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昼夜节律通过糖皮质激素和交感神经系统的双重途径调节眼压节律。

Circadian Regulation of IOP Rhythm by Dual Pathways of Glucocorticoids and the Sympathetic Nervous System.

机构信息

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出版信息

Invest Ophthalmol Vis Sci. 2020 Mar 9;61(3):26. doi: 10.1167/iovs.61.3.26.

Abstract

PURPOSE

Elevated IOP can cause the development of glaucoma. The circadian rhythm of IOP depends on the dynamics of the aqueous humor and is synchronized with the circadian rhythm pacemaker, that is, the suprachiasmatic nucleus. The suprachiasmatic nucleus resets peripheral clocks via sympathetic nerves or adrenal glucocorticoids. However, the detailed mechanisms underlying IOP rhythmicity remain unclear. The purpose of this study was to verify this regulatory pathway.

METHODS

Adrenalectomy and/or superior cervical ganglionectomy were performed in C57BL/6J mice. Their IOP rhythms were measured under light/dark cycle and constant dark conditions. Ocular administration of corticosterone or norepinephrine was also performed. Localization of adrenergic receptors, glucocorticoid receptors, and clock proteins Bmal1 and Per1 were analyzed using immunohistochemistry. Period2::luciferase rhythms in the cultured iris/ciliary bodies of adrenalectomized and/or superior cervical ganglionectomized mice were monitored to evaluate the effect of the procedures on the local clock. The IOP rhythm of retina and ciliary epithelium-specific Bmal1 knockout mice were measured to determine the significance of the local clock.

RESULTS

Adrenalectomy and superior cervical ganglionectomy disrupted IOP rhythms and the circadian clock in the iris/ciliary body cultures. Instillation of corticosterone and norepinephrine restored the IOP rhythm. β2-Adrenergic receptors, glucocorticoid receptors, and clock proteins were strongly expressed within the nonpigmented epithelia of the ciliary body. However, tissue-specific Bmal1 knock-out mice maintained their IOP rhythm.

CONCLUSIONS

These findings suggest direct driving of the IOP rhythm by the suprachiasmatic nucleus, via the dual corticosterone and norepinephrine pathway, but not the ciliary clock, which may be useful for chronotherapy of glaucoma.

摘要

目的

眼内压升高可导致青光眼的发生。眼压的昼夜节律依赖于房水的动力学,并且与昼夜节律起搏器同步,即视交叉上核。视交叉上核通过交感神经或肾上腺糖皮质激素重置外周时钟。然而,眼压节律性的详细机制尚不清楚。本研究旨在验证该调节途径。

方法

在 C57BL/6J 小鼠中进行肾上腺切除术和/或颈上交感神经节切除术。在光/暗循环和持续黑暗条件下测量其眼压节律。还进行了皮质酮或去甲肾上腺素的眼部给药。使用免疫组织化学分析肾上腺素能受体、糖皮质激素受体以及时钟蛋白 Bmal1 和 Per1 的定位。监测去肾上腺和/或颈上交感神经节切除小鼠培养的虹膜/睫状体中 Period2::luciferase 的节律,以评估这些操作对局部时钟的影响。测量视网膜和睫状上皮特异性 Bmal1 敲除小鼠的眼压节律,以确定局部时钟的重要性。

结果

肾上腺切除术和颈上交感神经节切除术破坏了虹膜/睫状体培养物中的眼压节律和昼夜节律时钟。皮质酮和去甲肾上腺素的滴注恢复了眼压节律。β2-肾上腺素能受体、糖皮质激素受体和时钟蛋白在睫状体的非色素上皮中强烈表达。然而,组织特异性 Bmal1 敲除小鼠保持其眼压节律。

结论

这些发现表明,视交叉上核通过双重皮质酮和去甲肾上腺素途径直接驱动眼压节律,而不是睫状时钟,这可能对青光眼的时间治疗有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c2/7401506/57318531c624/iovs-61-3-26-f001.jpg

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