Neonatal maternal separation alters stress-induced responses to viscerosomatic nociceptive stimuli in rat

被引:357
作者
Coutinho, SV
Plotsky, PM
Sablad, M
Miller, JC
Zhou, H
Bayati, AI
McRoberts, JA
Mayer, EA
机构
[1] Univ Calif Los Angeles, Sch Med, Brain Res Inst, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Brain Res Inst, Dept Physiol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Sch Med, Brain Res Inst, Dept Biobehav Sci, Los Angeles, CA 90095 USA
[4] Emory Univ, Sch Med, Stress Neurobiol Lab, Atlanta, GA 30322 USA
[5] AstraZeneca R&D, S-543183 Molndal, Sweden
[6] Univ Calif Los Angeles, Sch Med, CURE, Neuroenter Dis Program, Los Angeles, CA 90095 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2002年 / 282卷 / 02期
关键词
irritable bowel syndrome; stress; analgesia; naloxone;
D O I
10.1152/ajpgi.00240.2001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
This study investigated the combined effect of neonatal maternal separation and acute psychological stress on pain responses in adult rats. Long-Evans dams and their male pups were reared under two conditions: 1) 180 min daily maternal separation (MS180) on postnatal days 2-14 or 2) no handling or separation (NH). At 2 mo of age, visceromotor responses to graded intensities of phasic colorectal distension (10-80 mmHg) at baseline as well as following acute 60 min water avoidance stress (WA) were significantly higher in MS180 rats. Both groups showed similar stress-induced visceral hyperalgesia in the presence of naloxone (20 mg/kg ip). MS180 rats had smaller stress-induced cutaneous analgesia in the tail-flick test compared with NH rats, with a residual naloxone-resistant component. MS180 rats showed an enhanced fecal pellet output following WA or exposure to a novel environment. These data suggest that early life events predispose adult Long-Evans rats to develop visceral hyperalgesia, reduced somatic analgesia, and increased colonic motility in response to an acute psychological stressor, mimicking the cardinal features of irritable bowel syndrome.
引用
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页码:G307 / G316
页数:10
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