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

被引:358
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
收藏
页码:G307 / G316
页数:10
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