Nitric oxide synthase in the hypothalamic paraventricular nucleus of the female rat; organization of spinal projections and coexistence with oxytocin or vasopressin

• Published in: Brain research 2001-07, Vol.908 (1), p.10-24
• Main Authors: Nylén, Anders, Skagerberg, Gunnar, Alm, Per, Larsson, Bengt, Holmqvist, Bo, Andersson, Karl-Erik
• Format: Article
• Language: English
• Subjects: Animals; Benzofurans - pharmacokinetics; Biological and medical sciences; Cell Count; Efferent Pathways - cytology; Efferent Pathways - enzymology; Estrus - physiology; Female; Fluorescent Dyes - pharmacokinetics; Functional Laterality - physiology; Fundamental and applied biological sciences. Psychology; Hypothalamus; Hypothalamus. Hypophysis. Epiphysis. Urophysis; Immunocytochemistry; Immunohistochemistry; Morphology. Functional localizations; Neuroendocrine; Neurons - cytology; Neurons - enzymology; Nitric oxide; Nitric Oxide - metabolism; Nitric Oxide Synthase - metabolism; Oxytocin - metabolism; Paraventricular Hypothalamic Nucleus - cytology; Paraventricular Hypothalamic Nucleus - enzymology; Rat; Rats; Rats, Sprague-Dawley; Sex Factors; Spinal Cord - cytology; Spinal Cord - enzymology; Spinal projections; Vasopressins - metabolism; Vertebrates: endocrinology
• ISSN: 0006-8993; 1872-6240
• DOI: 10.1016/S0006-8993(01)02539-2

We investigated the distributions and interrelations of neuronal nitric oxide (NO) synthase- (nNOS), oxytocin- (OT), and 8-arginine vasopressin- (AVP) immunoreactive (IR) neurons in the paraventricular nucleus (PVN), and the occurrence and distribution of nNOS spinally projecting neurons in the PVN of the female rat. Using double labelling immunohistochemistry, we mapped the distribution of nNOS-, OT- and AVP-immunoreactive (IR) neuronal cell bodies in the different parts of the PVN. About 80% of nNOS-IR cell bodies were magnocellular. About 30% of the nNOS-IR cell bodies were OT-IR, colocalization being most frequent in the rostral parts. In comparison, only ∼3% of all nNOS-IR cell bodies were AVP-IR, evenly distributed throughout the PVN. True Blue (TB), administered unilaterally into the spinal cord, disclosed that most spinally projecting cell bodies in the PVN were localized in caudal parts. Combined TB tracing and nNOS immunohistochemistry showed that ∼30% of spinally projecting neurons in the PVN were nNOS-IR, and that ∼40% of these were magnocellular. Ipsilateral nNOS spinal projections were about eight times more frequent than the contralateral nNOS projections. The study describes the detailed neuroanatomical organization of nNOS neurons coexpressing OT or AVP, and of nNOS spinally projecting neurons within defined parts of the PVN. In contrast to the paraventriculo-spinal system in general, we show that the nNOS paraventriculo-spinal pathway to a large extent originates in magnocellular cell bodies. The results suggest that NO is an important messenger in the paraventriculo-spinal pathway that may in part act in concert with OT.