排序方式: 共有5条查询结果,搜索用时 0 毫秒
1
1.
Francesca Cherubino Andreea Miszner Maria Daniela Renna Rachele Sangaletti Stefano Giovannardi Elena Bossi 《Cellular and molecular life sciences : CMLS》2009,66(23):3797-3808
The effects of three tricyclic antidepressants (TCAs) and two serotonin selective reuptake inhibitors (SSRIs) have been studied
with an electrophysiological approach on Xenopus laevis oocytes expressing the rat GABA (γ-Aminobutyric-acid) transporter rGAT1. All tested TCAs and SSRIs inhibit the GABA-associated
current in a dose-dependent way with low but comparable efficacy. The pre-steady-state and uncoupled currents appear substantially
unaffected. The efficacy of desipramine, but not of the other drugs, is strongly increased in the lysine-glutamate or -aspartate
mutants K448E and K448D. Comparison of I
max and K
0.5GABA in the absence and presence of desipramine showed that both parameters are reduced by the drug in the wild-type and in the
K448E mutant. This suggests an uncompetitive inhibition, in which the drug can bind only after the substrate, an explanation
in agreement with the lack of effects on the pre-steady-state and leak currents, and with the known structural data. 相似文献
2.
Riassunto Piccole quantità di acqua di mare causano una forte inibizione della fosforilazione ossidativa, mentre l'effetto sulla attività citocromossidasica è piuttosto modesto. L'ione responsabile di questo effetto è il Calcio.
This work has been supported in part by a grant of the National Institute of Health, U.S. Public Health Service (RG-6211) to the Laboratory of Comparative Anatomy. 相似文献
This work has been supported in part by a grant of the National Institute of Health, U.S. Public Health Service (RG-6211) to the Laboratory of Comparative Anatomy. 相似文献
3.
Non-redundant role of the long pentraxin PTX3 in anti-fungal innate immune response 总被引:15,自引:0,他引:15
Garlanda C Hirsch E Bozza S Salustri A De Acetis M Nota R Maccagno A Riva F Bottazzi B Peri G Doni A Vago L Botto M De Santis R Carminati P Siracusa G Altruda F Vecchi A Romani L Mantovani A 《Nature》2002,420(6912):182-186
Pentraxins are a superfamily of conserved proteins that are characterized by a cyclic multimeric structure. The classical short pentraxins, C-reactive protein (CRP) and serum amyloid P component (SAP), are acute-phase proteins produced in the liver in response to inflammatory mediators. Short pentraxins regulate innate resistance to microbes and the scavenging of cellular debris and extracellular matrix components. In contrast, long pentraxins have an unrelated, long amino-terminal domain coupled to the carboxy-terminal pentraxin domain, and differ, with respect to short pentraxins, in their gene organization, chromosomal localization, cellular source, and in their stimuli-inducing and ligand-recognition ability. To investigate the in vivo function of the long pentraxin PTX3, we generated mice deficient in Ptx3 by homologous recombination. Ptx3-null mice were susceptible to invasive pulmonary aspergillosis. Ptx3 binds selected microbial agents, including conidia of Aspergillus fumigatus, and we found that susceptibility of Ptx3-null mice was associated with defective recognition of conidia by alveolar macrophages and dendritic cells, as well as inappropriate induction of an adaptive type 2 response. Thus, the long pentraxin Ptx3 is a secreted pattern-recognition receptor that has a non-redundant role in resistance to selected microbial agents, in particular to the opportunistic fungal pathogen Aspergillus fumigatus. 相似文献
4.
5.
1