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*Substance via MeSH
Endocrinology Vol. 142, No. 8 3457-3463
Copyright © 2001 by The Endocrine Society


ARTICLES

Evidence of an Orexigenic Role for Cocaine- and Amphetamine-Regulated Transcript after Administration into Discrete Hypothalamic Nuclei

C. R. Abbott, M. Rossi, A. M. Wren, K. G. Murphy, A. R. Kennedy, S. A. Stanley, A. N. Zollner, D. G. A. Morgan, I. Morgan, M. A. Ghatei, C. J. Small and S. R. Bloom

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-(55–102), on feeding when injected into discrete nuclei of the hypothalamus. Cocaine- and amphetamine-regulated transcript-(55–102) (0.04 nmol) elicited a delayed, but significant, increase in feeding in 24-h fasted rats after injection into the ventromedial nucleus (1–2 h, 261 ± 60% of control; P < 0.05) and arcuate nucleus (1–2 h, 225 ± 38% of control; P < 0.05) of the hypothalamus. Administration of a higher dose of cocaine- and amphetamine-regulated transcript-(55–102) (0.2 nmol) elicited a significant increase in feeding after injection into the ventromedial nucleus (1–2 h, 1253 ± 179% of control; P < 0.001), arcuate nucleus (1–2 h, 265 ± 43% of control; P < 0.05), paraventricular nucleus (2–4 h food intake, 186 ± 29% of control; P < 0.05), lateral hypothalamic area (2–4 h, 280 ± 34% of control; P < 0.001), anterior hypothalamic area (2–4 h, 252 ± 42% of control; P < 0.01), dorsomedial nucleus (2–4 h, 368 ± 29% of control;P < 0.001) and supraoptic nucleus (2–4 h, 212 ± 34% of control; P < 0.05) of the hypothalamus. Administration of cocaine- and amphetamine-regulated transcript-(55–102) into the third ventricle of the hypothalamus resulted in an inhibition in feeding [0–4 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-(55–102) 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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Copyright © 2001 by The Endocrine Society