TY - JOUR
T1 - Changes in body weight and food-related behaviour induced by destruction of the ventral or dorsal noradrenergic bundle in the rat
AU - Sahakian, B.J
AU - Winn, P.
AU - Robbins, T.W.
AU - Deeley, R.J.
AU - Everitt, B.J.
AU - Dunn, L.T.
AU - Wallace, M.
AU - James, W.P.T.
PY - 1983/12/31
Y1 - 1983/12/31
N2 - Three experiments contrasted the effects of 6-hydroxydopamine-induced lesions of the ventral noradrenergic and dorsal noradrenergic projections, predominantly to hypothalamus and cortex, respectively, upon body weight changes and food-related behaviour in the rat. In general, ventral noradrenergic bundle lesions enhanced weight gain and these effects were exaggerated by the provision of palatable cheese to the standard chow diet. In contrast, lesions of the dorsal noradrenergic bundle produced minor changes in body weight. Associated with the effects of ventral noradrenergic bundle lesions were hyperphagia, enhanced suppression of intake of food adulterated with quinine, (at high concentration), a small attenuation of food neophobia, and enhanced acquisition, but not performance, of the eating response to tail-pinch stimulation. These ventral noradrenergic bundle lesions failed to alter basal activity levels, amphetamine anorexia or the diurnal pattern of eating or activity. In contrast, lesions of the dorsal noradrenergic bundle did not produce either hyperphagia or enhanced rejection of food adulterated with quinine. However, there was a strong attenuation of food neophobia and a retarded acquisition (but unimpaired performance) of eating in response to tail-pinch stimulation. The results are discussed in connection with previous studies of ventral and dorsal noradrenergic bundle lesions, with the effects of ventromedial hypothalamic lesions and with the underlying behavioural and physiological processes that mediate these contrasting effects of different neuroanatomical patterns of central noradrenaline depletion. © 1983.
AB - Three experiments contrasted the effects of 6-hydroxydopamine-induced lesions of the ventral noradrenergic and dorsal noradrenergic projections, predominantly to hypothalamus and cortex, respectively, upon body weight changes and food-related behaviour in the rat. In general, ventral noradrenergic bundle lesions enhanced weight gain and these effects were exaggerated by the provision of palatable cheese to the standard chow diet. In contrast, lesions of the dorsal noradrenergic bundle produced minor changes in body weight. Associated with the effects of ventral noradrenergic bundle lesions were hyperphagia, enhanced suppression of intake of food adulterated with quinine, (at high concentration), a small attenuation of food neophobia, and enhanced acquisition, but not performance, of the eating response to tail-pinch stimulation. These ventral noradrenergic bundle lesions failed to alter basal activity levels, amphetamine anorexia or the diurnal pattern of eating or activity. In contrast, lesions of the dorsal noradrenergic bundle did not produce either hyperphagia or enhanced rejection of food adulterated with quinine. However, there was a strong attenuation of food neophobia and a retarded acquisition (but unimpaired performance) of eating in response to tail-pinch stimulation. The results are discussed in connection with previous studies of ventral and dorsal noradrenergic bundle lesions, with the effects of ventromedial hypothalamic lesions and with the underlying behavioural and physiological processes that mediate these contrasting effects of different neuroanatomical patterns of central noradrenaline depletion. © 1983.
KW - dopamine
KW - dorsal/ventral noradrenergic bundle
KW - 5-HT
KW - serotonin
KW - high performance liquid chromatography
KW - 6-hydroxydopamine
KW - ventral medial hypothalamus
UR - http://www.scopus.com/inward/record.url?scp=0021015203&partnerID=8YFLogxK
UR - https://www.sciencedirect.com/journal/neuroscience
U2 - 10.1016/0306-4522(83)90122-7
DO - 10.1016/0306-4522(83)90122-7
M3 - Article
C2 - 6607427
AN - SCOPUS:0021015203
SN - 0306-4522
VL - 10
SP - 1405
EP - 1420
JO - Neuroscience
JF - Neuroscience
IS - 4
ER -