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1.
Braz. j. med. biol. res ; 52(6): e7628, 2019. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1001534

RESUMO

This study aimed to explore the influence of gut microbiota alterations induced by Linderae radix ethanol extract (LREE) on alcoholic liver disease (ALD) in rats and to study the anti-inflammatory effect of LREE on ALD through the lipopolysaccharide (LPS) toll-like receptor 4 (TLR4)-nuclear factor kappa B (NF-κB) pathway. ALD rat models were established by intragastric liquor [50% (v/v) ethanol] administration at 10 mL/kg body weight for 20 days. Rats were divided into six groups: normal group (no treatment), model group (ALD rats), Essentiale group (ALD rats fed with Essentiale, 137 mg/kg), and LREE high/moderate/low dose groups (ALD rats fed with 4, 2, or 1 g LREE/kg). NF-κB and LPS levels were evaluated. Liver pathological changes and intestinal ultrastructure were examined by hematoxylin and eosin staining and transmission electron microscopy. The gut microbiota composition was evaluated by 16S rDNA sequencing. Expression levels of TLR4 and CD68 in liver tissue, and occludin and claudin-1 in intestinal tissue were measured. LREE treatment significantly reduced NF-κB and LPS levels, improved liver pathological changes, and ameliorated intestinal ultrastructure injury. Meanwhile, LREE-fed groups showed a higher abundance of Firmicutes and a lower abundance of Bacteroidetes than the rats in the model group. Administration of LREE suppressed TLR4 overexpression and promoted the expression of occludin and claudin-1 in intestine tissue. Thus, LREE could partly ameliorate microflora dysbiosis, suppress the inflammatory response, and attenuate liver injury in ALD rats. The protective effect of LREE might be related to the LPS-TLR4-NF-κB pathway.


Assuntos
Animais , Masculino , Ratos , Extratos Vegetais/farmacologia , Lindera/química , Microbioma Gastrointestinal/efeitos dos fármacos , Inflamação/prevenção & controle , Fígado/ultraestrutura , Hepatopatias Alcoólicas/prevenção & controle , Lipopolissacarídeos/sangue , Citocinas/sangue , Ratos Sprague-Dawley , Proteínas Serina-Treonina Quinases/sangue , Raízes de Plantas/química , Modelos Animais de Doenças , Receptor 4 Toll-Like/sangue , Hepatopatias Alcoólicas/diagnóstico por imagem
2.
Braz. j. med. biol. res ; 52(7): e7374, 2019. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1011596

RESUMO

This study aimed to investigate the association of serum high-mobility group box-1 (HMGB1) and toll-like receptor 4 (TLR4) expressions with the risk of epilepsy as well as their correlations with disease severity and resistance to anti-epilepsy drugs. One hundred and five epilepsy patients and 100 healthy controls (HCs) were enrolled in this case-control study, and serum samples were collected from all participants to assess the HMGB1 and TLR4 expressions by enzyme-linked immunosorbent assay (ELISA). Both serum HMGB1 (P<0.001) and TLR4 (P<0.001) expressions were higher in epilepsy patients than in HCs, and they displayed good predictive values for risk of epilepsy. Moreover, HMGB1 was positively correlated with TLR4 level (r=0.735, P<0.001). HMGB1 and TLR4 levels were both elevated in patients with an average seizure duration >5 min compared to patients with a seizure duration ≤5 min (P=0.001 and P=0.014, respectively). Also, HMGB1 and TLR4 were increased in patients with seizure frequency >3 times per month compared to patients with seizure frequency ≤3 times per month (both P=0.001). In addition, HMGB1 and TLR4 expressions were higher in intractable cases compared to drug-responsive cases (P<0.001). In conclusion, both HMGB1 and TLR4 expressions were correlated with increased risk and severity of epilepsy and their level was higher in patients resistant to anti-epilepsy drugs.


Assuntos
Humanos , Masculino , Feminino , Adulto , Proteína HMGB1/sangue , Epilepsia/sangue , Receptor 4 Toll-Like/sangue , Anticonvulsivantes/uso terapêutico , Índice de Gravidade de Doença , Ensaio de Imunoadsorção Enzimática , Estudos de Casos e Controles , Valor Preditivo dos Testes , Fatores de Risco , Epilepsia/tratamento farmacológico
3.
Braz. j. med. biol. res ; 51(7): e7172, 2018. graf
Artigo em Inglês | LILACS | ID: biblio-889118

RESUMO

The present study was designed to investigate the protective effects and mechanism of inactivated lactobacillus (ILA) on cerebral ischemia reperfusion injury (CIRI) in rats. In this experiment, 30 male Sprague Dawley rats were randomly divided into control group, IRI groups, and ILA group. A middle cerebral artery occlusion and reperfusion model was prepared. The rats were killed after 24 hours of recovery of blood flow of cerebral ischemia resulting from 60-min occlusion. The cerebral infarction volume and neurological scores were assayed by staining and behavioral observation. Malondialdehyde (MDA) and superoxide dismutase (SOD) levels were assayed by biochemical kits. Cell apoptosis was assayed by Tunnel and the Toll-like receptor (TLR)-4, IkB, and A20 were assayed by western blot. The neurobehavioral scores in IRI rats were significantly lower compared to the control group while ILA improved the neurobehavioral scores of the ILA groups. The cerebral infarction volume and neural cell apoptosis of rats in the ILA groups decreased significantly compared with those in the IRI group. In addition, MDA level in the ILA groups decreased whereas SOD activity increased compared to the IRI group. Moreover, ILA also inhibited the expression of TLR-4 and promoted the expression of IkB and A20. ILA inhibited the apoptosis of neural cells, decreased cerebral infarction volume, and reduced oxidative stress through inhibition of TLR-4/NF-kappa B signaling, improving neurobehavioral scores. Thus from the present study it was concluded that ILA has protective effect on CIRI.


Assuntos
Animais , Masculino , Apoptose , Isquemia Encefálica/prevenção & controle , Infarto da Artéria Cerebral Média/complicações , Lacticaseibacillus paracasei , Fármacos Neuroprotetores/administração & dosagem , Traumatismo por Reperfusão/prevenção & controle , Isquemia Encefálica/etiologia , Modelos Animais de Doenças , Regulação para Baixo , NF-kappa B/sangue , Distribuição Aleatória , Ratos Sprague-Dawley , Traumatismo por Reperfusão/etiologia , Receptor 4 Toll-Like/sangue
4.
Braz. j. infect. dis ; 21(5): 545-549, Sept.-Oct. 2017. graf
Artigo em Inglês | LILACS | ID: biblio-1039201

RESUMO

Abstract The present study was aimed to identify the underlying mechanisms of improper renal function in Leishmania donovani infection that causes VL. Mice (BALB/c) were infected with L. donovani and different parameters for proteinuria were assessed. The levels of superoxide anion (O2 -), hydrogen peroxide (H2O2), lipid peroxidation (MDA), inflammatory cytokines, and toll-like receptor (TLR) 2 and 4 expression were found significantly elevated at 60th day in these animals and declined at 90th day post infection. However, TGF-β and caspase 3 activities were higher at 90th day in comparison to 60th day post infection. These findings suggested that exacerbated inflammatory conditions correlate with abnormal renal functions in L. donovani infection, which is further augmented by activated TLRs expressions by circulating leishmanial antigens. Further, the increased levels of TGF-β and caspase 3 at 90th day suggested TGF-β mediated apoptotic cell death of renal and other cells during later stages of disease that may eventually result in release of host and parasitic factors in urine during visceral leishmaniasis.


Assuntos
Animais , Feminino , Ratos , Fator de Crescimento Transformador beta/sangue , Receptor 2 Toll-Like/sangue , Receptor 4 Toll-Like/sangue , Rim/parasitologia , Rim/patologia , Leishmaniose Visceral/patologia , Leishmania donovani , Apoptose , Modelos Animais de Doenças , Leishmaniose Visceral/sangue , Camundongos Endogâmicos BALB C
5.
Journal of Korean Medical Science ; : 979-982, 2006.
Artigo em Inglês | WPRIM | ID: wpr-134503

RESUMO

Toll-like receptors (TLRs) are pattern-recognition receptors that are important in innate immune responses to bacterial infection. The purpose of this study is to describe the prevalence of TLRs genetic variations in the bacteremic patients in Korea. A total of 154 patients with bacteremia and 179 healthy volunteers were included. The Asp299Gly and Thr399Ile allele of the TLR4 gene and Arg753Gln and Arg677Trp allele of the TLR2 gene were tested by PCR-RFLP. The DNA sequences were determined to confirm the PCR-RFLP results. Contrary to the expectation, no genetic polymorphisms were detected in both groups of this study, suggesting that it is very rare in Korean.


Assuntos
Pessoa de Meia-Idade , Masculino , Humanos , Feminino , Receptor 4 Toll-Like/sangue , Receptor 2 Toll-Like/sangue , Fatores de Risco , Medição de Risco/métodos , Prevalência , Polimorfismo de Nucleotídeo Único/genética , Coreia (Geográfico)/epidemiologia , Testes Genéticos/métodos , Predisposição Genética para Doença/epidemiologia , Análise Mutacional de DNA , Biomarcadores/sangue , Bacteriemia/sangue
6.
Journal of Korean Medical Science ; : 979-982, 2006.
Artigo em Inglês | WPRIM | ID: wpr-134502

RESUMO

Toll-like receptors (TLRs) are pattern-recognition receptors that are important in innate immune responses to bacterial infection. The purpose of this study is to describe the prevalence of TLRs genetic variations in the bacteremic patients in Korea. A total of 154 patients with bacteremia and 179 healthy volunteers were included. The Asp299Gly and Thr399Ile allele of the TLR4 gene and Arg753Gln and Arg677Trp allele of the TLR2 gene were tested by PCR-RFLP. The DNA sequences were determined to confirm the PCR-RFLP results. Contrary to the expectation, no genetic polymorphisms were detected in both groups of this study, suggesting that it is very rare in Korean.


Assuntos
Pessoa de Meia-Idade , Masculino , Humanos , Feminino , Receptor 4 Toll-Like/sangue , Receptor 2 Toll-Like/sangue , Fatores de Risco , Medição de Risco/métodos , Prevalência , Polimorfismo de Nucleotídeo Único/genética , Coreia (Geográfico)/epidemiologia , Testes Genéticos/métodos , Predisposição Genética para Doença/epidemiologia , Análise Mutacional de DNA , Biomarcadores/sangue , Bacteriemia/sangue
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