Forensic Medicine and Toxicology Department, Faculty of Veterinary Medicine, Zagazig University, Egypt.
Histology and Cytology Department, Faculty of Veterinary Medicine, Zagazig University, Egypt.
Ecotoxicol Environ Saf. 2020 Apr 1;192:110256. doi: 10.1016/j.ecoenv.2020.110256. Epub 2020 Jan 31.
The modulatory role of the Spirulina platensis (SP) against furan-induced (FU) hepatic and renal damage was assessed in this study. For achieving this, sixty rats were distributed into six groups: control group, SP-administered group (300 mg/kg b.wt orally for 28 days), a FU-intoxicated group (16 mg/kg b.wt, orally, daily for 28 days), protective co-treated group SP/F (administered SP 300 mg/kg b.wt, one week before, and concurrently with FU intoxication), therapeutic co-treated group FU/SP (administered SP 300 mg/kg b.wt, one week after FU intoxication for 28 days) and protective/therapeutic co-treated group SP/FU/SP (administered SP one week before and after, concurrently with FU intoxication). Subsequently, the biochemical responses and the histology of hepatic and renal tissues in treated rats were assessed. The results indicated that FU intoxication induced a significant hepato- and nephropathy represented by the elevation in the values of tissue injury biomarkers and reduction in protein levels. Histologically, a wide range of morphological, cytotoxic, inflammatory, and vascular alterations as well as downregulation in the immunoexpression of the proliferating cell nuclear antigen (PCNA) and the proliferation-associated nuclear antigen (Ki-67) were induced by FU intoxication. Oral SP administration, particularly in the protective/therapeutic co-treated group, markedly supressed the serum levels of the tissue injury biomarkers, diminished the inflammatory response, restored the cytotoxic alterations, upregulated the immunoexpression of PCNA and Ki-67, and restored the perturbed morphology of the hepatic and renal tissues. In conclusion, the obtained data demonstrated that SP co-administration elicits both protective and therapeutic potential against the FU-induced hepato- and nephropathy.
本研究评估了螺旋藻(SP)对呋喃诱导(FU)肝和肾损伤的调节作用。为此,将 60 只大鼠分为 6 组:对照组、SP 给药组(300mg/kg bw 口服,28 天)、FU 中毒组(16mg/kg bw,口服,每天 1 次,28 天)、SP/F 保护共处理组(SP 给药 300mg/kg bw,1 周前和 FU 中毒同时)、FU/SP 治疗共处理组(FU 中毒 1 周后给予 SP 300mg/kg bw,28 天)和 SP/FU/SP 保护/治疗共处理组(1 周前和 FU 中毒同时给予 SP)。随后,评估了治疗大鼠的生化反应和肝、肾组织的组织学变化。结果表明,FU 中毒引起明显的肝和肾病,表现为组织损伤生物标志物的升高和蛋白质水平的降低。组织学上,FU 中毒引起广泛的形态学、细胞毒性、炎症和血管改变,以及增殖细胞核抗原(PCNA)和增殖相关核抗原(Ki-67)的免疫表达下调。口服 SP 给药,特别是在保护/治疗共处理组,显著抑制血清组织损伤生物标志物水平,减轻炎症反应,恢复细胞毒性改变,上调 PCNA 和 Ki-67 的免疫表达,并恢复肝、肾组织的形态改变。总之,研究结果表明,SP 共给药对 FU 诱导的肝和肾病具有保护和治疗作用。