In the adult central nervous system, nitric oxide (NO) is formed from L- arginine by the so-called constitutive or type I NO synthase (NOS-I155). However, expression of NOS-1155 immunoreactivity and activity was low or not detectable in developing mouse and rat brain. NOS-I155 was sharply induced coincident with the onset of synaptogenesis in specific brain regions. This was followed by a second phase in which total NOS-I155 expression decreased both in specific cell populations and in the total synaptosomal subcellular fraction. Furthermore, two putative variants of NOS-I were transiently observed: an NOS-I-immunoreactive protein with increased electrophoretic mobility (NOS-I144) and a transient hypersensitivity of NOS-I155 to the competitive substrate inhibitor N(ω)-nitro-L-arginine. It is concluded that NOS-I expression is not constitutive but locally induced. In the central nervous system, this regionally specific, bipbasic pattern of postnatal NOS-I induction is consistent with a role for NO in synaptogenesis and synaptic plasticity.
|Original language||English (US)|
|Number of pages||8|
|State||Published - Jan 1 1995|
All Science Journal Classification (ASJC) codes
- Molecular Biology