オピオイド受容体
WordNet
- a cellular structure that is postulated to exist in order to mediate between a chemical agent that acts on nervous tissue and the physiological response
- an alkaloid narcotic drug extracted from opium; a powerful, habit-forming narcotic used to relieve pain (同)morphia
PrepTutorEJDIC
- =sense organ / 受信装置
- モルヒネ(鎮痛・麻酔剤)
UpToDate Contents
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English Journal
- Opioids and TRPV1 in the peripheral control of neuropathic pain - Defining a target site in the injured nerve.
- Labuz D1, Spahn V2, Celik MÖ3, Machelska H4.
- Neuropharmacology.Neuropharmacology.2016 Feb;101:330-40. doi: 10.1016/j.neuropharm.2015.10.003. Epub 2015 Oct 8.
- Targeting peripheral neuropathic pain at its origin may prevent the development of hypersensitivity. Recently we showed this can be mediated by opioid receptors at the injured nerve trunk. Here, we searched for the most relevant peripheral site to block transient receptor potential vanilloid 1 (TRPV
- PMID 26453963
- Activation of serotonin 5-HT2C receptor suppresses behavioral sensitization and naloxone-precipitated withdrawal symptoms in morphine-dependent mice.
- Zhang G1, Wu X2, Zhang YM3, Liu H2, Jiang Q2, Pang G2, Tao X4, Dong L2, Stackman RW Jr5.
- Neuropharmacology.Neuropharmacology.2016 Feb;101:246-54. doi: 10.1016/j.neuropharm.2015.09.031. Epub 2015 Dec 3.
- Opioid abuse and dependence have evolved into an international epidemic as a significant clinical and societal problem with devastating consequences. Repeated exposure to the opioid, for example morphine, can induce profound, long-lasting behavioral sensitization and physical dependence, which are t
- PMID 26432939
- Opiorphin causes a panicolytic-like effect in rat panic models mediated by μ-opioid receptors in the dorsal periaqueductal gray.
- Maraschin JC1, Rangel MP2, Bonfim AJ2, Kitayama M2, Graeff FG3, Zangrossi H Jr4, Audi EA5.
- Neuropharmacology.Neuropharmacology.2016 Feb;101:264-70. doi: 10.1016/j.neuropharm.2015.09.008. Epub 2015 Sep 10.
- Reported evidence indicates that endogenous opioid peptides regulate the expression of escape behavior in rats, a panic-related defensive response, through μ-opioid receptors (MORs) in the dorsal periaqueductal gray (dPAG). These peptides are rapidly catabolized by degrading enzymes, including neut
- PMID 26363194
Japanese Journal
- Attenuation of morphine antinociceptive tolerance by cannabinoid CB1 and CB2 receptor antagonists
- 神経障害性疼痛下における薬物トランスポーターの発現とモルヒネの鎮痛効果の変動
- Potential Involvement of μ-Opioid Receptor Dysregulation on the Reduced Antinociception of Morphine in the Inflammatory Pain State in Mice
Related Links
- Morphine has been widely accepted as the opioid agonist that sustains signaling because it does not cause receptor desensitization or internalization. This notion has led to the hypothesis that long-term morphine treatment initiates ...
- 1. Adv Neuroimmunol. 1994;4(2):69-82. Morphine receptors in immunocytes and neurons. Makman MH. Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York 10461. Receptor interactions of morphine are ...
★リンクテーブル★
[★]
- 英
- opioid receptor
- 同
- モルヒネ受容体 morphine receptor
- 関
- オピオイドペプチド、オピオイド
- オピオイド受容体はμ受容体、κ受容体、δ受容体がある。
- モルヒネ、フェンタニルはμ受容体刺激薬
- 呼吸抑制はμ2受容体を介したものである。
オピオイドとオピオイド受容体 (GOO.552)
オピオイド受容体の生理作用(周術期管理学 091211 III)
受容体
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μ
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δ
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κ
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μ1
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μ2
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作用
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鎮痛
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鎮痛
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鎮痛
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鎮痛
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悪心・嘔吐
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鎮静
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鎮静
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身体依存
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多幸感
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呼吸抑制
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身体違和感
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精神依存
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掻痒感
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身体依存
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気分不快
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呼吸抑制
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縮瞳
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精神依存
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興奮
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尿閉
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消化器運動抑制
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幻覚
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鎮咳
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鎮咳
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呼吸抑制
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縮瞳
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利尿
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オピオイド受容体と非麻薬性鎮痛薬について
身体依存性
- 痛みがある人には精神的依存はきたさない(痛みの有無によらず退薬現象はある)
[★]
- 英
- morphine receptor
- 同
- オピオイド受容体、アヘン類受容体