Hyperalgesic response to noxious stimulation in genetically polydipsic mice

Hideki Kamikawa, Toshihiko Katafuchi, Masako Hosoi, Tsuneyuki Yamamoto, Tetsuro Hori

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


Inbred mice, STR/N, are known to exhibit extreme polydipsia and polyuria but no abnormality in the response to exogenous vasopressin (AVP) and renal functions. Our previous studies have revealed that the brain opioid system is involved in the polydipsia of these mice. We here report that the STR/N mice show a decrease in the nociceptive threshold and a low, anti-nociceptive sensitivity to opioid receptors agonists. The paw-withdrawal latency (PWL) on a hot-plate in the STR/N mice was significantly shorter than that in their controls (BALB/c and C3H mice). This hyperalgesia was not affected by water restriction. Subcutaneous (s.c.) injections of morphine (5 mg/kg) and a κ-opioid receptor agonist, U50,488H (16 mg/kg) had no effect on the PWL in the STR/N mice, whereas the control mice prolonged PWL after administration of the opioids. However, the STR/N mice gained the ability to show morphine analgesia after up-regulation of the opioid system by repeated administration of naltrexone (s.c., 5 mg/kg) for 3 consecutive days. The results suggest that the anti-nociceptive function of the opioid system is down-regulated in STR/N mice as is observed in chronic morphine-treated animals. Copyright (C) 1999 Elsevier Science B.V.

Original languageEnglish
Pages (from-to)171-176
Number of pages6
JournalBrain Research
Issue number2
Publication statusPublished - Nov 6 1999

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology


Dive into the research topics of 'Hyperalgesic response to noxious stimulation in genetically polydipsic mice'. Together they form a unique fingerprint.

Cite this