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<title>Saudi Pharmaceutical Journal August 2024</title>
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<place><placeTerm type="text">Arab Saudi</placeTerm></place>
<publisher>University of Jeddah</publisher>
<dateIssued>2024</dateIssued>
<issuance>monographic</issuance>
<edition>August 2024</edition>
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<languageTerm type="text">Indonesia</languageTerm>
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<note>ABSTRACT
Background: The recent global increase in obesity rates, coupled with excessive palatable food (PF) consumption,
has become a serious societal concern. Literature indicates that rewarding PF, especially upon cessation, can lead

to overeating, binge eating, and compulsive eating, potentially resulting in obesity. Challenges in dietary par-
adigms, alongside limitations in approved treatments for eating disorders and anti-obesity medications, under-
score the need to explore novel targets. In this context, &alpha;7nAChR (alpha-7 nicotinic acetylcholine receptor) may

serve as a promising therapeutic target in combating food dependence and obesity. The present study aims to
assess the role of &alpha;7nAChR in palatable food-induced dependence-like behaviors.
Method: The study involved male C57BL/6J mice exposed to three different feeding paradigms over 6 weeks to
induce obesity and food addiction. On day 43, palatable food was replaced with standard chow, and the mice
received treatments (vehicle, PNU-282987 [&alpha;7nAChR agonist], or methyllycaconitine citrate [MLA; &alpha;7nAChR
antagonist]). Addiction-like behaviors, including craving for palatable food, motivation-effort interaction tests,
and compulsive eating-like behavior, were measured during abstinence with and without treatment.
Results: The present study shows that chronic intermittent and continuous exposure to palatable food induces
craving, motivation, and effort interaction behaviors as well as compulsive eating-like behaviors in palatable
food-abstinent mice. Administration of the &alpha;7nAChR agonist, PNU-282987, significantly attenuated the craving
behavior only in mice continuously fed palatable food (reduced calorie intake from 63.19 % to 48.21 %; p =
0.0053). Also, PNU-282987 suppressed the effort behaviors in either intermittently or continuously fed mice
(significant reduction in the &Delta; number of active events per minute; p-values = 0.038 and 0.0098, respectively).
However, it attenuated the compulsive-like eating behavior exclusively in the continuously fed group (p =
0.0433). Active and total interaction efforts were reversed by the MLA. These findings indicate the involvement of &alpha;7nAChR in dependence-like behaviors toward palatable food in mice.</note>
<subject authority=""><topic>Obesity</topic></subject>
<subject authority=""><topic>Food addiction</topic></subject>
<subject authority=""><topic>Palatable food</topic></subject>
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<physicalLocation>PERPUSTAKAAN SEKOLAH TINGGI ILMU KESEHATAN SAMARINDA REPOSITORY</physicalLocation>
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<sublocation>Perpus.Akfarsam (Jurnal Farmasi Internasional)</sublocation>
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