GI Endoscopy

Mechanism of action of PCABs (Potasium-Competitive Acid Blockers)

Background:

Conventional proton pump inhibitors (PPIs) are the main first-line therapy to treat acid-related disorders (1). However, they have a number of limitations including slow onset of action, influence by cytochrome P450 polymorphisms, unsatisfactory effects at night, and instability in acidic conditions (1). Potassium-competitive acid blockers (P-CABs) induce a rapid, long-lasting, and reversible inhibition of the gastric hydrogen potassium ATPase, the proton pump of the stomach (1). These agents have a faster onset of action than PPIs, and they have a more sustained action in inhibiting acid secretion. Thus, they represent a new option to treat acid-related disorders. Herby we summarize the mechanism of action of PCABs.

Key Aspects:

- Proton pumps (H1, K1-ATPase) are stored in tubulovesicles in the cytoplasm of parietal cells and are kept in an inactive state. 

- Activation of proton pumps occurs after their insertion into the extracytoplasmic secretory canalicular membrane at the luminal border. 

- PPIs bind to cysteines located on the exposed site of active proton pumps, blocking exchange of hydrogen and potassium ions (yellow arrow).

- However, PPIs require an acidic environment for activation. 

- PCABs bind reversibly to K+ ions and block the H+, K+ ATPase enzyme, thus preventing acid production. PCABs block the access of potassium ions to the potassium-binding site of the pump.

- Importantly, PCAB (Potassium Competitive Acid Blocker) accumulation and binding are NOT pH-dependent, allowing PCABs to bind to both inactive and active proton pumps (red arrow).

Ref:

1.    Oshima T, Miwa H. Potent Potassium-competitive Acid Blockers: A New Era for the Treatment of Acid-related Diseases. J Neurogastroenterol Motil. 2018 Jul 30;24(3):334-344. 

2.    Laine L, et al. Pharmacodynamics and Pharmacokinetics of the Potassium-Competitive Acid Blocker Vonoprazan and the Proton Pump Inhibitor Lansoprazole in US Subjects. Am J Gastroenterol;2022:117:1158-1161