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Endocrine Unit, Imperial College School of Medicine, Hammersmith Hospital, London, United Kingdom W12 ONN
Address all correspondence and requests for reprints to: Prof. S. R. Bloom, Imperial College School of Medicine Endocrine Unit, Hammersmith Hospital, London, United Kingdom W12 0NN.
Cocaine- and amphetamine-regulated transcript is expressed in hypothalamic regions involved in the central control of food intake. Previous data have implicated cocaine- and amphetamine-regulated transcript as an anorectic peptide. We studied the effect of the active fragment of cocaine- and amphetamine-regulated transcript, cocaine- and amphetamine-regulated transcript-(55102), on feeding when injected into discrete nuclei of the hypothalamus. Cocaine- and amphetamine-regulated transcript-(55102) (0.04 nmol) elicited a delayed, but significant, increase in feeding in 24-h fasted rats after injection into the ventromedial nucleus (12 h, 261 ± 60% of control; P < 0.05) and arcuate nucleus (12 h, 225 ± 38% of control; P < 0.05) of the hypothalamus. Administration of a higher dose of cocaine- and amphetamine-regulated transcript-(55102) (0.2 nmol) elicited a significant increase in feeding after injection into the ventromedial nucleus (12 h, 1253 ± 179% of control; P < 0.001), arcuate nucleus (12 h, 265 ± 43% of control; P < 0.05), paraventricular nucleus (24 h food intake, 186 ± 29% of control; P < 0.05), lateral hypothalamic area (24 h, 280 ± 34% of control; P < 0.001), anterior hypothalamic area (24 h, 252 ± 42% of control; P < 0.01), dorsomedial nucleus (24 h, 368 ± 29% of control;P < 0.001) and supraoptic nucleus (24 h, 212 ± 34% of control; P < 0.05) of the hypothalamus. Administration of cocaine- and amphetamine-regulated transcript-(55102) into the third ventricle of the hypothalamus resulted in an inhibition in feeding [04 h (0.4 nmol), 33 ± 13% control; P < 0.001], but was associated with marked abnormalities in behavior, which may have interfered with feeding. These behavioral abnormalities were not observed after the administration of cocaine- and amphetamine-regulated transcript-(55102) directly into the arcuate nucleus. These data suggest that cocaine- and amphetamine-regulated transcript may play an orexigenic role in the hypothalamic feeding circuitry.
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