Yenice Guler, Ozkanlar Seckin, Bolat Ismail, Yildirim Serkan
Faculty of Veterinary Medicine, Department of Animal Nutrition and Nutritional Disorders, Ataturk University, Erzurum, Turkey.
Faculty of Veterinary Medicine, Department of Biochemistry, Ataturk University, Erzurum, Turkey.
Basic Clin Pharmacol Toxicol. 2025 Jun;136(6):e70052. doi: 10.1111/bcpt.70052.
Acute pancreatitis (AP) is a serious pancreatic inflammatory disease that results in pancreatic enzyme activation and autodegradation. Betulinic acid (BA), a pentacyclic triterpene of natural origin that was isolated from several plants, has anti-inflammatory, immunomodulatory and antioxidant effects that can help with AP. With this study, we aimed to investigate the potential positive effects of BA on l-arginine-induced AP. A total of 24 male rats were divided into four groups (control, BA, AP and BA + AP). Animals in the BA group were given BA 50 mg/kg/day for 7 days. AP was induced by administering two doses of 250-mg/100-g l-arginine to animals in the AP group. The animals in the BA + AP group were administered 50-mg/kg/day BA (gavage) for 7 days and two doses of 250-mg/100-g l-arginine on the seventh day. BA pretreatment inhibited the increased lipase activity caused by AP and showed protective activity against oxidative damage to pancreatic tissue. It decreased the severity of inflammation by suppressing the release of pro-inflammatory cytokines while increasing the level of the anti-inflammatory cytokine IL-10. It showed a protective effect on pancreatic tissue by inhibiting tumour necrosis factor (TNF-α) and Bax expression. The findings of the study show that BA exhibits multifaceted protective activity in experimental AP induced with l-arginine.
急性胰腺炎(AP)是一种严重的胰腺炎症性疾病,可导致胰腺酶激活和自身消化。桦木酸(BA)是一种从多种植物中分离出来的天然五环三萜,具有抗炎、免疫调节和抗氧化作用,有助于治疗AP。在本研究中,我们旨在探讨BA对左旋精氨酸诱导的AP的潜在积极作用。总共24只雄性大鼠被分为四组(对照组、BA组、AP组和BA + AP组)。BA组动物每天给予50 mg/kg的BA,持续7天。通过给AP组动物注射两剂250 mg/100 g的左旋精氨酸来诱导AP。BA + AP组动物每天经口灌胃给予50 mg/kg的BA,持续7天,并在第7天注射两剂250 mg/100 g的左旋精氨酸。BA预处理可抑制AP引起的脂肪酶活性增加,并对胰腺组织的氧化损伤具有保护活性。它通过抑制促炎细胞因子的释放,同时增加抗炎细胞因子IL-10的水平,降低了炎症的严重程度。它通过抑制肿瘤坏死因子(TNF-α)和Bax的表达,对胰腺组织表现出保护作用。研究结果表明,BA在左旋精氨酸诱导的实验性AP中表现出多方面的保护活性。