Sex and menstrual cycle effects on progressive ratio measures of cocaine self-administration in cynomolgus monkeys

被引:46
作者
Mello, Nancy K. [1 ]
Knudson, Inge M. [1 ]
Mendelson, Jack H. [1 ]
机构
[1] Harvard Univ, Sch Med, McLean Hosp, Alcohol & Drug Abuse Res Ctr, Belmont, MA 02478 USA
关键词
menstrual cycle; ovarian steroid hormone; cocaine self-administration; progressive ratio schedule; sex effects;
D O I
10.1038/sj.npp.1301314
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Fluctuations in ovarian steroid hormones across the menstrual/estrous cycle influence the abuse-related effects of acute cocaine administration in women and chronic cocaine self-administration in rodents, but there have been no comparable studies in non-human primates. The interactions among sex, menstrual cycle phase, and cocaine self-administration (0.0032, 0.01, and 0.032 mg/kg/injection (inj)) under a progressive ratio schedule were investigated in four female and two male cynomolgus monkeys. Females were given unrestricted access to cocaine across 54 menstrual cycles, and males were studied over 23 pseudo-cycles of 30 days duration. Ovulatory cycles were defined by luteal phase elevations in progesterone and 44 cycles were ovulatory. During ovulatory menstrual cycles, females reached significantly higher progressive ratio break points than males at all three unit doses of cocaine (P<0.001). During anovulatory cycles, females also reached significantly higher break points than males for 0.032 mg/kg/inj cocaine (P<0.01). Progressive ratio break points for cocaine (0.01 and 0.032 mg/kg/inj) did not vary significantly as a function of ovarian steroid hormone levels during the follicular and the luteal phase of ovulatory menstrual cycles, or during anovulatory cycles. Progressive ratio break points for 0.0032 mg/kg/inj cocaine were significantly higher during the follicular phase than during the late luteal phase (P<0.05-0.001). There were no systematic changes in progressive ratio break points in male pseudo-cycles. Significant cocaine dose-related sex differences were observed, but no consistent changes in cocaine self-administration as a function of menstrual cycle phase, or levels of estradiol and progesterone, were detected in female cynomolgus monkeys.
引用
收藏
页码:1956 / 1966
页数:11
相关论文
共 64 条
  • [1] Usefulness of the monkey model to investigate the role of soy in postmenopausal women's health
    Appt, SE
    [J]. ILAR JOURNAL, 2004, 45 (02) : 200 - 211
  • [2] A critique of fixed and progressive ratio schedules used to examine the neural substrates of drug reinforcement
    Arnold, JM
    Roberts, DCS
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1997, 57 (03) : 441 - 447
  • [3] The cynomolgus monkey (Macaca fascicularis) is the best animal model for the study of steroid glucuronidation
    Barbier, O
    Bélanger, A
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2003, 85 (2-5) : 235 - 245
  • [4] Gender differences in dopaminergic function in striatum and nucleus accumbens
    Becker, JB
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1999, 64 (04) : 803 - 812
  • [5] Gender differences in the behavioral responses to cocaine and amphetamine - Implications for mechanisms mediating gender differences in drug abuse
    Becker, JB
    Molenda, H
    Hummer, DL
    [J]. BIOLOGICAL BASIS OF COCAINE ADDICTION, 2001, 937 : 172 - 187
  • [6] Bowman BP, 1999, J PHARMACOL EXP THER, V290, P1316
  • [7] Effect of baclofen on cocaine self-administration in rats reinforced under fixed-ratio 1 and progressive-ratio schedules
    Brebner, K
    Phelan, R
    Roberts, DCS
    [J]. PSYCHOPHARMACOLOGY, 2000, 148 (03) : 314 - 321
  • [8] Effect of gonadectomy and gonadal hormone replacement on cocaine self-administration in female and male rats
    Caine, SB
    Bowen, CA
    Yu, G
    Zuzga, D
    Negus, SS
    Mello, NK
    [J]. NEUROPSYCHOPHARMACOLOGY, 2004, 29 (05) : 929 - 942
  • [9] Sex and estrogen influence drug abuse
    Carroll, ME
    Lynch, WJ
    Roth, ME
    Morgan, AD
    Cosgrove, KP
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2004, 25 (05) : 273 - 279
  • [10] CHANNING CP, 1977, P SOC EXP BIOL MED, V155, P615