Mercantepe Tolga, Kalkan Yıldıray, Tumkaya Levent, Sehitoglu İbrahim, Mercantepe Filiz, Yıldırmıs Sermet
Departments of Histology and Embryology, Faculty of Medicine, Recep Tayyip Erdogan University, Rize, Turkey.
Department of Pathology, Faculty of Medicine, Recep Tayyip Erdogan University, Rize, Turkey.
Adv Clin Exp Med. 2018 Jun;27(6):715-720. doi: 10.17219/acem/68967.
Methotrexate (MTX), a folate antagonist, is commonly used in the treatment of many different types of cancer and inflammatory diseases, including pancreatic cancer, although its side effects on the pancreas have not yet been researched. The mechanism of MTX-induced toxicity is not well known, and it has been reported in high-dose toxicity studies that the pancreas is sensitive to toxic effects.
The aim of our study was to determine whether adalimumab (ADA) has a preventive effect on MTX-induced pancreas toxicity in rats.
The rats were equally and randomly divided into 3 groups (Group 1 comprised the healthy controls, Group 2 was the MTX group, and Group 3 was the MTX + ADA group). The rats in Groups 2 and 3 received an intraperitoneal (ip.) single-dose injection of MTX (20 mg/kg). A single dose of 5 mg/kg ADA (REMICADE®) was administered ip. to Group 3. All the rats were sacrificed under anesthesia 5 days after receiving the MTX injection.
Significantly higher mean edema, necrotic cell, and inflammatory scores were recorded in Groups 2 and 3 compared to those recorded in Group 1. Significantly decreased edema, number of necrotic cells, and inflammatory scores were noted in Group 3 than in Group 2. A decrease in islets of Langerhans cell insulin and somatostatin-positive interneurons was demonstrated after the administration of MTX. An increase in insulin and somatostatin-positive cells in islets of Langerhans, as well as a remodeling of the structure of the pancreas, was shown following treatment with ADA.
Adalimumab was demonstrated to have a protective effect against MTX-induced pancreatic injury in this study.
甲氨蝶呤(MTX)是一种叶酸拮抗剂,常用于治疗多种不同类型的癌症和炎症性疾病,包括胰腺癌,尽管其对胰腺的副作用尚未得到研究。MTX诱导毒性的机制尚不清楚,并且在高剂量毒性研究中已报道胰腺对毒性作用敏感。
我们研究的目的是确定阿达木单抗(ADA)对大鼠MTX诱导的胰腺毒性是否具有预防作用。
将大鼠平均随机分为3组(第1组为健康对照组,第2组为MTX组,第3组为MTX + ADA组)。第2组和第3组的大鼠接受腹腔内(ip.)单剂量注射MTX(20 mg/kg)。向第3组腹腔内注射单剂量5 mg/kg ADA(修美乐®)。在接受MTX注射5天后,所有大鼠在麻醉下处死。
与第1组相比,第2组和第3组的平均水肿、坏死细胞和炎症评分显著更高。第3组的水肿、坏死细胞数量和炎症评分比第2组显著降低。MTX给药后,胰岛细胞胰岛素和生长抑素阳性中间神经元减少。ADA治疗后,胰岛中胰岛素和生长抑素阳性细胞增加,以及胰腺结构重塑。
在本研究中,阿达木单抗被证明对MTX诱导的胰腺损伤具有保护作用。