Meazzi Sara, Bristi Sabiha Zarin Tasnim, Bianchini Virginia, Scarpa Paola, Giordano Alessia
Department of Veterinary Medicine and Animal Sciences, University of Milan, Via dell'Università 6, 26900 Lodi, Italy.
I-VET Laboratory, Via E. Majorana 10, 25020 Flero, Italy.
Animals (Basel). 2024 Oct 8;14(19):2886. doi: 10.3390/ani14192886.
Paraoxonase-1 (PON-1), a liver-synthesized enzyme, acts as a negative acute-phase reactant during systemic inflammation in dogs. Given the hepatic synthesis of this enzyme, the presence of liver diseases may influence PON-1, thus affecting its reliability as a biomarker for inflammatory/oxidative systemic diseases. The aim of this study is to investigate PON-1 activity variations among dogs suspected of liver injury or failure, evaluating the influence of hepatic diseases on PON-1 activity. A total of one-hundred-sixty dogs were retrospectively enrolled and categorized into three groups based on clinical presentation and laboratory results: control (C = 20), suspected liver injury (INJ = 114), and suspected liver failure (FAIL = 26). The INJ group was further divided into subgroups based on the severity of the alanine aminotransferase (ALT) increase. Both the INJ and FAIL groups were further divided based on serum macroscopic appearance. The PON-1 activity was quantified using a paraoxon-based method, which is already validated in dogs. No significant difference in PON-1 activity was observed between the C and INJ groups, despite a significant increase in the subgroups with moderate and severe elevations of ALT. The dogs with icteric serum exhibited decreased PON-1 activity, while lipemic serum was associated with an increased PON-1 activity. A significant reduction in PON-1 activity was noted in the FAIL group, compared to both C and INJ groups ( < 0.0001), regardless of serum appearance. Given the retrospective nature of this study, additional evaluations (e.g., histopathology, imaging) were not performed. The results obtained here suggest the importance of interpreting PON-1 activity cautiously in dogs with suspected liver disease.
对氧磷酶-1(PON-1)是一种肝脏合成的酶,在犬类全身炎症期间作为负急性期反应物。鉴于该酶由肝脏合成,肝脏疾病的存在可能会影响PON-1,从而影响其作为炎症/氧化全身疾病生物标志物的可靠性。本研究的目的是调查疑似肝损伤或肝衰竭犬的PON-1活性变化,评估肝脏疾病对PON-1活性的影响。总共回顾性纳入了160只犬,并根据临床表现和实验室结果分为三组:对照组(C = 20只)、疑似肝损伤组(INJ = 114只)和疑似肝衰竭组(FAIL = 26只)。INJ组根据丙氨酸氨基转移酶(ALT)升高的严重程度进一步分为亚组。INJ组和FAIL组均根据血清外观进一步划分。使用基于对氧磷的方法对PON-1活性进行定量,该方法已在犬类中得到验证。尽管ALT中度和重度升高的亚组中PON-1活性显著增加,但C组和INJ组之间未观察到PON-1活性的显著差异。血清黄疸的犬PON-1活性降低,而脂血血清与PON-1活性增加相关。与C组和INJ组相比,FAIL组的PON-1活性显著降低(<0.0001),无论血清外观如何。鉴于本研究的回顾性性质,未进行额外评估(如组织病理学、影像学检查)。此处获得的结果表明,在疑似肝脏疾病的犬中谨慎解释PON-1活性具有重要意义。