菊苣提取物对重铬酸钾处理大鼠部分生化指标及甲状腺激素的影响

E. Abdel-Baky, K. Gomaa
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引用次数: 0

摘要

菊苣(菊苣intybus L.)的叶子被用作食物补充剂和传统药物。研究菊苣叶提取物对大鼠重铬酸钾中毒的保护作用。实验选用雄性大鼠24只,随机分为4组,每组6只。第一组作为对照组,每天口服1 ml蒸馏水,连续4周,然后在斩首前24小时腹腔注射1 ml生理盐水溶液。组2为K2Cr2O7−处理组;每天口服蒸馏水1 ml,连续4周,然后在斩首前24小时静脉注射单剂量K2Cr2O7 (30 mg/kg体重,静脉注射)。第三组为菊苣治疗组,给予菊苣提取物(250 mg/kg体重,每日,连用4周)口服,并于斩首前24小时静脉注射生理盐水1 ml(1次)。第4组在斩首前24小时腹腔注射单剂量K2Cr2O7 (30 mg/kg体重),口服菊苣提取物(250 mg/kg体重,每日,连续4周)。重铬酸钾诱导血清中促甲状腺激素(TSH)、葡萄糖、总胆固醇(TC)、低密度脂蛋白胆固醇(LDL - C)、总胆固醇/高密度脂蛋白胆固醇(TC/HDL - C)比值、LDL - C/HDL - C比值和甘油三酯(TG)水平显著升高,淀粉酶和脂肪酶活性显著升高。而K2Cr2O7 -处理组血清中游离三碘甲状腺原氨酸(FT3)、甲状腺素(FT4)、胰岛素和HDL - C水平显著降低。菊苣提取物单独处理可显著降低大鼠血清FT4、TC、LDL - C、HDL - C、TC/HDL - C和LDL - C/HDL - C水平,显著提高血清淀粉酶活性。在K2Cr2O7治疗前给予菊石提取物可在一定程度上中和K2Cr2O7对血清FT3、FT4、TSH、葡萄糖、胰岛素、总胆固醇、LDL - C、HDL - C、TC/HDL - C、LDL - C/HDL - C、TG水平以及淀粉酶和脂肪酶活性的有害影响。综上所述,菊苣提取物可调节K2Cr2O7中毒大鼠的生化指标和甲状腺激素的变化。
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EFFECTS OF CICHORIUM INTYBUS L. EXTRACT ON SOME BIOCHEMICAL PARAMETERS AND THYROID HORMONES IN POTASSIUM DICHROMATE TREATED RATS
Chicory (Cichorium intybus L.) leaves are used as food supplement and also in traditional medicine. The objective of this research was to determine the protective ability of chicory leaves extract against the toxicity induced by potassium dichromate in rats. Twenty four male rats were used in the present study and classified randomly into four groups (6 rats per group). The first group was served as a control and was given orally 1 ml of distilled water daily for four weeks, then injected intraperitoneally (i.p.) with 1 ml of saline solution 24 hours prior to decapitation. Group 2 was the K2Cr2O7−treated group; it received orally 1 ml of distilled water daily for four weeks, then i.p. injected with a single dose of  K2Cr2O7 (30 mg/kg body weight, i.p.) 24 hours prior to decapitation. Group 3 was chicory treated group and was given orally chicory extract (250 mg/kg body weight, daily for four weeks), then injected with 1 ml saline solution (i.p.) 24 hours prior to decapitation. Group 4 received orally chicory extract (250 mg/kg body weight, daily for four weeks) prior to i.p. injection with a single dose of K2Cr2O7 (30 mg/kg body weight 24 hours before decapitation). Potassium dichromate induced a significant elevation in the levels of thyroid stimulating hormone (TSH), glucose, total cholesterol (TC), low−density lipoprotein cholesterol (LDL−C), total cholesterol/high-density lipoprotein cholesterol (TC/HDL−C) ratio, LDL−C/HDL−C ratio and trigylcerides (TG), as well as the activities of amylase and lipase enzymes in serum. Whereas, there is a significant decrease in free tri-iodothyronine (FT3), thyroxine (FT4), insulin and HDL−C levels in serum of K2Cr2O7−treatedrats. Treatment of rats with chicory extract alone decreased significantly the levels of serum FT4, TC, LDL−C, HDL−C, TC/HDL−C and LDL−C/HDL−C, while it increased significantly the amylase serum activity. The administration of chicory extract before the treatment with K2Cr2O7 could neutralize, to some extent, the harmful effects of K2Cr2O7 on the serum FT3, FT4, TSH, glucose, insulin, total cholesterol, LDL−C, HDL−C, TC/HDL−C, LDL−C/HDL−C and TG levels, as well as the activities of amylase and lipase enzymes. In conclusion, the results showed that the chicory extract may modulate changes in the biochemical parameters and thyroid hormones that were induced by K2Cr2O7 toxicity in rats.
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