Pineal nitric oxide synthase, but not heme oxygenase, mRNA is suppressed by continuous exposure to light

被引:3
作者
Jacobs, RA
Schaad, NC
Vanecek, J
Leaver, S
Aubry, JM
Korf, HW
Dahia, PLM
Chew, SL
Grossman, AB
机构
[1] St Bartholomews Hosp, Dept Endocrinol, London EC1A 7BE, England
[2] Pharm Interhosp Cote, CH-1110 Morges, Switzerland
[3] Acad Sci Czech Republ, Inst Physiol, Prague, Czech Republic
[4] Univ Frankfurt Klinikum, D-60599 Frankfurt, Germany
来源
MOLECULAR BRAIN RESEARCH | 1999年 / 70卷 / 02期
基金
英国惠康基金;
关键词
pineal; nitric oxide; nitric oxide synthase; heme oxygenase; carbon monoxide; RT-PCR; light dark cycle;
D O I
10.1016/S0169-328X(99)00156-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have previously shown that exposure of rats to constant light (LL) induced a decrease in NO synthase (NOS) activity in the pineal gland. We report here that the use of the sensitive technique of RT-PCR has demonstrated that mRNA for neuronal NOS is present in the pineal, and that it is photoneurally regulated. There was a marked decrease in pineal neuronal NOS mRNA levels in continuous light conditions, similar to the changes seen in NOS enzyme activity. Inducible NOS was not present in the pineal, and there was evidence that the photoregulatable form was not endothelial NOS. The mRNA for two isoforms of heme oxygenase, the enzyme responsible for the generation of the putative neuromodulator carbon monoxide, was also present in the pineal, but neither isoform was photoregulated. Using immunodetection, it was not possible to identify the presence of NOS protein, other than to a minimal extent, even though NOS activity was clearly present. NADPH-diaphorase staining and in situ hybridization were carried out in an attempt to identify the precise location of neuronal NOS message. A strong NADPH-diaphorase reaction was present in sympathetic nerve fibers of the pineal, but pinealocytes showed no or only very weak labelling. In situ hybridization was also unable to identify neuronal NOS message in pinealocytes. These data thus also suggest the possible presence of a pineal-specific NOS isoenzyme. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:264 / 272
页数:9
相关论文
共 29 条
[1]  
Altschul Stephen F., J MOL BIOL, V215, P403, DOI [10.1016/S0022-2836(05)80360-2, DOI 10.1016/S0022-2836(05)80360-2]
[2]   CORTICOTROPIN-RELEASING FACTOR AND VASOPRESSIN MESSENGER-RNA LEVELS IN ROMAN HIGH-AVOIDANCE AND LOW-AVOIDANCE RATS - RESPONSE TO OPEN-FIELD EXPOSURE [J].
AUBRY, JM ;
BARTANUSZ, V ;
DRISCOLL, P ;
SCHULZ, P ;
STEIMER, T ;
KISS, JZ .
NEUROENDOCRINOLOGY, 1995, 61 (02) :89-97
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   LOCALIZATION OF NITRIC-OXIDE SYNTHASE INDICATING A NEURAL ROLE FOR NITRIC-OXIDE [J].
BREDT, DS ;
HWANG, PM ;
SNYDER, SH .
NATURE, 1990, 347 (6295) :768-770
[5]   NITRIC-OXIDE SYNTHASE PROTEIN AND MESSENGER-RNA ARE DISCRETELY LOCALIZED IN NEURONAL POPULATIONS OF THE MAMMALIAN CNS TOGETHER WITH NADPH DIAPHORASE [J].
BREDT, DS ;
GLATT, CE ;
HWANG, PM ;
FOTUHI, M ;
DAWSON, TM ;
SNYDER, SH .
NEURON, 1991, 7 (04) :615-624
[6]   ISOLATION OF NITRIC-OXIDE SYNTHETASE, A CALMODULIN-REQUIRING ENZYME [J].
BREDT, DS ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (02) :682-685
[7]   NITRIC-OXIDE MODULATES ENDOGENOUS DOPAMINE RELEASE IN BOVINE RETINA [J].
BUGNON, O ;
SCHAAD, NC ;
SCHORDERET, M .
NEUROREPORT, 1994, 5 (04) :401-404
[8]   AN ALTERNATIVELY SPLICED HUMAN INSULIN-LIKE GROWTH-FACTOR-I TRANSCRIPT WITH HEPATIC TISSUE EXPRESSION THAT DIVERTS AWAY FROM THE MITOGENIC IBE1 PEPTIDE [J].
CHEW, SL ;
LAVENDER, P ;
CLARK, AJL ;
ROSS, RJM .
ENDOCRINOLOGY, 1995, 136 (05) :1939-1944
[9]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[10]   NITRIC-OXIDE MODULATES THE RELEASE OF CORTICOTROPIN-RELEASING HORMONE FROM THE RAT HYPOTHALAMUS INVITRO [J].
COSTA, A ;
TRAINER, P ;
BESSER, M ;
GROSSMAN, A .
BRAIN RESEARCH, 1993, 605 (02) :187-192