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Investigative Ophthalmology & Visual Science· 2026Q1

Adrenergic Pathways Mediate Circadian IOP Rhythm in Rats

Alexandra Zamitalo-Pomares, Christopher L. Passaglia

Short summary

Topical application of adrenergic antagonists (timolol, bunazosin, yohimbine, brimonidine) during subjective night (SN) in rats significantly reduced intraocular pressure (IOP) by over 90%, while agonists (phenylephrine, isoproterenol) during subjective day (SD) elevated IOP by 60-140%.

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Key points

  • Rats exhibit a persistent circadian rhythm of intraocular pressure (IOP) even in constant darkness.
  • Topical adrenergic antagonists (timolol, bunazosin, yohimbine, brimonidine) applied during subjective night significantly reduced IOP (>90%).
  • Topical adrenergic agonists (phenylephrine, isoproterenol) applied during subjective day significantly elevated IOP (60-140%).
  • Adrenergic receptor inactivation did not alter the period or phase of the IOP rhythm, but bunazosin temporarily abolished it.
  • All adrenergic pathways are required to raise IOP during subjective night; beta- and alpha1-receptor activation is sufficient to raise IOP during subjective day.

AI-generated from the title and abstract; the full text is not read.

Abstract

Purpose: This study sought to define adrenergic receptor mechanisms underlying circadian intraocular pressure (IOP) regulation in rats. Methods: IOP was monitored continuously via wireless telemetry in adult Brown-Norway rats entrained to the ambient light/dark (LD) cycle and then maintained in constant darkness (DD). Agonists and antagonists of β- (isoproterenol and timolol), α1- (phenylephrine and bunazosin), and α2- (brimonidine and yohimbine) receptors were applied topically to the cornea during subjective day (SD) and subjective night (SN) in DD. Drug effects were quantified by short-term changes in mean IOP and long-term changes in IOP rhythmicity. Results: Animals exhibited a pronounced IOP rhythm in LD that persisted in DD. IOP was significantly reduced after SN instillation of timolol (DSN% = -110% ± 24%), bunazosin (DSN% = -107% ± 13%), yohimbine (DSN% = -106% ± 12%), and brimonidine (DSN% = -94% ± 18%) and was unchanged after SD instillation. Conversely, IOP was significantly elevated after SD instillation of phenylephrine (DSD% = 143% ± 62%) and isoproterenol (DSD% = 62% ± 19%) and was unchanged after SN instillation. None of the drugs altered IOP rhythm period or phase, but bunazosin abolished the rhythm for several days. Conclusions: Multiple adrenergic receptor pathways participate in the circadian regulation of rat IOP. All are necessary to raise IOP during SN since inactivation of any individual pathway drops IOP fully back to daytime levels. β- and α1-receptor activation is also singularly sufficient to raise IOP during SD to nighttime levels, whereas α2-receptors play a more complex role in IOP regulation.

The authors' abstract, as published at the source. Investigative Ophthalmology & Visual Science, 2026 · DOI ↗

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Field: Endocrine and Autonomic Systems

Endocrine and Autonomic SystemsNeuroscience