作者: Ira B. Black , Tong Hyub Joh , Donald J. Reis
DOI: 10.1016/0006-8993(74)90775-6
关键词: Ganglion 、 Specific antibody 、 Depolarization 、 Postsynaptic potential 、 Superior cervical ganglion 、 Internal medicine 、 Endocrinology 、 Tyrosine hydroxylase 、 Biology 、 Enzyme 、 Ontogeny
摘要: Abstract The developmental increase in tyrosine hydroxylase (T-OH) activity the superior cervical ganglion (SCG) from mice and rats was studied using a specific antibody to enzyme. Immunotitration studies demonstrated that ontogenetic rise T-OH entirely attributable an enzyme molecule numbers, not activation of pre-existent immunotitration suggested neonatal adult molecules were immunochemically similar. Furthermore, enzymes had equivalent thermo-stabilities, implying physicochemical similarity. These observations suggest there are no structural differences between T-OH, maturation does involve appearance different species molecules. postnatal accumulation protein prevented by decentralization or pharmacologic ganglionic blockade. Consequently, release presynaptic acetycholine postsynaptic depolarization appear regulate accretion protein.