TY - JOUR
T1 - mRNA transcription determines the lag period for the induction of pineal melatonin synthesis in the Syrian hamster pineal gland
AU - Gonzalez‐Brito, Aldo
AU - Troiani, Maureen E.
AU - Menendez‐Pelaez, Armando
AU - Delgado, Maria J.
AU - Reiter, Russel J.
PY - 1990/9
Y1 - 1990/9
N2 - The nocturnal pattern of Syrian hamster pineal melatonin synthesis is characterized by a 6–8 h lag period, followed by a late‐night, short‐duration peak in both N‐acetyltransferase (NAT) activity and melatonin content. Administration of cycloheximide (20 mg/kg body weight) given either at the time of lights out or 4 h into the dark phase to Syrian hamsters blocked the nocturnal increase in both pineal NAT activity and melatonin content. Actinomycin D (5 mg/kg body weight) prevented the nocturnal increase in both constituents only when it was administered at darkness onset, being significantly less effective when injected after 4 h of dark exposure. Reinduction of melatonin production by isoproterenol (2 mg/kg body weight) administration to acutely light‐exposed animals during late darkness was prevented by cycloheximide, but not by actinomycin D administration. The results suggest that whereas Syrian hamster pineal melatonin production requires protein synthesis both early and late in the dark phase, the transcription of a putative NAT‐related mRNA, which occurs only during the early night, seems to determine the lag period in melatonin synthesis and pineal responsiveness to β‐adrenergic receptor agonist stimulation.
AB - The nocturnal pattern of Syrian hamster pineal melatonin synthesis is characterized by a 6–8 h lag period, followed by a late‐night, short‐duration peak in both N‐acetyltransferase (NAT) activity and melatonin content. Administration of cycloheximide (20 mg/kg body weight) given either at the time of lights out or 4 h into the dark phase to Syrian hamsters blocked the nocturnal increase in both pineal NAT activity and melatonin content. Actinomycin D (5 mg/kg body weight) prevented the nocturnal increase in both constituents only when it was administered at darkness onset, being significantly less effective when injected after 4 h of dark exposure. Reinduction of melatonin production by isoproterenol (2 mg/kg body weight) administration to acutely light‐exposed animals during late darkness was prevented by cycloheximide, but not by actinomycin D administration. The results suggest that whereas Syrian hamster pineal melatonin production requires protein synthesis both early and late in the dark phase, the transcription of a putative NAT‐related mRNA, which occurs only during the early night, seems to determine the lag period in melatonin synthesis and pineal responsiveness to β‐adrenergic receptor agonist stimulation.
KW - actinomycin D
KW - cycloheximide
KW - isoproterenol
KW - nocturnal melatonin production
KW - β‐adrenergic receptors
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U2 - 10.1002/jcb.240440105
DO - 10.1002/jcb.240440105
M3 - Article
C2 - 2135399
AN - SCOPUS:0025012085
SN - 0730-2312
VL - 44
SP - 55
EP - 60
JO - Journal of Cellular Biochemistry
JF - Journal of Cellular Biochemistry
IS - 1
ER -