A rapid transient synthesis of nitric oxide (NO) by a constitutively expressed type IINO synthase in the guinea-pig suprachiasmatic nucleus

Citation
Sj. Starkey et al., A rapid transient synthesis of nitric oxide (NO) by a constitutively expressed type IINO synthase in the guinea-pig suprachiasmatic nucleus, BR J PHARM, 134(5), 2001, pp. 1084-1092
Citations number
66
Categorie Soggetti
Pharmacology & Toxicology
Journal title
BRITISH JOURNAL OF PHARMACOLOGY
ISSN journal
00071188 → ACNP
Volume
134
Issue
5
Year of publication
2001
Pages
1084 - 1092
Database
ISI
SICI code
0007-1188(200111)134:5<1084:ARTSON>2.0.ZU;2-4
Abstract
1 We have measured extracellular NO/NO2- concentrations in guinea-pig supra chiasmatic nucleus (SCN) brain slices using fast cyclic voltammetry. A rapi d and transient signal equivalent to 2.2 +/-0.2 muM NO/NO2- (mean +/-s.e.me an, n=13) was detected at 1.26 V, the peak oxidation potential for NO, foll owing local electrical stimulation (five pulses of 0.1 ms duration at 100 H z, delivered every 5 min). 2 The NO/NO2- signal was inhibited by the non-selective nitric oxide syntha se (NOS) inhibitors L-NAME, L-NMMA and the highly selective type II NOS (iN OS) inhibitor 1400 W (Garvey et al., 1997) in a concentration-dependent man ner. IC50 values were 229 muM (65-801, n=3, geomean and 95% confidence inte rvals (C.I.)), 452 nM (88-2310, n=5), and 14.2 muM (3.6=54.4, n=5), with ma ximum inhibitions of 82.8 +/-6.7, 46.0 +/-8.1, and 90.6 +/-3.6%, respective ly. 3 Exposure of the slices to the protein synthesis inhibitor cyclohexamide o r the inhibitor of type II NOS induction dexamethasone immediately followin g slice cutting, and for a subsequent 4-5 h, did not inhibit the NO/NO2- si gnal. 4 The evoked NO/NO2- signal was not reduced following 6 h perfusion in Ca2-free media, consistent with a Ca2+-independent type II NOS activity. 5 PCR for type II NOS revealed the presence of this isotype in the SCN, eve n immediately following removal of the brain. 6 These studies provide the first evidence to suggest a functional, constit utively-active type II NOS within the brain of normal, healthy adult animal s, and add type II NOS to the multiple isotypes of NO synthase playing a ro le within the mammalian SCN.