Qaen School of Nursing and Midwifery, Birjand University of Medical Sciences, Birjand, Iran.
Department of Clinical Biochemistry, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran.
Turk J Med Sci. 2023 Feb;53(1):10-18. doi: 10.55730/1300-0144.5553. Epub 2023 Feb 22.
Diabetes is a multifactorial and growing disease, one of the severe complications of which is diabetic nephropathy (DN), which is the most common cause of chronic renal failure. FERM domain containing 3 (FRMD3) is responsible for maintaining the shape and integrity of nephron cells, and bone morphogenetic protein 7 (BMP7) helps maintain function and reduce kidney damage. This study aimed to evaluate the effect of crocin and losartan on biochemical parameters and the expression of FRMD3 and BMP7 genes in streptozotocin (STZ)-induced diabetic rats.
Forty male Wistar rats were randomly divided into five experimental groups as healthy, diabetic control (D), crocin, losartan, and diabetic rats treated with losartan-crocin (n = 8). A single dose of STZ (50 mg/kg intraperitoneally injection) was used to induce diabetes. Four weeks after induction of diabetes, rats received crocin (50 mg/kg) and losartan (25 mg/kg) daily for four weeks orally. Rats were sacrificed at the end of the intervention, and blood samples were taken to determine serum levels of glucose, urea, creatinine (Cr), malondialdehyde (MDA), and thiol. Real-time polymerase chain reaction (PCR) was used to assess the expression of the FRMD3 and BMP7 genes in the kidney samples.
Diabetes induction increased serum levels of glucose, Cr, urea, MDA, and thiol, but decreased BMP7 and FRMD3 genes expression. Treatment with crocin and losartan decreased these biochemical parameters and increased the expression of the BMP7 and FRMD3 genes.
Crocin may be a promising therapeutic agent for preventing and improving diabetes-related kidney disease due to its antidiabetic and antioxidant properties.
糖尿病是一种多因素且不断增长的疾病,其严重并发症之一是糖尿病肾病(DN),这是慢性肾衰竭的最常见原因。FERM 结构域包含蛋白 3(FRMD3)负责维持肾单位细胞的形状和完整性,骨形态发生蛋白 7(BMP7)有助于维持功能并减少肾脏损伤。本研究旨在评估藏红花素和氯沙坦对链脲佐菌素(STZ)诱导的糖尿病大鼠生化参数和 FRMD3 和 BMP7 基因表达的影响。
将 40 只雄性 Wistar 大鼠随机分为五组:健康对照组(C)、糖尿病对照组(D)、藏红花素组(CR)、氯沙坦组(LA)和糖尿病大鼠联合治疗组(LA+CR),每组 8 只。大鼠一次性腹腔注射 STZ(50mg/kg)诱导糖尿病。糖尿病诱导 4 周后,大鼠分别给予藏红花素(50mg/kg)和氯沙坦(25mg/kg)每日灌胃 4 周。干预结束后处死大鼠,取血样检测血清中葡萄糖、尿素、肌酐(Cr)、丙二醛(MDA)和巯基的水平。实时聚合酶链反应(PCR)检测肾组织中 FRMD3 和 BMP7 基因的表达。
糖尿病诱导使血清中葡萄糖、Cr、尿素、MDA 和巯基的水平升高,而 BMP7 和 FRMD3 基因的表达降低。藏红花素和氯沙坦联合治疗降低了这些生化参数,并增加了 BMP7 和 FRMD3 基因的表达。
藏红花素可能具有抗糖尿病和抗氧化特性,有望成为预防和改善糖尿病相关肾病的治疗药物。