Journal
FASEB JOURNAL
Volume 27, Issue 3, Pages 1275-1284Publisher
FEDERATION AMER SOC EXP BIOL
DOI: 10.1096/fj.12-217653
Keywords
fetal programming; high-fat diet; reward
Categories
Funding
- National Health and Medical Research Council of Australia
- Australian Postgraduate Award
- University of South Australia
- Healthy Development Adelaide
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Perinatal exposure to a maternal junk-food diet has been demonstrated to increase the preference for palatable diets in adult offspring. We aimed to determine whether this increased preference could be attributed to changes in mu-opioid receptor expression within the mesolimbic reward pathway. We report here that mRNA expression of the mu-opioid receptor in the ventral tegmental area (VTA) at weaning was 1.4-fold (males) and 1.9-fold (females) lower in offspring of junk-food (JF)-fed rat dams than in offspring of dams fed a standard rodent diet (control) (P<0.05). Administration of the opioid antagonist naloxone to offspring given a palatable diet postweaning significantly reduced fat intake in control offspring (males: 7.7 +/- 0.7 vs. 5.4 +/- 0.6 g/kg/d; females: 6.9 +/- 0.3 vs. 3.9 +/- 0.5g/kg/d; P<0.05), but not in male JF offspring (8.6 +/- 0.6 vs. 7.1 +/- 0.5g/kg/d) and was less effective at reducing fat intake in JF females (42.2 +/- 6.0 vs. 23.1 +/- 4.1% reduction, P<0.05). Similar findings were observed for total energy intake. Naloxone treatment did not affect intake of standard rodent feed in control or JF offspring. These findings suggest that exposure to a maternal junk-food diet results in early desensitization of the opioid system which may explain the increased preference for junk food in these offspring.-Gugusheff, J. R., Ong, Z. Y., Muhlhausler, B. S. A maternal junk-food diet reduces sensitivity to the opioid antagonist naloxone in offspring postweaning. FASEB J. 27, 1275-1284 (2013). www.fasebj.org
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