect on preventing/delaying liver carcinogenesis through epigenetic modulation in a rat model of MASLD-HCC.Matheus Truccolo Michalczuk Larisse Longo Melina Belén Keingeski Bruno de Souza Basso Gabriel Tayguara Silveira Guerreiro Jessica T Ferrari JoséEduardo Vargas Cláudia P Oliveira Carolina Uribe-Cruz Carlos Thadeu Schmidt Cerski Eduardo Filippi-Chiela Mário ReisÁlvares-da-Silva 2024World Journal of Hepatology2024,16,1:0
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