Supapom Chunchom, Teeraporn Katisart, Sirirat Deeseenthum, C. Talubmook
{"title":"糙米开菲尔粉的急性毒性","authors":"Supapom Chunchom, Teeraporn Katisart, Sirirat Deeseenthum, C. Talubmook","doi":"10.1109/TICST.2015.7369350","DOIUrl":null,"url":null,"abstract":"Kefir is a fermented milk product comprising several lactic acid bacteria, acetic acid bacteria and yeasts. It has been reported to possess pharmacological and antioxidant activities. Recently, kefir from rice milk showed antioxidant activity higher than that from cow milk. To see whether rice and rice products such as rice kefir is safe for human applications. Therefore, the present study was designed to determine an acute toxicity of kefir powder from brown rice; KhaoDawk Mali 105 (KDMLKP), Red Hawm (RHKP) and Hawm Nil (HNKP). The study was carried out in male Wistar rats by once giving kefir powder at the doses of 1,000, 2,000 and 4,000 mg/kg to the rats orally. The results showed that the kefir powder of all the doses did not produce mortality and symptoms of toxicity. Moreover, the kefir powder did not alter relative organ weight (ROW) and feed conversion ratio (FCR) in the kefir powder treated rats compared to those in controls, but this was not a 4,000 mg/kg RHKP. Increasing KDMLKP significantly (p≤0.05) increased body weight gain and food intake, whilst increasing HNKP significantly (p≤0.05) decreased the body weight gain, but significantly (p≤0.05) increased food intake in the treated rats compared to that in controls. However, RHKP did not alter the body weight gain but increasing RHKP significantly (p≤0.05) decreased food intake in the treated rats compared to that in controls. KDMLKP and HNKP did not alter BS, BUN, CREA, UA, TP, Alb, AST, ALT, and ALP in the treated rats compared to those in controls. KDMLKP at a dose of 4,000 mg/kg significantly (p≤0.05) increased TP and Alb. Nevertheless, RHKP at a dose of 4,000 mg/kg significantly (p≤0.05) increased BUN, TP, AST, ALT, and ALP in the treated rats when compared to those in controls. KDMLKP, RHKP and HNKP did not alter WBC, Hb, Hct and Plt in the treated rats compared to those in controls but this was not at a dose of 4,000 mg/kg RHKP. Interestingly, the rats received 4,000 mg/kg KDMLKP and RHKP but not HNKP significantly (p≤0.05) reduced RBC compared to that in controls. Moreover, increasing KDMLKP, RHKP and HNKP significantly (p≤0.05) decreased Neu but increased Lym compared to those in controls. These findings indicate that the kefir powder from brown rice; KhaoDawk Mali 105 (KDMLKP), Red Hawm (RHKP) and Hawm Nil (HNKP) exhibit non acute toxicity with LD50 higher than 4,000 mg/kg. 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Therefore, the present study was designed to determine an acute toxicity of kefir powder from brown rice; KhaoDawk Mali 105 (KDMLKP), Red Hawm (RHKP) and Hawm Nil (HNKP). The study was carried out in male Wistar rats by once giving kefir powder at the doses of 1,000, 2,000 and 4,000 mg/kg to the rats orally. The results showed that the kefir powder of all the doses did not produce mortality and symptoms of toxicity. Moreover, the kefir powder did not alter relative organ weight (ROW) and feed conversion ratio (FCR) in the kefir powder treated rats compared to those in controls, but this was not a 4,000 mg/kg RHKP. Increasing KDMLKP significantly (p≤0.05) increased body weight gain and food intake, whilst increasing HNKP significantly (p≤0.05) decreased the body weight gain, but significantly (p≤0.05) increased food intake in the treated rats compared to that in controls. However, RHKP did not alter the body weight gain but increasing RHKP significantly (p≤0.05) decreased food intake in the treated rats compared to that in controls. KDMLKP and HNKP did not alter BS, BUN, CREA, UA, TP, Alb, AST, ALT, and ALP in the treated rats compared to those in controls. KDMLKP at a dose of 4,000 mg/kg significantly (p≤0.05) increased TP and Alb. Nevertheless, RHKP at a dose of 4,000 mg/kg significantly (p≤0.05) increased BUN, TP, AST, ALT, and ALP in the treated rats when compared to those in controls. KDMLKP, RHKP and HNKP did not alter WBC, Hb, Hct and Plt in the treated rats compared to those in controls but this was not at a dose of 4,000 mg/kg RHKP. Interestingly, the rats received 4,000 mg/kg KDMLKP and RHKP but not HNKP significantly (p≤0.05) reduced RBC compared to that in controls. Moreover, increasing KDMLKP, RHKP and HNKP significantly (p≤0.05) decreased Neu but increased Lym compared to those in controls. These findings indicate that the kefir powder from brown rice; KhaoDawk Mali 105 (KDMLKP), Red Hawm (RHKP) and Hawm Nil (HNKP) exhibit non acute toxicity with LD50 higher than 4,000 mg/kg. 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引用次数: 4
摘要
开菲尔是一种由乳酸菌、醋酸菌和酵母组成的发酵乳制品。据报道,它具有药理和抗氧化活性。近年来,米乳克非尔的抗氧化活性高于牛奶。看看大米和米制品,如米开菲尔,对人类是否安全。因此,本研究旨在确定糙米开菲尔粉的急性毒性;KhaoDawk Mali 105 (KDMLKP), Red Hawm (RHKP)和Hawm Nil (HNKP)。本研究以雄性Wistar大鼠为研究对象,分别口服1,000、2,000和4,000 mg/kg剂量的开菲尔粉。结果表明,所有剂量的开菲尔粉均未产生死亡和毒性症状。此外,与对照组相比,克非尔粉没有改变克非尔粉处理大鼠的相对器官重量(ROW)和饲料转化率(FCR),但这不是4000 mg/kg RHKP。增加KDMLKP显著(p≤0.05)提高了治疗组大鼠的增重和摄食量,增加HNKP显著(p≤0.05)降低了治疗组大鼠的增重,但显著(p≤0.05)增加了治疗组大鼠的摄食量。然而,RHKP对体重增加没有影响,但RHKP的增加显著(p≤0.05)降低了治疗大鼠的摄食量。与对照组相比,KDMLKP和HNKP未改变治疗大鼠的BS、BUN、CREA、UA、TP、Alb、AST、ALT和ALP。4000 mg/kg剂量的KDMLKP显著(p≤0.05)提高TP和Alb。然而,与对照组相比,4000 mg/kg剂量的RHKP显著(p≤0.05)提高了治疗大鼠的BUN、TP、AST、ALT和ALP。与对照组相比,KDMLKP、RHKP和HNKP没有改变治疗大鼠的WBC、Hb、Hct和Plt,但这不是在剂量为4000 mg/kg RHKP时发生的。有趣的是,与对照组相比,接受4000 mg/kg KDMLKP和RHKP治疗的大鼠红细胞明显减少(p≤0.05)。与对照组相比,增加KDMLKP、RHKP和HNKP显著(p≤0.05)降低了Neu,提高了Lym。结果表明:糙米开菲尔粉;红山楂105 (KDMLKP)、红山楂(RHKP)和红山楂零(HNKP)表现出非急性毒性,LD50高于4000 mg/kg。从这种糙米中提取的开菲尔粉可能是一种新的良好的营养资源。
Kefir is a fermented milk product comprising several lactic acid bacteria, acetic acid bacteria and yeasts. It has been reported to possess pharmacological and antioxidant activities. Recently, kefir from rice milk showed antioxidant activity higher than that from cow milk. To see whether rice and rice products such as rice kefir is safe for human applications. Therefore, the present study was designed to determine an acute toxicity of kefir powder from brown rice; KhaoDawk Mali 105 (KDMLKP), Red Hawm (RHKP) and Hawm Nil (HNKP). The study was carried out in male Wistar rats by once giving kefir powder at the doses of 1,000, 2,000 and 4,000 mg/kg to the rats orally. The results showed that the kefir powder of all the doses did not produce mortality and symptoms of toxicity. Moreover, the kefir powder did not alter relative organ weight (ROW) and feed conversion ratio (FCR) in the kefir powder treated rats compared to those in controls, but this was not a 4,000 mg/kg RHKP. Increasing KDMLKP significantly (p≤0.05) increased body weight gain and food intake, whilst increasing HNKP significantly (p≤0.05) decreased the body weight gain, but significantly (p≤0.05) increased food intake in the treated rats compared to that in controls. However, RHKP did not alter the body weight gain but increasing RHKP significantly (p≤0.05) decreased food intake in the treated rats compared to that in controls. KDMLKP and HNKP did not alter BS, BUN, CREA, UA, TP, Alb, AST, ALT, and ALP in the treated rats compared to those in controls. KDMLKP at a dose of 4,000 mg/kg significantly (p≤0.05) increased TP and Alb. Nevertheless, RHKP at a dose of 4,000 mg/kg significantly (p≤0.05) increased BUN, TP, AST, ALT, and ALP in the treated rats when compared to those in controls. KDMLKP, RHKP and HNKP did not alter WBC, Hb, Hct and Plt in the treated rats compared to those in controls but this was not at a dose of 4,000 mg/kg RHKP. Interestingly, the rats received 4,000 mg/kg KDMLKP and RHKP but not HNKP significantly (p≤0.05) reduced RBC compared to that in controls. Moreover, increasing KDMLKP, RHKP and HNKP significantly (p≤0.05) decreased Neu but increased Lym compared to those in controls. These findings indicate that the kefir powder from brown rice; KhaoDawk Mali 105 (KDMLKP), Red Hawm (RHKP) and Hawm Nil (HNKP) exhibit non acute toxicity with LD50 higher than 4,000 mg/kg. Kefir powder from this brown rice is probably a new good nutrition resource.