デザイナータンパク質で依存症を再構成(Rewiring Addiction With Designer Proteins)

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2025-08-27 カリフォルニア大学サンディエゴ校 (UCSD)

コカイン依存の正のフィードバックループを断ち切る新たな戦略として、UCサンディエゴ大学とNIDAの研究チームは、脳内にカスタム設計されたイオンチャネル(神経活動を制御するタンパク質)を用いる手法を開発しました。このチャネルはコカインが存在する時のみ活性化し、ラットの外側視蓋野(LHb)でドーパミン放出を抑制、コカインへの探索行動を大幅に減少させました。実験では、自然報酬(食事や運動など)による喜びは変更されなかったため、自然な快楽を維持しつつ依存だけを抑制する理想的な介入法となる可能性があります。 他の依存性物質にも応用が期待される一方で、ヒトへの応用や安全性の検証にはさらなる研究が必要です。本研究は学術誌 Nature に掲載されています。

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コカインの化学遺伝学は合成生理学によって薬物探索を鈍らせる Cocaine chemogenetics blunts drug-seeking by synthetic physiology

Juan L. Gomez,Christopher J. Magnus,Jordi Bonaventura,Oscar Solis,Fallon P. Curry,Marjorie R. Levinstein,Reece C. Budinich,Meghan L. Carlton,Emilya N. Ventriglia,Sherry Lam,Le Wang,Ingrid Schoenborn,William Dunne,Michael Michaelides &Scott M. Sternson
Nature  Published:27 August 2025
DO:Ihttps://doi.org/10.1038/s41586-025-09427-8

デザイナータンパク質で依存症を再構成(Rewiring Addiction With Designer Proteins)

Abstract

Chemical feedback is ubiquitous in physiology but is challenging to study without perturbing basal functions. One example is addictive drugs, which elicit a positive-feedback cycle of drug-seeking and ingestion by acting on the brain to increase dopamine signalling1,2,3. However, interfering with this process by altering basal dopamine also adversely affects learning, movement, attention and wakefulness4. Here, inspired by physiological control systems, we developed a highly selective synthetic physiology approach to interfere with the positive-feedback cycle of addiction by installing a cocaine-dependent opposing signalling process into this body–brain signalling loop. We used protein engineering to create cocaine-gated ion channels that are selective for cocaine over other drugs and endogenous molecules. Expression of an excitatory cocaine-gated channel in the rat lateral habenula, a brain region that is normally inhibited by cocaine, suppressed cocaine self-administration without affecting food motivation. This artificial cocaine-activated chemogenetic process reduced the cocaine-induced extracellular dopamine rise in the nucleus accumbens. Our results show that cocaine chemogenetics is a selective approach for countering drug reinforcement by clamping dopamine release in the presence of cocaine. In the future, chemogenetic receptors could be developed for additional addictive drugs or hormones and metabolites, which would facilitate efforts to probe their neural circuit mechanisms using a synthetic physiology approach. As these chemogenetic ion channels are specific for cocaine over natural rewards, they may also offer a route towards gene therapies for cocaine addiction.

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