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COX-2 底物选择性抑制通过内源性大麻素激活降低焦虑。

Substrate-selective COX-2 inhibition decreases anxiety via endocannabinoid activation.

机构信息

A.B. Hancock Jr. Memorial Laboratory for Cancer Research, Department of Biochemistry, Vanderbilt Institute of Chemical Biology, Center in Molecular Toxicology, and Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

出版信息

Nat Neurosci. 2013 Sep;16(9):1291-8. doi: 10.1038/nn.3480. Epub 2013 Aug 4.

Abstract

Augmentation of endogenous cannabinoid (eCB) signaling represents an emerging approach to the treatment of affective disorders. Cyclooxygenase-2 (COX-2) oxygenates arachidonic acid to form prostaglandins, but also inactivates eCBs in vitro. However, the viability of COX-2 as a therapeutic target for in vivo eCB augmentation has not been explored. Using medicinal chemistry and in vivo analytical and behavioral pharmacological approaches, we found that COX-2 is important for the regulation of eCB levels in vivo. We used a pharmacological strategy involving substrate-selective inhibition of COX-2 to augment eCB signaling without affecting related non-eCB lipids or prostaglandin synthesis. Behaviorally, substrate-selective inhibition of COX-2 reduced anxiety-like behaviors in mice via increased eCB signaling. Our data suggest a key role for COX-2 in the regulation of eCB signaling and indicate that substrate-selective pharmacology represents a viable approach for eCB augmentation with broad therapeutic potential.

摘要

内源性大麻素(eCB)信号的增强代表了治疗情感障碍的一种新方法。环氧化酶-2(COX-2)将花生四烯酸氧化形成前列腺素,但也在体外使 eCB 失活。然而,COX-2 作为体内 eCB 增强的治疗靶点的可行性尚未得到探索。使用药物化学和体内分析及行为药理学方法,我们发现 COX-2 对于体内 eCB 水平的调节很重要。我们使用了一种涉及 COX-2 底物选择性抑制的药理学策略来增强 eCB 信号,而不影响相关的非 eCB 脂质或前列腺素合成。在行为上,COX-2 的底物选择性抑制通过增加 eCB 信号来减少小鼠的焦虑样行为。我们的数据表明 COX-2 在 eCB 信号调节中起着关键作用,并表明底物选择性药理学是一种具有广泛治疗潜力的可行的 eCB 增强方法。

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