NITRIC-OXIDE SYNTHASE-CONTAINING NEURONS IN THE HUMAN HYPOTHALAMUS - REDUCED NUMBER OF IMMUNOREACTIVE CELLS IN THE PARAVENTRICULAR NUCLEUS OF DEPRESSIVE PATIENTS AND SCHIZOPHRENICS
Hg. Bernstein et al., NITRIC-OXIDE SYNTHASE-CONTAINING NEURONS IN THE HUMAN HYPOTHALAMUS - REDUCED NUMBER OF IMMUNOREACTIVE CELLS IN THE PARAVENTRICULAR NUCLEUS OF DEPRESSIVE PATIENTS AND SCHIZOPHRENICS, Neuroscience, 83(3), 1998, pp. 867-875
The neuroanatomical distribution of nitric oxide synthase-immunoreacti
ve neurons was investigated in post moi rem hypothalami of 10 patients
suffering from schizophrenia, eight patients with depression and 13 m
atched control cases. Neuronal nitric oxide synthase containing nerve
cells were detected in several hypothalamic nuclei including the media
l preoptic region, the ventromedial, infundibular and suprachiasmatic
nuclei and the lateral hypothalamus. The vast majority of hypothalamic
nitric oxide synthase-immunoreactive neurons was found to be located
in the paraventricular nucleus. Both magno and parvocellular paraventr
icular neurons contained the enzyme. A small subset of immunoreactive
parvocellular paraventricular neurons co-expresses corticotropin-relea
sing hormone. The supraoptic nucleus did not contain nitric oxide synt
hase-immunoreactive neurons. Cell counts of paraventricular nitric oxi
de synthase-positive neurons in controls, schizophrenics and depressed
patients revealed a statistically significant reduction of cell densi
ty in the right paraventricular nucleus of depressed patients and schi
zophrenics as compared to controls. The total amount of nitric oxide s
ynthase-immunoreactive paraventricular neurons was smaller in depressi
ve and schizophrenic patients than in normal cases. The putative patho
physiologic significance of the reduced expression of paraventricular
nitric oxide synthase in depressive patients might be related to the s
upposed regulatory function of nitric oxide in the release of corticot
ropin-releasing hormone and arginine-vasopressin and/or oxytocin, whic
h have been reported to be over-expressed in the so-called endogenous
psychoses, especially in depression. (C) 1998 IBRO. Published by Elsev
ier Science Ltd.