IMPACT OF MORPHINE DEPENDENCE ON NOS POSITIVE NEURONS IN MICE HIPPOCAMPUS
Yang Chunrong
Abstract
Yang Chunrong
Abstract
Objective: To study the impact of morphine dependence on the activity of NOS in subareas of mice hippocampus.Methods: Mice were given (sc) gradually increasing doses of morphine to form morphine dependent model. NADPH-diaphorase with a histochemical method was used to study the distribution areas of NOS positive neurons in CA1, dentate gyrus and CA3 of hippocampus of morphine dependent group, naloxone-precipitated withdrawal group in morphine dependent mice and control group. Results: Compared with control group , the number of positive cells decreased obviously in CA1 and dentate gyrus of both groups in morphine dependent mice, especially the later. Conclusion: The activity of NOS in CA1 and dentate gyrus of morphine dependent and naloxone-precipitated withdrawal groups has decreased, especially the later, which suggests that the synthesis of NO has decreased. Those changes may be some of the reasons causing learning and memory deficits.
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Objective: To study the impact of morphine dependence on the activity of NOS in subareas of mice hippocampus.Methods: Mice were given (sc) gradually increasing doses of morphine to form morphine dependent model. NADPH-diaphorase with a histochemical method was used to study the distribution areas of NOS positive neurons in CA1, dentate gyrus and CA3 of hippocampus of morphine dependent group, naloxone-precipitated withdrawal group in morphine dependent mice and control group. Results: Compared with control group , the number of positive cells decreased obviously in CA1 and dentate gyrus of both groups in morphine dependent mice, especially the later. Conclusion: The activity of NOS in CA1 and dentate gyrus of morphine dependent and naloxone-precipitated withdrawal groups has decreased, especially the later, which suggests that the synthesis of NO has decreased. Those changes may be some of the reasons causing learning and memory deficits.
Key concepts: Dentate gyrus, Morphine, Hippocampus, (+)-Naloxone, Internal medicine, Psychology, Endocrinology, Anesthesia