Divergent selection for pentobarbital-induced sedation times in mice

被引:6
|
作者
Stino, FKR [1 ]
Samaan, SS [1 ]
Kolta, MG [1 ]
Mizinga, KM [1 ]
Soliman, KFA [1 ]
机构
[1] Florida A&M Univ, Coll Pharm & Pharmaceut Sci, Tallahassee, FL 32307 USA
关键词
mice; selection; pentobarbital; heritabilities; sedation time;
D O I
10.1159/000028186
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Divergent selection for pentobarbital sedation-time response was practiced in mice for 9 generations. At the end of 9 generations of selection, the long-sedation-time line (LST) slept an average of 433 min; the short sedation time line (SST) slept an average of 29 min. The control line (C) slept an average of 71 min. These differences represent an almost 15-fold increase in sedation time for the LST compared to the SST line and a 6-fold increase compared to the C line. The SST line slept about 40% less than the C line after 9 generations of selection (measured in tenth generation progeny). Analysis of selection differentials and realized heritabilities indicated that selection response did not diminish after 9 generations of selection. Realized heritabilities for sedation time ranged from 0.43 to 0.83 for the LST line and from 0.55 to 0.81 for the SST line. Realized heritabilities did not decrease in magnitude due to selection progress, indicating that more progress can still be achieved. Comparing corrected (for environmental factors) to uncorrected heritabilities showed the importance of including a control line in selection experiments. Crossing of lines to study gene action responsible for this trait revealed that this trait was controlled by a number of genes with additive gene action without dominance, overdominance, epistasis, or maternal effects.
引用
收藏
页码:92 / 100
页数:9
相关论文
共 50 条
  • [21] INFLUENCE OF OZONE ON PENTOBARBITAL-INDUCED SLEEPING TIME IN MICE, RATS, AND HAMSTERS
    GRAHAM, JA
    MENZEL, DB
    MILLER, FJ
    ILLING, JW
    GARDNER, DE
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1981, 61 (01) : 64 - 73
  • [22] Effects of morphine on pentobarbital-induced responses in μ-opioid receptor knockout mice
    Park, Y
    Ho, IK
    Jang, CG
    Tanaka, S
    Ma, T
    Loh, HH
    Ko, KH
    BRAIN RESEARCH BULLETIN, 2001, 54 (05) : 527 - 531
  • [23] Pentobarbital-induced place aversion learning
    Lew, G
    Parker, LA
    ANIMAL LEARNING & BEHAVIOR, 1998, 26 (02): : 219 - 224
  • [24] MORPHINE ANTAGONIZES PENTOBARBITAL-INDUCED ANESTHESIA
    HORITA, A
    CARINO, MA
    YAMAWAKI, S
    NEUROPHARMACOLOGY, 1983, 22 (10) : 1183 - 1186
  • [25] Pentobarbital-induced place aversion learning
    Gilbert Lew
    Linda A. Parker
    Animal Learning & Behavior, 1998, 26 : 219 - 224
  • [26] PENTOBARBITAL-INDUCED CONFIGURATIONAL CHANGES AT SYNAPSE
    COOKE, CT
    NOLAN, TM
    DYSON, SE
    JONES, DG
    BRAIN RESEARCH, 1974, 76 (02) : 330 - 335
  • [27] SODIUM PENTOBARBITAL-INDUCED MUTATIONS IN THE HAMSTER
    ITO, T
    INGALLS, TH
    ARCHIVES OF ENVIRONMENTAL HEALTH, 1981, 36 (06): : 316 - 320
  • [28] Different effects of arecoline on ethanol- and pentobarbital-induced central suppression in mice
    Liang, Jian-Hui
    Sun, Yan-Ping
    Han, Rong
    Luo, Juan
    Chen, Feng
    Lawrence, Andrew John
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2006, 30 (09) : 164A - 164A
  • [29] Screening of Bangladeshi medicinal plants for their effects on pentobarbital-induced sleeping time in mice
    Chakma, T. K.
    Khan, M. T. H.
    Rahman, T.
    Choudhuri, M. S. K.
    Rajia, S.
    Alamgir, M.
    ARS PHARMACEUTICA, 2006, 47 (02) : 211 - 217
  • [30] THE EFFECTS OF METHAPYRILENE HYDROCHLORIDE ON HEPATOCARCINOGENICITY AND PENTOBARBITAL-INDUCED SLEEPING TIME IN RATS AND MICE
    BRENNAN, LM
    CREASIA, DA
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1982, 66 (02) : 252 - 258