[Effect of Cynaropicrin on 2,3,4,7,8-Pentachlorodibenzofuran-induced Wasting Syndrome and Oxidative Stress].

Ken-ichi Yamada, Yuji Ishii, Tomoki Takeda, Hiroaki Kuroki, Chikage Mitoma, Hiroshi Uchi, Masutaka Furue, Hideyuki Yamada
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Abstract

The effect of cynaropicrin that is the major component of an edible plant, artichoke (Cynara scolymus) on 2,3,4,7,8-pentachlorodibenzofuran (PenCDF)-induced toxicity in mice was studied. We evaluated the effect of cynaropicrin on the wasting syndrome and oxidative stress elicited by PenCDF. However, the PenCDF dose-response relationship on the wasting syndrome has been superficial. Therefore, we determined the dose which causes wasting syndrome in C57BL/6J mice, a responsive strain to dioxins. Since 2,3,7,8-tetrachlorodibenzo-p-dioxin (0.1 mg/kg, p.o.) induces hepatic ethoxyresorfin O-deethylase (EROD) activity in mice, we set the doses of PenCDF at 0.3, 1.0, 3.0, 5.0 and 10 mg/kg (once, p.o.) on the basis of its toxic-eqivalency factor (0.3). The wasting syndrome was evaluated by measuring the daily changes of body weight. Thiobarbituric acid-reactive substances were used as an index of oxidative stress. Of PenCDF doses examined, wasting syndrome and oxidative stress took place most markedly in 5 mg/kg. In disagreement with this, EROD activity which is the marker of the aryl hydrocarbon receptor-dependent induction of cytochrome P450 1a1 was elevated most abundantly at 0.3 mg/kg. Then, we examined the effect of cynaropicrin on the wasting syndrome and oxidative stress provoked by PenCDF at 5 mg/kg. However, this compound up to 20 mg/kg (p.o.) did not attenuate PenCDF-induced wasting syndrome. On the contray, PenCDF-induced oxidateive stress was suppressed by cynaropicrin at the highest dose (20 mg/kg), although EROD activity was increased rather than reduced by cynaropicrin at lower doses. Thus, it is suggested that cynaropicrin has an ability to reduce oxidative stress caused by PenCDF.

[Cynaropicrin对2,3,4,7,8-五氯二苯并呋喃诱导的消耗综合征和氧化应激的影响]。
本文研究了食用植物朝鲜蓟(Cynara scolymus)的主要成分cynaropicrin对2,3,4,7,8-五氯二苯并呋喃(PenCDF)致小鼠毒性的影响。我们评价了辛诺苦苷对PenCDF引起的消耗综合征和氧化应激的影响。然而,在消耗综合征中,PenCDF的剂量-反应关系是肤浅的。因此,我们确定了引起二恶英反应品系C57BL/6J小鼠消耗综合征的剂量。由于2,3,7,8-四氯二苯并-对二恶英(0.1 mg/kg, p.o.)可诱导小鼠肝脏乙氧基间苯二酚o-去乙基酶(EROD)活性,我们根据其毒性当量因子(0.3)将PenCDF的剂量设定为0.3、1.0、3.0、5.0和10 mg/kg(1次,p.o.)。通过测量体重的每日变化来评估消耗综合征。硫代巴比妥酸反应物质作为氧化应激的指标。在所检测的PenCDF剂量中,消耗综合征和氧化应激在5 mg/kg时发生最明显。与此相反,作为芳烃受体依赖性诱导细胞色素P450 1a1的标志的EROD活性在0.3 mg/kg时显著升高。然后,我们研究了5 mg/kg剂量的辛诺苦苷对pendf引起的消耗综合征和氧化应激的影响。然而,该化合物高达20 mg/kg (p.o)并没有减轻pdf诱导的消耗综合征。相反,在最高剂量(20 mg/kg)下,辛纳苦苷抑制了pdf诱导的氧化应激,但在较低剂量下,辛纳苦苷增加而不是降低了EROD活性。因此,提示cynaropicrin具有降低PenCDF引起的氧化应激的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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