Movatterモバイル変換


[0]ホーム

URL:


Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
Thehttps:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

NIH NLM Logo
Log inShow account info
Access keysNCBI HomepageMyNCBI HomepageMain ContentMain Navigation
pubmed logo
Advanced Clipboard
User Guide

Full text links

Elsevier Science full text link Elsevier Science Free PMC article
Full text links

Actions

Share

.2008 Jun;89(4):499-507.
doi: 10.1016/j.pbb.2008.02.003. Epub 2008 Feb 8.

The effects of two highly selective dopamine D3 receptor antagonists (SB-277011A and NGB-2904) on food self-administration in a rodent model of obesity

Affiliations

The effects of two highly selective dopamine D3 receptor antagonists (SB-277011A and NGB-2904) on food self-administration in a rodent model of obesity

Panayotis K Thanos et al. Pharmacol Biochem Behav.2008 Jun.

Abstract

In the current study, we examined the effect of the selective D(3) receptor antagonists SB-277011A and NGB 2904 on operant food self-administration (FSA) in Zucker obese and lean rats. Obese (Ob) and lean (Le) Zucker rats were maintained under a restricted feeding regimen (70% of ad-libitum rat chow) and were trained to lever press for food during daily, 2 hour fixed-ratio 4 (FR4) schedules. Once rats reached a stable baseline for FSA, they were injected with vehicle until a stable FSA criterion was achieved. Animals then received daily injections of different random doses of SB-277011A (3, 10, and 30 mg/kg i.p.), and NGB-2904 (0.3, 1 and 3 mg/kg i.p.). SB-277011A produced a significant decrease in both food intake and active lever responses in both Ob and Le rats. In contrast, NGB-2904 did not decrease food intake levels or lever presses for food in Ob and Le rats. These results suggest that along with its involvement in seeking behavior for drugs of abuse, the D(3) dopamine receptor may also be involved in seeking behavior for natural reinforcers such as food.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Mean (+SEM) number of grams of food intake per 2-h session, following injection of: vehicle, 3, 10 or 30 mg/kg of SB-277011A. □ Denotes significance between specific treatment relative to all others, ~denotes significance between 10 and 3 mg/kg in Ob rats and * denotes significance between Ob and Le rats at specific dose. The vehicle column data represent the average of the first (baseline), intermittent (between treatments) and last (after the last drug treatment) vehicle sessions.
Fig. 2
Fig. 2
Mean (+SEM) number of R (total and during time-out) and NR lever responses per 2-h session, following injection of: vehicle, 3, 10, or 30 mg/kg of SB-277011A. □ Denotes significance between specific treatment relative to all others, and * denotes significance between Ob and Le rats at specific dose. The vehicle column data represent the average of the first (baseline), intermittent (between treatments) and last (after the last drug treatment) vehicle sessions.
Fig. 3
Fig. 3
Mean (+SEM) number of grams of food intake per 2-h session, following injection of: vehicle, 0.3, 1, or 3 mg/kg of NGB-2904. □ Denotes significance between specific treatment relative to all others, and * denotes significance between Ob and Le rats at specific dose. The vehicle column data represent the average of the first (baseline), intermittent (between treatments) and last (after the last drug treatment) vehicle sessions.
Fig. 4
Fig. 4
Mean (+SEM) number of R (total and during time-out) and NR lever responses per 2-h session, following injection of: vehicle, 0.3, 1, or 3 mg/kg of NGB-2904. □ Denotes significance between specific treatment relative to all others, and * denotes significance between Ob and Le rats at specific dose. The vehicle column data represent the average of the first (baseline), intermittent (between treatments) and last (after the last drug treatment) vehicle sessions.
See this image and copyright information in PMC

Similar articles

See all similar articles

Cited by

See all "Cited by" articles

References

    1. Alonso-Galicia M, Brands MW, Zappe DH, Hall JE. Hypertension in obese Zucker rats. Role of angiotensin II and adrenergic activity. Hypertension. 1996;28:1047–54. - PubMed
    1. Andreoli M, Tessari M, Pilla M, Valerio E, Hagan JJ, Heidbreder CA. Selective antagonism at dopamine D3 receptors prevents nicotine-triggered relapse to nicotine-seeking behavior. Neuropsychopharmacology. 2003;28:1272–80. - PubMed
    1. Ashby CR, Jr, Paul M, Gardner EL, Heidbreder CA, Hagan JJ. Acute administration of the selective D3 receptor antagonist SB-277011A blocks the acquisition and expression of the conditioned place preference response to heroin in male rats. Synapse (New York NY) 2003;48:154–6. - PubMed
    1. Barrett AC, Miller JR, Dohrmann JM, Caine SB. Effects of dopamine indirect agonists and selective D1-like and D2-like agonists and antagonists on cocaine self-administration and food maintained responding in rats. Neuropharmacology. 2004;47(Suppl 1):256–73. - PubMed
    1. Berridge KC. Food reward: brain substrates of wanting and liking. Neurosci Biobehav Rev. 1996;20:1–25. - PubMed

Publication types

MeSH terms

Substances

Related information

Grants and funding

LinkOut - more resources

Full text links
Elsevier Science full text link Elsevier Science Free PMC article
Cite
Send To

NCBI Literature Resources

MeSHPMCBookshelfDisclaimer

The PubMed wordmark and PubMed logo are registered trademarks of the U.S. Department of Health and Human Services (HHS). Unauthorized use of these marks is strictly prohibited.


[8]ページ先頭

©2009-2025 Movatter.jp