Van Mulders Laurens, Vanhaecke Lynn, Locquet Laurent, Skotarek Marcin, Spruyt Jonas, Quievy Alicia, Vercammen Francis, Smets Pascale, Daminet Sylvie
Faculty of Veterinary Medicine, Department of Small Animals and Laboratory of Integrative Metabolomics, B-9820 Merelbeke, Belgium,
Centre for Research and Conservation: Royal Zoological Society of Antwerp, 2018 Antwerpen, Belgium.
J Zoo Wildl Med. 2025 Jun;56(2):258-271. doi: 10.1638/2024-0094.
Lions () share an intrinsic susceptibility to chronic kidney disease (CKD) with other species of the Felidae. Interestingly, specific gut-derived uremic toxins-indoxyl sulfate, -cresyl sulfate, and trimethylamine -oxide (TMAO)-find their origin in amino acids highly abundant in the strict carnivorous feline diet. These toxins are well-recognized mediators of renal tubular inflammation and are associated with disease progression in cats Therefore, a potential causal involvement of gut-derived uremic toxicity in the pathophysiology of CKD can be hypothesized in Felidae. However, it remains undetermined whether increased accumulation of these toxins is interconnected with renal dysfunction in other Felidae. Therefore, the present study aimed at uncovering shifts in gut-derived uremic toxins and related pathways associated with renal dysfunction in lions by using a targeted metabolomic approach, comparing serum and urine profiles of lions diagnosed with CKD ( = 6) and healthy controls ( = 9). Our results show that selected gut-derived uremic toxins (indoxyl sulfate, = 0.017; TMAO, = 0.021; and -cresyl sulfate, = 0.020) were increased in lions with renal dysfunction. Our study further underscores the role of a decreasing glomerular filtration rate and tubular dysfunction in toxin accumulation. Especially, indoxyl sulfate showed increased serum-to-urine ratios indicative of renal retention. However, TMAO demonstrated a different pattern, suggesting alternative mechanisms for its elevation in CKD, such as augmented intestinal microbial formation or adsorption of its precursor trimethylamine. Moreover, clear associations between circulating uremic toxin concentrations and renal proteinuria, a marker of tubular dysfunction or damage, were observed, further substantiating the potential underlying role of gut-derived uremic toxicity in the pathophysiology of CKD in lions. Collectively, our findings form a first rationale to implement dietary modifications aimed at mitigating toxin burden in the management of Felidae diagnosed with CKD.
狮子与其他猫科动物一样,天生易患慢性肾病(CKD)。有趣的是,特定的肠道源性尿毒症毒素——硫酸吲哚酚、硫酸对甲酚和氧化三甲胺(TMAO)——源于严格食肉的猫科动物饮食中高度丰富的氨基酸。这些毒素是肾小管炎症的公认介质,与猫的疾病进展有关。因此,可以假设肠道源性尿毒症毒性在猫科动物慢性肾病的病理生理学中可能存在因果关系。然而,这些毒素的积累增加是否与其他猫科动物的肾功能障碍相互关联仍未确定。因此,本研究旨在通过靶向代谢组学方法,比较被诊断为慢性肾病的狮子(n = 6)和健康对照(n = 9)的血清和尿液谱,揭示狮子肠道源性尿毒症毒素的变化以及与肾功能障碍相关的途径。我们的结果表明,选定的肠道源性尿毒症毒素(硫酸吲哚酚,P = 0.017;TMAO,P = 0.021;和硫酸对甲酚,P = 0.020)在肾功能障碍的狮子中有所增加。我们的研究进一步强调了肾小球滤过率降低和肾小管功能障碍在毒素积累中的作用。特别是,硫酸吲哚酚的血清与尿液比值增加,表明肾脏潴留。然而,TMAO表现出不同的模式,表明其在慢性肾病中升高的替代机制,如肠道微生物形成增加或其前体三甲胺的吸附。此外,观察到循环尿毒症毒素浓度与肾蛋白尿(肾小管功能障碍或损伤的标志物)之间存在明显关联,进一步证实了肠道源性尿毒症毒性在狮子慢性肾病病理生理学中的潜在作用。总体而言,我们的研究结果为实施饮食调整以减轻被诊断为慢性肾病的猫科动物的毒素负担提供了首个理论依据。