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DOI 10.3109/01480545.2014.922095

Медицинская библиотека · Drug and chemical toxicology · 2014

Withdrawal of repeated morphine enhances histamine-induced scratching responses in mice.

Abe Kenji, Kobayashi Kanayo, Yoshino Saori, Taguchi Kyoji, Nojima Hiroshi

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

An itch is experientially well known that the scratching response of conditions such as atopic dermatitis is enhanced under psychological stress. Morphine is typical narcotic drug that induces a scratching response upon local application as an adverse drug reaction. Although long-term treatment with morphine will cause tolerance and dependence, morphine withdrawal can cause psychologically and physiologically stressful changes in humans. In this study, we evaluated the effects of morphine withdrawal on histamine-induced scratching behavior in mice. Administration of morphine with progressively increasing doses (10-50 mg/kg, i.p.) was performed for 5 consecutive days. At 3, 24, 48, and 72 hr after spontaneous withdrawal from the final morphine dose, histamine was intradermally injected into the rostral part of the back and then the number of bouts of scratching in 60 min was recorded and summed. We found that at 24 hr after morphine withdrawal there was a significant increase in histamine-induced scratching behavior. The spinal c-Fos positive cells were also significantly increased. The relative adrenal weight increased and the relative thymus weight decreased, both significantly. Moreover, the plasma corticosterone levels changed in parallel with the number of scratching bouts. These results suggest that morphine withdrawal induces a stressed state and enhances in histamine-induced scratching behavior. Increased reaction against histamine in the cervical vertebrae will participate in this stress-induced itch enhancement.

Для цитирования: Abe Kenji, Kobayashi Kanayo, Yoshino Saori, Taguchi Kyoji, Nojima Hiroshi. Withdrawal of repeated morphine enhances histamine-induced scratching responses in mice.. Drug and chemical toxicology. 2014. DOI: 10.3109/01480545.2014.922095.

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