Guidelines on nicotine dose selection for in vivo research

被引:655
作者
Matta, Shannon G.
Balfour, David J.
Benowitz, Neal L.
Boyd, R. Thomas
Buccafusco, Jerry J.
Caggiula, Anthony R.
Craig, Caroline R.
Collins, Allan C.
Damaj, M. Imad
Donny, Eric C.
Gardiner, Phillip S.
Grady, Sharon R.
Heberlein, Ulrike
Leonard, Sherry S.
Levin, Edward D.
Lukas, Ronald J.
Markou, Athina
Marks, Michael J.
McCallum, Sarah E.
Parameswaran, Neeraja
Perkins, Kenneth A.
Picciotto, Marina R.
Quik, Maryka
Rose, Jed E.
Rothenfluh, Adrian
Schafer, William R.
Stolerman, Ian P.
Tyndale, Rachel F.
Wehner, Jeanne M.
Zirger, Jeffrey M.
机构
[1] Univ Tennessee, Hlth Sci Ctr, Dept Pharmacol, Coll Med, Memphis, TN 38163 USA
[2] Univ Dundee, Sch Med, Dept Pharmacol & Neurosci, Dundee, Scotland
[3] Univ Calif San Francisco, Div Clin Pharmacol & Expt Therapeut, Dept Med, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Div Clin Pharmacol & Expt Therapeut, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
[5] Ohio State Univ, Dept Neurosci, Coll Med & Publ Hlth, Columbus, OH 43210 USA
[6] Med Coll Georgia, Dept Pharmacol, Augusta, GA 30912 USA
[7] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA 15260 USA
[8] Univ Calif San Diego, Neurobiol Sect, San Diego, CA 92103 USA
[9] Univ Colorado, Inst Behav Genet, Boulder, CO 80309 USA
[10] Virginia Commonwealth Univ, Med Coll Virginia, Dept Pharmacol & Toxicol, Richmond, VA 23298 USA
[11] Univ Calif Oakland, Tobacco Related Dis Res Program, Off President, Oakland, CA USA
[12] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[13] Univ Colorado, Hlth Sci Ctr, Dept Psychiat, Denver, CO 80262 USA
[14] Univ Colorado, Hlth Sci Ctr, Dept Pharmacol, Denver, CO 80262 USA
[15] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham, NC USA
[16] Barrow Neurol Inst, Div Neurobiol, Phoenix, AZ 85013 USA
[17] Univ Calif San Diego, Sch Med, Dept Psychiat, La Jolla, CA 92093 USA
[18] Parkinsons Inst, Sunnyvale, CA USA
[19] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA USA
[20] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
[21] Duke Univ, Med Ctr, Ctr Nicotine & Smoking Cessat Res, Durham, NC USA
[22] Kings Coll London, Inst Psychiat, Sech Behav Pharmacol, London WC2R 2LS, England
[23] Univ Toronto, Dept Pharmacol, Ctr Addict & Mental Hlth, Toronto, ON, Canada
基金
英国医学研究理事会;
关键词
human; nonhuman primate; rat; mouse; Drosophila; C; elegans; zebrafish; CONDITIONED PLACE PREFERENCE; HYPOTHALAMIC PARAVENTRICULAR NUCLEUS; INDUCED DOPAMINE RELEASE; INDUCED NOREPINEPHRINE SECRETION; ACETYLCHOLINE-RECEPTOR AGONIST; SELF-ADMINISTERED NICOTINE; SUBUNIT MESSENGER-RNAS; CENTRAL-NERVOUS-SYSTEM; TO-SAMPLE PERFORMANCE; AMINO-ACID-SEQUENCE;
D O I
10.1007/s00213-006-0441-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale: This review provides insight for the judicious selection of nicotine dose ranges and routes of administration for in vivo studies. The literature is replete with reports in which a dosaging regimen chosen for a specific nicotine-mediated response was suboptimal for the species used. In many cases, such discrepancies could be attributed to the complex variables comprising species-specific in vivo responses to acute or chronic nicotine exposure. Objectives: This review capitalizes on the authors' collective decades of in vivo nicotine experimentation to clarify the issues and to identify the variables to be considered in choosing a dosaging regimen. Nicotine dose ranges tolerated by humans and their animal models provide guidelines for experiments intended to extrapolate to human tobacco exposure through cigarette smoking or nicotine replacement therapies. Just as important are the nicotine dosaging regimens used to provide a mechanistic framework for acquisition of drug-taking behavior, dependence, tolerance, or withdrawal in animal models. Results: Seven species are addressed: humans, nonhuman primates, rats, mice, Drosophila, Caenorhabditis elegans, and zebrafish. After an overview on nicotine metabolism, each section focuses on an individual species, addressing issues related to genetic background, age, acute vs chronic exposure, route of administration, and behavioral responses. Conclusions: The selected examples of successful dosaging ranges are provided, while emphasizing the necessity of empirically determined dose-response relationships based on the precise parameters and conditions inherent to a specific hypothesis. This review provides a new, experimentally based compilation of species-specific dose selection for studies on the in vivo effects of nicotine.
引用
收藏
页码:269 / 319
页数:51
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