Johnson Bency Elsa, Haritha C V, Mathesh Karikalan, Vamadevan Beena, Sharma Anshuk, Aneesha V A, Jadhav Sunil E, Parida Subhashree, Singh Thakur Uttam, Lingaraju Madhu Cholenahalli
Division of Pharmacology and Toxicology, ICAR-Indian Veterinary Research Institute, Izatnagar, 243 122, India.
Centre for Wildlife Conservation, Management and Disease Surveillance, ICAR-Indian Veterinary Research Institute, Izatnagar, 243 122, India.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Jan 17. doi: 10.1007/s00210-024-03728-x.
Betulinic acid (BA) has been shown to exhibit various pharmacological activities and it has shown the protective effect on acute renal failure (ARF) and chronic renal failure (CRF); however, no reports are available on its effect on ARF-CRF transition. Therefore, we aimed to investigate the effects of BA on ARF-CRF transition. A single dose of 250 mg/kg body weight (BW) intraperitoneal injection of folic acid was given in mice for inducing ARF-CRF transition (injury group; I) on day 1. Further, excess of these mice received BA at 30 mg/kg BW dose for 3 days (on days 1, 2, 3) in one group (IT3) and for 7 days (on days 1, 2, 3, 7, 14, 21, 28) in another group (IT7). All mice were sacrificed on day 28. Mice in injury group (I) showed elevated serum creatinine along with oxidative stress markers like urine nitrite, tissue lipid peroxidation, nitrotyrosine and fibrotic markers such as tissue α-smooth muscle actin and matrix metalloproteinase-2 activity. They had attenuated levels of urine creatinine and tissue reparative cytokines viz. interleukin-4 and interleukin-13. Excess of fibroblasts and extracellular matrix in the interstitia and periglomerular area in microscopy further support these findings. Seven days of BA treatment regimen (IT7) significantly improved serum and urine parameters accompanied by reduced oxidative stress, improved reparative cytokines and lesser maladaptive matrix deposition. The above findings reveal that weekly BA treatment regimen has potential to prevent development of CRF after ARF.
桦木酸(BA)已被证明具有多种药理活性,并且对急性肾衰竭(ARF)和慢性肾衰竭(CRF)均显示出保护作用;然而,尚无关于其对ARF向CRF转变影响的报道。因此,我们旨在研究BA对ARF向CRF转变的影响。在第1天,给小鼠腹腔注射单剂量250 mg/kg体重的叶酸以诱导ARF向CRF转变(损伤组;I)。此外,这些小鼠中的一部分在一组(IT3)中以30 mg/kg体重的剂量接受BA治疗3天(第1、2、3天),在另一组(IT7)中接受7天(第1、2、3、7、14、21、28天)。所有小鼠在第28天处死。损伤组(I)的小鼠血清肌酐升高,同时伴有氧化应激标志物如尿亚硝酸盐、组织脂质过氧化、硝基酪氨酸以及纤维化标志物如组织α平滑肌肌动蛋白和基质金属蛋白酶-2活性升高。它们的尿肌酐水平和组织修复性细胞因子即白细胞介素-4和白细胞介素-13水平降低。显微镜下间质和肾小球周围区域的成纤维细胞和细胞外基质增多进一步支持了这些发现。7天的BA治疗方案(IT7)显著改善了血清和尿液参数,同时氧化应激减轻、修复性细胞因子改善且适应性不良的基质沉积减少。上述发现表明,每周一次的BA治疗方案有可能预防ARF后CRF的发生。