Giresun University, Faculty of Medicine, Department of Histology and Embryology, Giresun, Turkey.
Giresun University, Faculty of Medicine, Department of Gynaecology, Giresun, Turkey.
Biomed Pharmacother. 2019 Feb;110:742-747. doi: 10.1016/j.biopha.2018.12.037. Epub 2018 Dec 13.
This study aimed to investigate the protective effects of nigella sativa oil (NSO) against liver damage due to intraperitoneal (i.p.) usage of carboplatin which is commonly used as a chemotherapeutic agent.
Twenty four female Wistar-albino rats (about 200-350 grams each) were divided into 4 groups. Group 1 (n = 6) was administered 4 ml/kg intraperitoneal (i.p.) saline 48 and 24 h before. Group 2 (n = 6) was i.p. administered 4 ml/kg NSO 48 h before and 4 ml/kg saline 24 h before. Group 3 (n = 6) was i.p. administered 4 ml/kg saline 48 h before and 80 mg/kg carboplatin 24 h before. Group 4 (n = 6) was i.p. administered 4 ml/kg NSO 48 h before and 80 mg/kg carboplatin 24 h before. At the end of 48 h, all rats were sacrificed, and liver tissues were put into 10% neutral formalin. After the routine tissue follow-up, histopathological changes and collagen fiber density were evaluated with Hematoxylin-Eosin and Masson's Trichrome staining. Apoptotic index was determined with TUNEL staining.
The degeneration in hepatocytes, fiber distribution and density around central vein and portal space was observed in the carboplatin group compared to the control and NSO groups, hepatocyte cords preserved integrity, partial degeneration in hepatocytes and decreased collagen fiber distribution around central vein was noted in the NSO-carboplatin group compared to the carboplatin group. The apoptosis was lower in the NSO-carboplatin group compare with the carboplatin group, but no statistically significant difference was found between the two groups (p = 0.449).
When used NSO before carboplatin exposure, it may protect against liver damage.
本研究旨在探讨黑种草籽油(NSO)对腹腔内(i.p.)使用卡铂引起的肝损伤的保护作用,卡铂常作为化疗药物使用。
将 24 只雌性 Wistar 白化大鼠(每只约 200-350 克)分为 4 组。第 1 组(n=6)在给药前 48 小时和 24 小时腹腔内(i.p.)给予 4ml/kg 生理盐水。第 2 组(n=6)在给药前 48 小时腹腔内给予 4ml/kg NSO,并在 24 小时前给予 4ml/kg 生理盐水。第 3 组(n=6)在给药前 48 小时腹腔内给予 4ml/kg 生理盐水,24 小时前腹腔内给予 80mg/kg 卡铂。第 4 组(n=6)在给药前 48 小时腹腔内给予 4ml/kg NSO,24 小时前腹腔内给予 80mg/kg 卡铂。48 小时后,所有大鼠均被处死,肝组织置于 10%中性福尔马林。常规组织随访后,采用苏木精-伊红和 Masson 三色染色评估组织学变化和胶原纤维密度,采用 TUNEL 染色评估细胞凋亡指数。
与对照组和 NSO 组相比,卡铂组肝细胞变性、中央静脉和门腔周围纤维分布和密度增加,肝小叶保持完整,肝细胞部分变性,中央静脉周围胶原纤维分布减少。与卡铂组相比,NSO-卡铂组的细胞凋亡率较低,但两组间无统计学差异(p=0.449)。
在接触卡铂前使用 NSO 可能会预防肝损伤。