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10.1016/0165-5728(96)00083-5

http://scihub22266oqcxt.onion/10.1016/0165-5728(96)00083-5
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8784266!ä!8784266

suck abstract from ncbi


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pmid8784266      J+Neuroimmunol 1996 ; 68 (1-2): 101-8
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  • Interferon-gamma induced type I nitric oxide synthase activity inhibits viral replication in neurons #MMPMID8784266
  • Komatsu T; Bi Z; Reiss CS
  • J Neuroimmunol 1996[Aug]; 68 (1-2): 101-8 PMID8784266show ga
  • Type I NOS expression increases in OB neurons during VSV infection. Immunocytochemical staining of NB41A3 cells indicates constitutive expression of interferon (IFN)-gamma receptor and type I NOS. IFN-gamma treatment of NB41A3 cells increased NO production and type I NOS protein. In vitro replication of VSV, polio virus type I, and Herpes Simplex virus type I (HSV-1) is significantly inhibited by IFN-gamma induced type I NOS and antagonized by NOS inhibitors. In contrast, while IFN-gamma treatment inhibited influenza and Sindbis virus replication, a different pathway(s) was involved. The isoform-selective NOS inhibitor. 7-nitroindazole (7NI) was used to treat mice, resulting in a 10-fold higher titer of virus in brain homogenates, and abrogated the recovery-promoting effect of interleukin-12 treatment. Thus, IFN-gamma induced type I NOS activity may play an important role in host immunity against neurotropic viral infections.
  • |Animals[MESH]
  • |Astrocytoma[MESH]
  • |Base Sequence[MESH]
  • |Herpesvirus 1, Human/physiology[MESH]
  • |Interferon-gamma/*pharmacology[MESH]
  • |Macrophages/enzymology/immunology[MESH]
  • |Mice[MESH]
  • |Molecular Sequence Data[MESH]
  • |Neuroblastoma[MESH]
  • |Neurons/chemistry/*enzymology/*virology[MESH]
  • |Nitric Oxide Synthase/immunology/*metabolism[MESH]
  • |Nitric Oxide/biosynthesis[MESH]
  • |Poliovirus/physiology[MESH]
  • |Receptors, Interferon/analysis[MESH]
  • |Tumor Cells, Cultured/enzymology/immunology[MESH]
  • |Up-Regulation/immunology[MESH]
  • |Vesicular stomatitis Indiana virus/physiology[MESH]


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