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Although human mutations in OAT1 have not been described, these pathways could also be inhibited by medication and endogenous toxins, thereby inflicting diuretic resistance ( 31 ). Nonsteroidal anti-inflammatory medicine (NSAIDs) inhibit diuretic secretion and alter diuretic responsiveness, and due to their frequent use, are an essential explanation for heart failure exacerbations ( 34 ). But different lessons of medication, together with antihypertensives, antibiotics, and antivirals, may also interact with these transporters and trigger resistance ( 35 ). Endogenous metabolites additionally compete for diuretic secretion, including indoxyl sulfate, carboxy-methyl-propyl-furanpropionate, p-cresol sulfate, and kynurenate, which accumulate in CKD ( 36 ). In all of these conditions, the natriuretic dose-response curve is shifted to the best ( Figure 3A ).