Localization and Characterization of Nitric Oxide Synthase in the Rat Suprachiasmatic Nucleus: Evidence for a Nitrergic Plexus in the Biological Clock

• Published in: Journal of neurochemistry 1997-02, Vol.68 (2), p.855-861
• Main Authors: Chen, Dong, Hurst, William J., Ding, Jian M., Faiman, Lia E., Mayer, Bernd, Gillette, Martha U.
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry and metabolism; Biological and medical sciences; Biological Clocks - physiology; Blotting, Western; Central nervous system; Circadian rhythms; Confocal microscopy; Fundamental and applied biological sciences. Psychology; Immunohistochemistry; Isoenzymes - analysis; Isoenzymes - chemistry; Isoenzymes - metabolism; Microscopy, Confocal; Nitric oxide synthase; Nitric Oxide Synthase - analysis; Nitric Oxide Synthase - chemistry; Nitric Oxide Synthase - metabolism; Rat; Rats; Rats, Inbred Strains; Suprachiasmatic nucleus; Suprachiasmatic Nucleus - chemistry; Suprachiasmatic Nucleus - enzymology; Vertebrates: nervous system and sense organs
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1046/j.1471-4159.1997.68020855.x

: Behavioral and electrophysiological evidence indicates that the biological clock in the hypothalamic suprachiasmatic nuclei (SCN) can be reset at night through release of glutamate from the retinohypothalamic tract and subsequent activation of nitric oxide synthase (NOS). However, previous studies using NADPH‐diaphorase staining or immunocytochemistry to localize NOS found either no or only a few positive cells in the SCN. By monitoring conversion of l‐[3H]arginine to l‐[3H]citrulline, this study demonstrates that extracts of SCN tissue exhibit NOS specific activity comparable to that of rat cerebellum. The enzymatic reaction requires the presence of NADPH and is Ca2+/calmodulin‐dependent. To distinguish the neuronal isoform (nNOS; type I) from the endothelial isoform (type III), the enzyme activity was assayed over a range of pH values. The optimal pH for the reaction was 6.7, a characteristic value for nNOS. No difference in nNOS levels was seen between SCN collected in day versus night, either by western blot or by enzyme activity measurement. Confocal microscopy revealed for the first time a dense plexus of cell processes stained for nNOS. These data demonstrate that neuronal fibers within the rat SCN express abundant nNOS and that the level of the enzyme does not vary temporally. The distribution and quantity of nNOS support a prominent regulatory role for this nitrergic component in the SCN.