ABSTRACT. Distribution patterns of corticotropin-releasing factor (CRF), [arginine 8 ]-vasopressin (AVP) and oxytocin (OXY) neurons were examined immunohistochemically in the female goat hypothalamus. The majority of the CRF immunoreactive (-IR) cells were located in the parvocellular part of the paraventricular nucleus (PVN) with smaller population found in the magnocellular part of the PVN. CRF-IR cells were also found in the suprachiasmatic nucleus, the preoptic area and around the fornix in the caudal part of the hypothalamus. AVP-and OXY-IR cells were similarly distributed in the hypothalamus. The majority of AVP-and OXY-IR cells were observed in the magnocellular part of PVN and the supraoptic nucleus. Smaller numbers of AVP-and OXY-IR cells were found in the parvocellular part of the PVN and lateral hypothalamic area. AVP-IR but not OXY-IR cells were located in the suprachiasmatic nucleus. CRF-IR fibers were concentrated in the external palisade zone of the median eminence (ME) with a few fibers found in the internal palisade zone of the ME, whereas AVP-and OXY-IR fibers were concentrated in the internal palisade zone of the ME with a few fibers found in the external zone. These results support the view that not only CRF but also AVP and OXY are released into the hypophysial portal blood and involved in the control of pituitary endocrine function in ruminant species. -KEY WORDS: [arginine 8 ]-vasopressin, corticotropin-releasing factor, oxytocin, paraventricular hypothalamic nucleus, supraoptic nucleus.J. Vet. Med. Sci. 59(8): 621-628, 1997 neuroendocrinological studies to reveal the intra-brain function of three neuropeptides in the manifestation of stress-related behavior. The Shiba goat, which is a Japanese indigenous breed of goat and its closed colony has been established [10], was used in this study because basic information necessary for neurophysiological studies is available [13,25,26,31,32].
MATERIALS AND METHODSSpecimen: Brain samples were obtained from four adult female Shiba goats (Capra hirucus). They were deeply anesthetized with 30 mg/kg sodium pentobarbital following systemic heparinization (5,000 units/head, i.v.), and then perfused bilaterally via the carotid arteries with 3 l of 0.9% NaCl (the first 1 l of saline contained 10 units/ml heparin), followed by 2.5 l of Zamboni's fixative (4% paraformaldehyde, 7% saturated picric acid in 0.1 M phosphate buffer, pH 7.4) [30].Following the perfusion, the head, from which the parietal bone was carefully removed, was put on the stereotaxic instrument for the goat [13]. The method for the stereotaxic approach was described in detail elsewhere [32]. After taking lateral X-ray photographs, reference needles were inserted into the brain vertically until they reached the basis cranii interna with predetermined distances horizontally from the inter-aural (IA) line according to the brain atlas for the Shiba goat [31]. The brain was carefully removed from the cranium and trimmed down to a block with sections parallel to the reference needles. The ...