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1.
Virol J ; 12: 10, 2015 Feb 03.
Artigo em Inglês | MEDLINE | ID: mdl-25645259

RESUMO

BACKGROUND: After the 1968 H3N2 pandemic emerged in humans, H3N2 influenza viruses continuously circulated and evolved in nature. An H3N2 variant was circulating in humans in the 1990s and subsequently introduced into the pig population in the 2000s. This virus gradually became the main subtype of swine influenza virus worldwide. However, there were no reports of infections in dogs with this virus. FINDINGS: In 2013, 35 nasal swabs from pet dogs were positive for Influenza A virus by RT-PCR. Two viruses were isolated and genetically characterized. In the phylogenetic trees of all gene segments, two H3N2 canine isolates clustered with Moscow/10/99 and most H3N2 swine influenza viruses. These results indicated that two H3N2 CIVs possessed high homology with human/swine influenza viruses, which at the same time exhibited some amino acid substitutions in NA, polymerase basic protein 1 (PB1), and nucleoprotein (NP), which probably were related to the interspecies transmission. CONCLUSIONS: These two viruses share the highest homology with swine H3N2, Moscow/99-like viruses, which indicated that these viruses might originate from swine viruses.


Assuntos
Doenças do Cão/virologia , Vírus da Influenza A Subtipo H3N2/classificação , Vírus da Influenza A Subtipo H3N2/isolamento & purificação , Infecções por Orthomyxoviridae/veterinária , Animais , China , Análise por Conglomerados , Cães , Vírus da Influenza A Subtipo H3N2/genética , Dados de Sequência Molecular , Mutação de Sentido Incorreto , Mucosa Nasal/virologia , Infecções por Orthomyxoviridae/virologia , Animais de Estimação , Filogenia , RNA Viral/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Análise de Sequência de DNA , Homologia de Sequência , Proteínas Virais/genética
2.
Zhonghua Nan Ke Xue ; 18(5): 472-4, 2012 May.
Artigo em Zh | MEDLINE | ID: mdl-22741449

RESUMO

OBJECTIVE: To evaluate the effects of tadalafil administered on demand or once a day in the treatment of erectile dysfunction (ED). METHODS: We randomly assigned 61 ED patients to three groups to receive tadalafil on demand, at 5 mg once daily, and at 10 mg once daily, respectively. After 42 days of medication, we compared the therapeutic effects among different groups using the patients' sexual encounter profile (SEP) diaries, detected the adverse reactions and assessed the safety of tadalafil. RESULTS: Fifty-three (86.7%) of the patients completed the investigation, and all responded well to tadalafil medication, with a significantly improved success rate of sexual intercourse and a low rate of mild adverse effects. The mean positive rates of SEP were basically similar between the on-demand and once-daily groups. CONCLUSION: There are no significant differences in the improvement of penile erection and sexual satisfaction of ED patients treated by on-demand and once-daily administration of tadalafil.


Assuntos
Carbolinas/administração & dosagem , Disfunção Erétil/tratamento farmacológico , Inibidores de Fosfodiesterase/administração & dosagem , Adulto , Carbolinas/efeitos adversos , Carbolinas/uso terapêutico , Esquema de Medicação , Humanos , Masculino , Inibidores de Fosfodiesterase/efeitos adversos , Inibidores de Fosfodiesterase/uso terapêutico , Tadalafila , Resultado do Tratamento
3.
Kaohsiung J Med Sci ; 37(7): 583-593, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-33611824

RESUMO

The present study aimed to investigate the role of apigenin and the molecular mechanism of miR-152-5p and bromodomain containing 4 (BRD4) in the proliferation, invasion, and epithelial-mesenchymal transition (EMT) of cervical carcinoma cells. Quantitative real-time PCR was used to detect the transfection efficiency and the expression of miR-152-5p and BRD4. Western blotting was conducted to evaluate the protein level of BRD4, E-cadherin, N-cadherin, and MMP9. Luciferase reporter assay was performed to confirm whether miR-152-5p bound to BRD4. MTT and Transwell invasion assay were applied to determine the cell proliferation and invasion, respectively. MiR-152-5p was downregulated and BRD4 was upregulated in cervical carcinoma tissue. Besides, miR-152-5p could directly bind to BRD4 in Hela and CaSki cells. In addition, apigenin inhibited proliferation, invasion, and EMT of Hela and CaSki cells by regulating miR-152-5p/BRD4 axis. Apigenin suppresses proliferation, invasion, and induced EMT of cervical carcinoma cells by regulation of miR-152-5p/BRD4 axis.


Assuntos
Apigenina/farmacologia , Carcinoma/tratamento farmacológico , Proteínas de Ciclo Celular/biossíntese , Proliferação de Células/efeitos dos fármacos , Transição Epitelial-Mesenquimal/efeitos dos fármacos , Regulação Neoplásica da Expressão Gênica , MicroRNAs/biossíntese , Fatores de Transcrição/biossíntese , Neoplasias do Colo do Útero/tratamento farmacológico , Linhagem Celular Tumoral , Movimento Celular , Feminino , Células HeLa , Humanos , Invasividade Neoplásica , Proteínas Nucleares/metabolismo , Sais de Tetrazólio/química , Tiazóis/química , Fatores de Transcrição/metabolismo
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