Ischemic but not thermal pain sensitivity varies across the menstrual cycle

被引:142
作者
Fillingim, RB
Maixner, W
Girdler, SS
Light, KC
Harris, B
Sheps, DS
Mason, GA
机构
[1] UNIV N CAROLINA,DENT RES CTR,CHAPEL HILL,NC 27599
[2] UNIV N CAROLINA,DEPT ENDODONT & PHARMACOL,CHAPEL HILL,NC 27599
[3] UNIV N CAROLINA,DEPT PSYCHIAT,CHAPEL HILL,NC 27599
[4] UNIV N CAROLINA,DEPT MED,CHAPEL HILL,NC 27599
来源
PSYCHOSOMATIC MEDICINE | 1997年 / 59卷 / 05期
关键词
thermal pain; ischemic pain; menstrual cycle; opioids; gonadal hormones;
D O I
10.1097/00006842-199709000-00008
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective and Method: Findings from both animal and human research suggest that pain sensitivity changes across the menstrual cycle; however, among humans the nature of these menstrual cycle effects remains unclear. The present study used a repeated-measures design to evaluate changes in thermal and ischemic pain responses during three phases of the menstrual cycle, midfollicular (postmenstrual), ovulatory, and mid-to-late luteal (premenstrual), in 11 healthy women. The cycle phase during which subjects began their participation was determined randomly. Plasma levels of estrogen, progesterone, luteinizing hormone (LH), testosterone, and beta-endorphin were determined at each experimental session. Participants also completed a daily diary of physical and emotional symptoms for two complete menstrual cycles before the experimental sessions. Results: The results indicated that women showed less ischemic pain sensitivity during the midfollicular compared with the ovulatory and mid-to-late luteal phases, but thermal pain responses did not vary significantly across menstrual cycle phases. Physical and emotional symptoms were minimal and did not change significantly across the menstrual cycle. Conclusions: These findings indicate greater ischemic but not thermal pain sensitivity among women after the midcycle LH surge, The practical relevance and potential mechanisms of these findings are discussed.
引用
收藏
页码:512 / 520
页数:9
相关论文
共 54 条
[1]  
BASOA MBD, 1993, BRAIN RES, V601, P241
[2]   DESENSITIZATION OF BRAIN OPIATE RECEPTOR MECHANISMS BY GONADAL-STEROID TREATMENTS THAT STIMULATE LUTEINIZING-HORMONE SECRETION [J].
BERGLUND, LA ;
DERENDORF, H ;
SIMPKINS, JW .
ENDOCRINOLOGY, 1988, 122 (06) :2718-2726
[3]  
BERGLUND LA, 1988, NEUROENDOCRINOLOGY, V48, P394, DOI 10.1159/000125040
[4]   EPIDEMIOLOGY OF PREMENSTRUAL SYMPTOMS [J].
BOYLE, CA ;
BERKOWITZ, GS ;
KELSEY, JL .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1987, 77 (03) :349-350
[5]   DIFFERENTIAL EFFECTS OF OVARIAN HORMONES ON REACTIVITY TO ELECTRIC FOOTSHOCK IN RAT [J].
DRURY, RA ;
GOLD, RM .
PHYSIOLOGY & BEHAVIOR, 1978, 20 (02) :187-191
[6]  
DUNCAN GH, 1989, P 5 WORLD C PAIN NEW, P383
[7]   OPIOID CONTROL OF THE HYPOTHALAMUS-PITUITARY-ADRENAL AXIS CYCLICALLY FAILS IN MENSTRUAL MIGRAINE [J].
FACCHINETTI, F ;
MARTIGNONI, E ;
FIORONI, L ;
SANCES, G ;
GENAZZANI, AR .
CEPHALALGIA, 1990, 10 (01) :51-56
[8]  
FACCHINETTI F, 1988, J REPROD MED, V33, P633
[9]  
Fillingim R. B., 1995, Journal of Women's Health, V4, P367, DOI [DOI 10.1089/JWH.1995.4.367, 10.1089/jwh.1995.4.367]
[10]   Gender differences in the responses to noxious stimuli [J].
Fillingim, RB ;
Maixner, W .
PAIN FORUM, 1995, 4 (04) :209-221