1983
DOI: 10.1159/000123518
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Deficits in Drinking and Vasopressin Secretion after Lesions of the Nucleus medianus

Abstract: The effects of ablation of the nucleus medianus on drinking and vasopressin secretion were studied in male Long-Evans rats. The amount of water drunk in 1 h was assessed after subcutaneous injection of 5.8% NaCl (13.34 mosm/kg) or of angiotensin II (1.5 mg/kg). In a separate test with no water available, plasma vasopressin was measured 15 min after the above dose hypertonic saline. Ablation of the nucleus medianus, or the dorsal and anterior portions of the nucleus medianus, blocked drinking to hypertonic sali… Show more

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Cited by 177 publications
(71 citation statements)
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(4 reference statements)
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“…Moreover, the All receptors localized in this study correspond with many of the sites at which the peptide is known to exert behavioral, endocrine, or physiological actions. For example, sites involved in the drinking response to All, including the subfornical organ (58), organum vasculosum of the lamina terminalis (59), medial preoptic area (60), and median-preoptic nucleus (61), all contained moderate to high densities of angiotensin receptors. A neural pathway for angiotensin-mediated drinking has been defined by injections into subfornical organ of tritiated amino acids (62,63) or horseradish-peroxidase (64) and central lesion experiments (65).…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, the All receptors localized in this study correspond with many of the sites at which the peptide is known to exert behavioral, endocrine, or physiological actions. For example, sites involved in the drinking response to All, including the subfornical organ (58), organum vasculosum of the lamina terminalis (59), medial preoptic area (60), and median-preoptic nucleus (61), all contained moderate to high densities of angiotensin receptors. A neural pathway for angiotensin-mediated drinking has been defined by injections into subfornical organ of tritiated amino acids (62,63) or horseradish-peroxidase (64) and central lesion experiments (65).…”
Section: Discussionmentioning
confidence: 99%
“…Additional afferent and efferent connectivity with neurons in hypothalamic and brain stem centers provide possible circuits whereby MnPO neurons can influence several aspects of homeostasis such as hydromineral and cardiovascular regulation, salt appetite, and sleep-waking behavior (Johnson et al 1996;McKinley et al 1996;Suntsova et al 2002). Indeed major disruptions to homeostasis can be noted as a consequence of structural or chemical lesions focused on MnPO and the neighboring periventricular tissues (e.g., Bealer 2000; Cunningham et al 1991;Gardiner et al 1985Gardiner et al , 1986Mangiapane et al 1983;Yasuda et al 2000).…”
Section: Introductionmentioning
confidence: 99%
“…Lesions of the MnPO disrupt the drinking behavior in response to hyperosmolality, ANG II and hypovolemia (Mangiapane et al, 1983;Cunningham et al, 1991;Cunningham et al, 1992), attenuate vasopressin secretion during increase plasma osmolality and ANG II levels (Mangiapane et al, 1983;, and blunt centrally mediated pressor responses to hypertonic saline and ANG II (O'Neill and Brody, 1987;Yasuda et al, 2000). Each of the aforementioned stimuli increase Fos immunoreactivity, a marker of synaptic activation, in MnPO neurons (Oldfield et al, 1994;Larsen and Mikkelsen, 1995;Potts et al, 1999).…”
Section: Introductionmentioning
confidence: 99%