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. 2023 Jun;39(5):317-323.
doi: 10.1089/jop.2022.0180. Epub 2023 Apr 25.

Carbonic Anhydrase Inhibitor Modulation of Intraocular Pressure Is Independent of Soluble Adenylyl Cyclase

Affiliations

Carbonic Anhydrase Inhibitor Modulation of Intraocular Pressure Is Independent of Soluble Adenylyl Cyclase

Shakarr V Wiggins et al. J Ocul Pharmacol Ther. 2023 Jun.

Abstract

Purpose: We investigated whether a clinically used carbonic anhydrase inhibitor (CAIs) can modulate intraocular pressure (IOP) through soluble adenylyl cyclase (sAC) signaling. Methods: IOP was measured 1 h after topical treatment with brinzolamide, a topically applied and clinically used CAIs, using direct cannulation of the anterior chamber in sAC knockout (KO) mice or C57BL/6J mice in the presence or absence of the sAC inhibitor (TDI-10229). Results: Mice treated with the sAC inhibitor TDI-10229 had elevated IOP. CAIs treatment significantly decreased increased intraocular pressure (IOP) in wild-type, sAC KO mice, as well as TDI-10229-treated mice. Conclusions: Inhibiting carbonic anhydrase reduces IOP independently from sAC in mice. Our studies suggest that the signaling cascade by which brinzolamide regulates IOP does not involve sAC.

Keywords: IOP; cAMP; carbonic anhydrase; intraocular pressure; pharmacological inhibitors; soluble adenylyl cyclase.

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Conflict of interest statement

L.R.L. and J.B. are cofounders of Sacyl Pharmaceuticals, Inc., established to develop sAC inhibitors into on-demand contraceptives. All other authors declare that they have no conflicts of interest with the contents of this article.

Figures

FIG. 1.
FIG. 1.
The concentration of cAMP in sAC-overexpressing 4-4 cells. Cellular accumulation of cAMP was measured in cells pretreated with inhibitors for 10 min followed by treatment with 500 μM IBMX and 30 μM DP (IBMX+DP) for 10 min, mean ± SEM (n = 3). DP, dipyridamole; cAMP, cyclic 3′, 5′ adenosine monophosphate; sAC, soluble adenylyl cyclase; SEM, standard error of the mean.
FIG. 2.
FIG. 2.
The concentration-response of TDI-10229, a potent and selective sAC inhibitor, acetazolamide (green) and brinzolamide (orange) on purified recombinant human sAC protein in the presence of 1 mM ATP, 2 mM Ca2+, 4 mM Mg2+, and 40 mM HCO3, normalized to the respective DMSO-treated control; mean ± SEM (n = 3). ATP, adenosine triphosphate; DMSO, dimethylsulfoxide.
FIG. 3.
FIG. 3.
Brinzolamide decreases IOP in both WT and sAC KO mice. IOP was measured in WT (sAC+/+, C57BL/6J) or KO (sAC−/−) mice after 1 h treatment with topical brinzolamide (1 drop (15 μL) of 10 mg/mL). The line indicates mean. n = 101 sAC+/+, n = 26 sAC+/+ with brinzolamide, n = 27 sAC−/−, n = 12 sAC−/− with brinzolamide. *P < 0.05, **P < 0.01. IOP, increased intraocular pressure; KO, knockout; WT, wild-type.
FIG. 4.
FIG. 4.
Administration of brinzolamide decreases IOP in both vehicle and TDI-10229-treated wild-type mice (sAC+/+, C57BL/6J). IOP was measured in mice IP injected with vehicle (DMSO) or TDI-10229 (20 mg/kg) and treated topically with vehicle or brinzolamide [1 drop (15 μL) of 10 mg/mL]. The line indicates mean. n = 52 sAC+/+ with DMSO, n = 30 sAC+/+ with DMSO + brinzolamide, n = 29 TDI-10229 sAC+/+, n = 15 sAC+/+ with TDI-10229 + brinzolamide. **P < 0.01, ***P < 0.001, and ****P < 0.0001. IP, intraperitoneally.

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