Faculty of Pharmaceutical Sciences, Sojo University, 4-22-1 Ikeda, Kumamoto 860-0082, Japan.
DDS Research Institute, Sojo University, 4-22-1 Ikeda, Kumamoto 860-0082, Japan.
Toxins (Basel). 2024 Jul 12;16(7):316. doi: 10.3390/toxins16070316.
The characteristic accumulation of circulating uremic toxins, such as indoxyl sulfate (IS), in chronic kidney disease (CKD) further exacerbates the disease progression. The gut microbiota, particularly gut bacterial-specific enzymes, represents a selective and attractive target for suppressing uremic toxin production and slowing the progression of renal failure. This study investigates the role of 4-phenylbutyrate (PB) and structurally related compounds, which are speculated to possess renoprotective properties in suppressing IS production and slowing or reversing renal failure in CKD. In vitro enzyme kinetic studies showed that 7-phenylheptanoic acid (PH), a PB homologue, suppresses the tryptophan indole lyase (TIL)-catalyzed decomposition of tryptophan to indole, the precursor of IS. A hydroxypropyl β-cyclodextrin (HPβCD) inclusion complex formulation of PH was prepared to enhance its biopharmaceutical properties and to facilitate in vivo evaluation. Prophylactic oral administration of the PH-HPβCD complex formulation reduced circulating IS and attenuated the deterioration of renal function and tubulointerstitial fibrosis in adenine-induced CKD mice. Additionally, treatment of moderately advanced adenine-induced CKD mice with the formulation ameliorated renal failure, although tissue fibrosis was not improved. These findings suggest that PH-HPβCD can slow the progression of renal failure and may have implications for preventing or managing CKD, particularly in early-stage disease.
在慢性肾脏病 (CKD) 中,循环尿毒症毒素(如硫酸吲哚酚 (IS))的特征性蓄积进一步加剧了疾病的进展。肠道微生物群,特别是肠道细菌特异性酶,代表了抑制尿毒症毒素产生和减缓肾衰竭进展的选择性和有吸引力的靶点。本研究调查了 4-苯基丁酸 (PB) 及其结构相关化合物的作用,这些化合物被推测具有抑制 IS 产生和减缓或逆转 CKD 中肾衰竭的肾保护特性。体外酶动力学研究表明,PB 同系物 7-苯基庚酸 (PH) 抑制色氨酸吲哚裂解酶 (TIL) 催化的色氨酸分解为 IS 的前体吲哚。制备了 PH 的羟丙基-β-环糊精 (HPβCD) 包合物制剂,以增强其生物制药特性并便于体内评价。预防性口服 PH-HPβCD 复合制剂可降低循环 IS 水平,并减轻腺嘌呤诱导的 CKD 小鼠肾功能恶化和肾小管间质纤维化。此外,用该制剂治疗中度进展的腺嘌呤诱导的 CKD 小鼠可改善肾衰竭,但组织纤维化未得到改善。这些发现表明 PH-HPβCD 可以减缓肾衰竭的进展,可能对预防或治疗 CKD 具有重要意义,尤其是在疾病早期。