Qian Weibin, Cai Xinrui, Wang Yingying, Zhang Xinying, Zhao Hongmin, Qian Qiuhai, Yang Zhihong, Liu Zhantao, Hasegawa Junichi
Division of Pharmacotherapeutics, Department of Pathophysiological and Therapeutic Science, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8503, Japan; †Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan 250011, Shandong, China.
‡Shandong Academy Occupational Health and Occupational Medicine, Shandong Academy of Medical Sciences, Jinan 250002, Shandong, China.
Yonago Acta Med. 2016 Jun 29;59(2):100-10. eCollection 2016 Jun.
Gingerol, the generic term for pungent constituents in ginger, has been used for treating vomiting in China. We are going to investigate the mechanisms of inhibitive effect of gingerol on cisplatin-induced pica behaviour by studying on both peripheral and central levels, and the effects of gingerol on homeostasis of dopamine (DA) transmission: dopamine D2 receptor (D2R), dopamine transporter (DAT) and tyrosine hydroxylase (TH).
The antiemetic effect of gingerol was investigated on a vomiting model in rats induced by cisplatin 3 mg·kg(-1) intraperitoneal injection (i.p.). Rats were randomly divided into the normal control group (C), simple gingerol control group (CG), cisplatin control group (V), cisplatin + metoclopramide group (M), cisplatin + low-dose gingerol group (GL), cisplatin + middle-dose gingerol group (GM) and cisplatin + high-dose gingerol group (GH). In observation period, rats in Groups C and V were pretreated with sterile saline 3 mL i.g.; rats in Group CG were pretreated with gingerol 40 mg·kg(-1) i.g.; rats in Group M were pretreated with metoclopramide 2.5 mg·kg(-1) i.g.; rats in Groups GL, GM and GH were pretreated with gingerol 10, 20 and 40 mg·kg(-1) i.g. for 3 days, respectively. Cisplatin (3 mg·kg(-1), i.p.) was administered one time after each treatment with the antiemetic agent or its vehicle except the Groups C and CG. The distribution of D2R, DAT and TH in the area postrema and ileum were measured by immunohistochemistry and quantitated based on the image analysis, and the expression of DAT and TH in the area postrema and ileum were measured by RT-PCR. The weights of kaolin eaten of the remaining rats were observed in every 6 h continuously for 72 h.
The weight of kaolin eaten in rats induced by cisplatin was significantly reduced by pretreatment with gingerol in a dose-dependent manner during the 0-24 h and 24-72 h periods (P < 0.05). Gingerol markedly improved gastric emptying induced by cisplatin in a dose-dependent manner (P < 0.05), and exhibited effective dose-dependent inhibition on the increase of expression levels of D2R and TH and the decrease of expression levels of DAT in both the ileum and area postrema (P < 0.05).
Gingerol is effective on cisplatin-induced emesis in rats possibly by inhibiting central or peripheral increase of DA by inhibiting D2R, TH and accelerating DAT.
姜辣素是生姜中辛辣成分的统称,在中国一直用于治疗呕吐。我们将通过外周和中枢水平的研究,探讨姜辣素对顺铂诱导的异食行为的抑制作用机制,以及姜辣素对多巴胺(DA)传递稳态的影响:多巴胺D2受体(D2R)、多巴胺转运体(DAT)和酪氨酸羟化酶(TH)。
采用腹腔注射3mg·kg⁻¹顺铂诱导大鼠呕吐模型,研究姜辣素的止吐作用。将大鼠随机分为正常对照组(C)、单纯姜辣素对照组(CG)、顺铂对照组(V)、顺铂+甲氧氯普胺组(M)、顺铂+低剂量姜辣素组(GL)、顺铂+中剂量姜辣素组(GM)和顺铂+高剂量姜辣素组(GH)。在观察期内,C组和V组大鼠经口给予3mL无菌生理盐水预处理;CG组大鼠经口给予40mg·kg⁻¹姜辣素预处理;M组大鼠经口给予2.5mg·kg⁻¹甲氧氯普胺预处理;GL、GM和GH组大鼠分别经口给予10、20和40mg·kg⁻¹姜辣素预处理3天。除C组和CG组外,每次给予止吐剂或其溶媒后,腹腔注射一次顺铂(3mg·kg⁻¹)。采用免疫组织化学法检测延髓后区和回肠中D2R、DAT和TH的分布,并基于图像分析进行定量,采用RT-PCR法检测延髓后区和回肠中DAT和TH的表达。连续72小时,每6小时观察剩余大鼠高岭土摄食量。
在0-24小时和24-72小时期间,姜辣素预处理可使顺铂诱导的大鼠高岭土摄食量显著降低,且呈剂量依赖性(P<0.05)。姜辣素能显著改善顺铂诱导的胃排空,且呈剂量依赖性(P<0.05),并对回肠和延髓后区D2R和TH表达水平的升高以及DAT表达水平的降低具有有效的剂量依赖性抑制作用(P<0.05)。
姜辣素对顺铂诱导的大鼠呕吐有效,可能是通过抑制D2R、TH,加速DAT,从而抑制中枢或外周DA的增加。