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-I-
155) However, expression of NOS-I-155 immunoreactivity and activity wa
s low or not detectable in developing mouse and rat brain. NOS-I-155 w
as sharply induced coincident with the onset of synaptogenesis in spec
ific brain regions, This was followed by a second phase in which total
NOS-I-155 expression decreased both in specific cell populations and
in the total synaptosomal subcellular fraction, Furthermore, two putat
ive variants of NOS-I were transiently observed: an NOS-I-immunoreacti
ve protein with increased electrophoretic mobility (NOS-I-144) and a t
ransient hypersensitivity of NOS-I-155 to the competitive substrate in
hibitor N-omega-nitro-L-arginine. It is concluded that NOS-I expressio
n is not constitutive but locally induced. In the central nervous syst
em, this regionally specific, biphasic pattern of postnatal NOS-I indu
ction is consistent with a role for NO in synaptogenesis and synaptic
plasticity.