Date published: 2025-9-17

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ROM-K Activators

ROMK Activators are a category of compounds that can indirectly influence the activity of the Renal Outer Medullary Potassium (ROMK) channel, or Kir1.1, a key protein involved in potassium transport in the nephrons of the kidney. These substances generally operate through pathways linked to electrolyte balance and cellular signaling, which in turn can impact ROMK function. Vasopressin, for instance, can stimulate aldosterone release which promotes the synthesis and trafficking of ROMK channels to the cell membrane, thereby increasing their activity. Similarly, Angiotensin II triggers the renin-angiotensin-aldosterone system (RAAS), a crucial regulator of potassium homeostasis, indirectly influencing ROMK activity. Other compounds, such as Forskolin and 8-Bromo-cyclic AMP, operate via the cAMP-protein kinase A (PKA) pathway. Forskolin elevates intracellular cAMP levels, which then activate PKA, while 8-Bromo-cyclic AMP is a cell-permeable cAMP analog that directly activates PKA. Both can impact the phosphorylation state of ROMK and thus its activity.

Polyunsaturated fatty acids, specifically Eicosapentaenoic acid (EPA) and Docosahexaenoic acid (DHA), can indirectly activate ROMK by modifying the lipid environment of the channel. This modification can affect the channel's conformation and function, leading to changes in its activity. Prostaglandin E2 (PGE2) can also indirectly influence ROMK by modulating cAMP production, leading to changes in PKA activity, and subsequently, ROMK function. Lastly, neurotransmitters such as Acetylcholine and Phenylephrine can indirectly affect ROMK through their modulation of the parasympathetic and sympathetic nervous systems, respectively, which play roles in maintaining electrolyte balance. Taken together, these ROMK Activators illustrate the complex interplay of various cellular processes and signaling pathways that can influence the activity of the ROMK channel indirectly. They underscore the importance of context and the cellular environment in shaping the impact of these compounds on ROMK function.

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