Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Biol Pharm Bull ; 44(11): 1746-1751, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34719650

RESUMO

Tramadol is a weak opioid that produces analgesic effect via both the µ-opioid receptor (MOR) and non-opioid targets. Constipation is the most common opioid-related side effect in patients with cancer and non-cancer pain. However, the contribution of MOR to tramadol-induced constipation is unclear. Therefore, we used naldemedine, a peripherally acting MOR antagonist, and MOR-knockout mice to investigate the involvement of peripheral MOR in tramadol-induced constipation using a small intestinal transit model. A single dose of tramadol (3-100 mg/kg, per os (p.o.)) inhibited small intestinal transit dose-dependently in rats. Naldemedine (0.01-10 mg/kg, p.o.) blocked the inhibition of small intestinal transit induced by tramadol (30 mg/kg, p.o.) in rats. The transition rate increased dose-dependently over the range of naldemedine 0.01-0.3 mg/kg, and complete recovery was observed at 0.3-10 m/kg. Additionally, tramadol (30 and 100 mg/kg, subcutaneously (s.c.)) inhibited small intestinal transit in wild-type mice but not in MOR-knockout mice. These results suggest that peripheral MOR participates in tramadol-induced constipation.


Assuntos
Analgésicos Opioides/efeitos adversos , Constipação Induzida por Opioides/etiologia , Receptores Opioides mu/efeitos dos fármacos , Tramadol/efeitos adversos , Analgésicos Opioides/sangue , Analgésicos Opioides/farmacocinética , Animais , Intestino Delgado/efeitos dos fármacos , Masculino , Naltrexona/efeitos adversos , Naltrexona/análogos & derivados , Naltrexona/sangue , Naltrexona/farmacocinética , Nociceptividade/efeitos dos fármacos , Constipação Induzida por Opioides/metabolismo , Ratos , Ratos Sprague-Dawley , Ratos Wistar , Receptores Opioides mu/metabolismo , Tramadol/sangue , Tramadol/farmacocinética
2.
J Vet Med Sci ; 76(11): 1487-91, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25070691

RESUMO

Fecal egg count reduction tests (FECRT) and larval migration inhibition tests (LMIT) were conducted to assess the efficacy of ivermectin (IVM) against gastrointestinal nematodes on 2 cattle farms in northern Japan in 2009 and 2010. Twelve to 20 calves on each farm were treated topically with 0.5 mg IVM/kg 2 (Farm 2) or 4 times (Farm 1) during the grazing season (May-October). On Farm 1, fecal egg count (FEC) reduction at 14 days post-treatment ranged from 16 to 87% in 2009 and from 24 to 96% in 2010, with relatively low reductions in August and October (16-53%). Conversely, IVM treatment on Farm 2 reduced FEC by 97% in September 2009. Larvae obtained from fecal cultures and identified by PCR-RFLP analysis revealed that the dominant species on both farms prior to IVM administration was Cooperia oncophora. In 2009, the FEC reduction of C. oncophora on Farm 1 decreased from 85% in May to 56% in August. In 2010, the reduction in C. oncophora in August was 28%. In the LMIT using larvae collected from the fecal cultures on Farm 1 in May and August 2009, the EC50 value of IVM in C. oncophora in August (0.892 µg/ml) was 3 times higher than that in May (0.296 µg/ml). The results of the LMIT corroborated the FECRT data, indicating the presence of IVM-resistant C. oncophora on Farm 1, at least in August. This is the first report of IVM-resistant nematodes in Japanese cattle.


Assuntos
Doenças dos Bovinos/tratamento farmacológico , Doenças dos Bovinos/parasitologia , Resistência a Medicamentos/genética , Trato Gastrointestinal/parasitologia , Ivermectina/uso terapêutico , Infecções por Nematoides/veterinária , Animais , Bovinos , Fezes/parasitologia , Ivermectina/farmacologia , Japão , Infecções por Nematoides/tratamento farmacológico , Contagem de Ovos de Parasitas/veterinária , Reação em Cadeia da Polimerase/veterinária , Polimorfismo de Fragmento de Restrição , Estações do Ano , Especificidade da Espécie
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA