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1.
Commun Biol ; 3(1): 1, 2020 01 07.
Artigo em Inglês | MEDLINE | ID: mdl-31925316

RESUMO

The domestic Bactrian camels were treated as one of the principal means of locomotion between the eastern and western cultures in history. However, whether they originated from East Asia or Central Asia remains elusive. To address this question, we perform whole-genome sequencing of 128 camels across Asia. The extant wild and domestic Bactrian camels show remarkable genetic divergence, as they were split from dromedaries. The wild Bactrian camels also contribute little to the ancestry of domestic ones, although they share close habitat in East Asia. Interestingly, among the domestic Bactrian camels, those from Iran exhibit the largest genetic distance and the earliest split from all others in the phylogeny, despite evident admixture between domestic Bactrian camels and dromedaries living in Central Asia. Taken together, our study support the Central Asian origin of domestic Bactrian camels, which were then immigrated eastward to Mongolia where native wild Bactrian camels inhabit.


Assuntos
Camelus/classificação , Camelus/genética , Genoma , Genômica , Migração Animal , Animais , Ásia , Evolução Molecular , Variação Genética , Genética Populacional , Genômica/métodos , Filogenia , Polimorfismo de Nucleotídeo Único , Sequenciamento Completo do Genoma
2.
Acta Pharm ; 66(4): 555-562, 2016 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-27749254

RESUMO

The aim of this study was to prepare a nasal gel of risperidone and to investigate the pharmacokinetics and relative bioavailability of the drug in rats. Compared with oral dosing, the risperidone nasal gel exhibited very fast absorption and high bioavailability. Maximal plasma concentration (cmax) and the time to reach cmax (tmax) were 15.2 µg mL-1 and 5 min for the nasal gel, 3.6 µg mL-1 and 30 min for the oral drug suspension, respectively. Pharmacokinetic parameters such as tmax', cmax and AUC of oral and nasal routes were significantly different (p < 0.01). Relative bioavailability of the drug nasal preparation to the oral suspension was up to 1600.0 %. Further, the in vitro effect of the risperidone nasal gel on nasal mucociliary movement was also investigated using a toad palate model. The risperidone nasal formulation showed mild ciliotoxicity, but the adverse effect was temporary and reversible.


Assuntos
Antipsicóticos/administração & dosagem , Antagonistas dos Receptores de Dopamina D2/administração & dosagem , Sistemas de Liberação de Medicamentos , Absorção Nasal , Mucosa Nasal/metabolismo , Risperidona/administração & dosagem , Antagonistas do Receptor 5-HT2 de Serotonina/administração & dosagem , Administração Intranasal , Animais , Antipsicóticos/efeitos adversos , Antipsicóticos/sangue , Antipsicóticos/farmacocinética , Anuros , Disponibilidade Biológica , Cílios/efeitos dos fármacos , Cílios/metabolismo , Antagonistas dos Receptores de Dopamina D2/efeitos adversos , Antagonistas dos Receptores de Dopamina D2/sangue , Antagonistas dos Receptores de Dopamina D2/farmacocinética , Composição de Medicamentos , Géis , Técnicas In Vitro , Masculino , Mucosa Bucal/efeitos dos fármacos , Mucosa Bucal/metabolismo , Mucosa Nasal/efeitos dos fármacos , Palato , Distribuição Aleatória , Ratos Wistar , Risperidona/efeitos adversos , Risperidona/sangue , Risperidona/farmacocinética , Antagonistas do Receptor 5-HT2 de Serotonina/efeitos adversos , Antagonistas do Receptor 5-HT2 de Serotonina/sangue , Antagonistas do Receptor 5-HT2 de Serotonina/farmacocinética
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