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1.
为探讨氟化钠对幼年大鼠血清4种微量元素和骨矿物质含量的影响,以及大鼠骨矿物质和血清微量元素的相关性,将80只2月龄SPF级SO大鼠,雌雄各半,随机分成8组:对照(幼年CS、成年AS)组和用药组(幼年高氟组CHS、幼年低氟组CLS、成年高氟组AHS、成年低氟组ALS、幼年长期高氟组HS、幼年长期低氟组15)。对照组灌胃生理盐水,用药组分别按相应时间给予不同剂量的NaF灌胃,测定了大鼠尺骨和血清中的Ca、P、Fe、Zn含量。结果表明,(1)血清微量元素:①与cs组相比,CHS组和CLS组的磷(P)分别增加100.0%和193.8%(P〈0.05)。②与AS组相比,HS组的Ca、Zn分别下降了20.5%和40.0%,而P则增加了74.0%(P〈0.05);Ls组的Zn下降了33.3%(P〈0.05)。与HS组比较,CHS组的Ca增加22.3%。③与LS组比较,CLS组的P和Zn明显增加49.2%和28.5%(P〈0.05)。(2)骨矿物质:①与As组相比,HS组的Ca分别下降了23.9%(P〈0.05),Zn则增加了36.1%(P〈0.05)。②与HS组相比,CHS组的Ca和Fe分别增加了42.3%和36.05%,Zn下降了38.6%(P〈0.05)。(3)骨矿物质和血清微量元素的相关性:骨Ca和血Ca、骨P和血P、骨Zn和血Zn、骨Fe和血Fe的相关系数分别为0.435、0.347、0.136和0.059(P〉0.05)。提示长期使用氟化钠,可以导致幼年大鼠血中微量元素代谢紊乱,骨矿物含量降低,但未确定大鼠骨矿物含量和血微量元素具有相关性。  相似文献   

2.
为探讨氟化钠对雄性小鼠精子畸形的影响,选取50只成年雄性小鼠随机分为5组:氟化钠染毒高剂量组(34mg/kg)、中剂量组(17mg/kg)、低剂量组(8.5mg/kg)、环磷酰胺阳性对照组(50mg/kg)、生理盐水空白对照组,采用经口灌胃染毒,1次/d,连续5d,于首次染毒后的第35天颈椎脱臼将小鼠处死,取睾丸和附睾称质量,计算脏器系数;同时取附睾制片,观察精子形态,计数小鼠精子畸形率。结果表明,氟化钠染毒各组睾丸、附睾脏器系数与空白对照组比较,差别无统计学意义(P〉0.05),染毒各组精子畸形率普遍高于空白对照组,差别有统计学意义(P〈0.001),且随着染毒剂量的增加精子畸形率也有相应升高,呈现一定的剂量一反应关系(r=0.954,F=20.098,P〈0.05,R^2=0.909)。提示氟化钠能使雄性小鼠精子畸形率明显升高,具有一定的生殖毒性,能影响小鼠生殖功能,对小鼠生殖功能造成损害。  相似文献   

3.
用测定骨元素含量的方法,观察了运动对氟化钠(NaF)抗去卵巢大鼠骨元素代谢的影响效应。将健康4月龄雌性SD大鼠30只,用抽签法随机分成5组:正常对照组,假去卵巢组,去卵巢组,去卵巢+NaF组和去卵巢+NaF+运动组;去卵巢+NaF组和去卵巢+NaF+运动组大鼠于去卵巢手术后第2天开始给予NaF溶液灌胃,1mg/(kg·BW),1次/d,持续11周;去卵巢+NaF+运动组大鼠于去卵巢术后第7天开始运动训练,每周5d,每天连续匀速跑45min,16m/min,跑道倾角0。,持续10周。结果表明,去卵巢大鼠骨Ca、S、Mg、Zn、Co、Mn等元素含量显著降低,骨P含量增加;NaF可使去卵巢大鼠降低的骨Ca、S、Mg、Co、Mn等元素含量回升,骨P含量回降;运动与NaF联合应用能使骨Ca、S、Mg、Zn、Co、Mn等元素含量显著回升,骨P含量显著回降。提示运动可加强NaF对抗由于去卵巢引起的大鼠骨元素代谢紊乱的作用。  相似文献   

4.
为探讨两种形式有机铬吡啶羧酸铬(CrPic)和烟酸铬(CrNic)改善SD大鼠体组成的效果及其机制,将60只雄性SD大鼠随机等分为3组,第1组饲喂基础日粮作为对照组,第2和第3组分别以CrPic和CrNic形式添加300μg/kg铬,自由采食和饮水,6周后测定大鼠体组成和皮下脂肪组织中脂肪酸合成酶及激素敏感酯酶活性以及血清相关指标。结果表明,添加CrPic使大鼠瘦体质量提高了21.9%(P〈0.05),体脂含量降低了22.6%(P〈0.05);添加CrNic对大鼠瘦体质量和体脂含量没有产生显著影响(P〉0.05);CrPic使大鼠皮下脂肪组织中脂肪酸合成酶活性降低了5.6%(P〈0.05),激素敏感酯酶活性提高了63.1%(P〈0.05),同时,大鼠血清中葡萄糖和胰岛素水平显著降低;CrNic对皮下脂肪组织中脂肪酸合成酶、激素敏感酯酶活性以及血清相关指标没有产生显著影响(P〉0.05)。提示CrPic能通过减弱机体脂肪合成代谢,增强脂肪分解代谢从而提高大鼠瘦体质量,降低体脂含量,其效果显著高于CrNic。  相似文献   

5.
采用多因素造模方法复制成湿热证动物模型,观察了动物模型微量元素Zn、Cu、Fe、Se和维生素E代谢水平的变化。结果显示,模型动物血清Zn下降(P<0.05),Cu升高(P<0.05或P<0.01),Fe变化不大(P>0.05),血Se水平下降(P<0.05),血浆维生素E含量减少(P<0.01)。经清热祛湿的经验方清香散治疗后,治疗I组动物血清Zn、血Se、血浆维生素E明显升高(P<0.05),血清Cu下降(P<0.05);治疗Ⅱ组血浆血清Cu有变化(P<0.05)外,其余变化不大。  相似文献   

6.
高硒情况下维生素E对老龄大鼠血清中抗氧化作用的影响   总被引:3,自引:0,他引:3  
研究了高Se或高维生素E下,老龄大鼠体内抗氧化活性的变化以及高Se下维生素E对其体内抗氧化水平的影响。将十二月龄Wistar大鼠32只随机分成4组:(1)正常饲料组;(2)高Se饲料组;(3)高维生素E饲料组;(4)高Se高维生素E饲料组。饲至十周末,处死大鼠,按试剂盒要求取其血液制成血清测GSH-Px,SOD活性,MDA含量。结果表明,高Se或高维生素E下饲养下的大鼠与对照组比较,血清中GSH-Px活性升高(P<0.05)。SOD活性未见改变,MDA含量分别减少50%和56%,有显著差异(P<0.01);维生素E与高Se合用与高Se组比较能进一步同GSH-Px,SOD活性(P<0.01)。结论:高Se会升高老龄大鼠的抗氧化活性,而与维生素E合用更加升高老龄大鼠血液中抗氧化活性。  相似文献   

7.
采用亚急性试验,探讨对二氯苯(P—DCB)对小鼠组织中Zn、Cu、Fe的影响。选用36只小鼠,雌雄各半,随机分成3组,每组12只,分别给予P—DCBO(对照组)、450、900mg·kg^-1,每天灌胃染毒1次,连续7d,染毒结束后24h处死动物并称体质量、肝、肾质量,计算脏器系数。用火焰原子吸收法测定肝脏、血液和肾脏中Zn、Cu、Fe含量。与对照组相比,各染毒组体质量无明显变化。各组肝体系数无差异,但染毒组肾体系数明显高于对照组(P〈O.05)。900mg·kg^-1组肝脏中Zn含量及w(Zn)/w(Cu)值较450mg·kg^-1组有明显升高。与对照组相比,各染毒组血液中Zn含量呈现下降趋势,900nag·kg^-1组较对照组明显下降(P〈0.05)。900mg·kg^-1组肾脏中Cu质量分数明显低于450mg·kg^-1组,Fe质量分数则较对照组及450mg·kg^-1组均有降低,P—DCB可影响小鼠组织中元素Zn、Cu、Fe的含量及不同器官的再分布,提示微量元素失衡可能是P—DCB毒作用的重要机制。  相似文献   

8.
为观察二硫化碳(CS2)对机体铜,锌水平的影响,对某化纤厂35名接触CS2工人和41名非接触工人的血铜,锌值进行调查,比较,并进行了动物染毒实验。SD大鼠吸入CS2浓度分别为5和50mg/m^3,每日5h,每周6d,连续6个月,于染毒2,4,6个月时测定血浆铜,锌值及染毒6个月时肝脏铜,锌含量。结果显示,CS2接触组工人血铜,锌水平较对照组显著降低(P<0.05)。在CS2染毒6个月时,50mg/m^3 CS2染毒组血浆及肝脏铜水平均较对照组及5mg/m^3 CS2染毒组显著降低(P<0.05)。可见接触CS2能干扰机体铜,锌代谢,导致体内铜,锌含量减少。  相似文献   

9.
营养性驱铅饮料对铅致骨髓细胞微核异常的防治大鼠研究结果表明:铅料组饮铅[659mg/(kg.d)]连续3月后,平均骨髓细胞微核千分率高达9.75,平均血铅高达3.69±0.05μmol/L,体重仅为216.9±24.6g。而饮料组[铅:659mg/(kg·d)+饮料]大鼠平均骨髓细胞微核千分率为5.22,与铅料组相比差异有高度显著性(P<0.01),与空白对照组(3.94‰)相近(P<0.05);平均血钳浓度(1.58±0.05μmol/L)也较铅料组低(P<0.01),而体重(278.1±73.0g)则较铅料组高(P<0.01),而与空白对照组(287.9±100.1g)相近(P>0.05)。提示:营养性驱铅饮料防治铅致骨髓细胞微核异常有明显效果,且能促进机体正常发育。  相似文献   

10.
慢性肺心病患者血清Cu,Zn及Cu/Zn比值的分析研究   总被引:1,自引:1,他引:1  
分析了65例慢性肺心病患者血清Cu,Zn的含量及Cu/Zn比值,并与健康对照组比较。结果显示,慢性肺心病患者组血清Zn的含量与健康对照组比较有高度显著性差异(P<0.01),Cu的含是有显著性差异(P<0.05),Cu/Zn比值有显著性差异(P<0.05)。提示慢性肺心病与微量元素Cu、Zn元素的含量变化有一定的关系,为研究元素医学与治疗慢性肺心病提供了必要的依据。  相似文献   

11.
Current anti-gastric ulcer agents have side effects, despite the progression and expansion of advances in treatment. This study aimed to investigate the gastroprotective mechanisms of Pithecellobium jiringa ethanol extract against ethanol-induced gastric mucosal ulcers in rats. For this purpose, Sprague Dawley rats were randomly divided into five groups: Group 1 (normal control) rats were orally administered with vehicle (carboxymethyl cellulose), Group 2 (ulcer control) rats were also orally administered with vehicle. Group 3 (positive control) rats were orally administered with 20 mg/kg omeprazole, Groups 4 and 5 (experimental groups) received ethanol extract of Pithecellobium jiringa ethanol extract at a concentration of 250 and 500 mg/kg, respectively. Sixty minutes later, vehicle was given orally to the normal control group, and absolute ethanol was given orally to the ulcer control, positive control and experimental groups to generate gastric mucosal injury. The rats were sacrificed an hour later. The effect of oral administration of plant extract on ethanol-induced gastric mucosal injury was studied grossly and histology. The level of lipid peroxidation (malondialdehyde-MDA), superoxide dismutase (SOD) and gastric wall mucus were measured from gastric mucosal homogenate. The ulcer control group exhibited severe gastric mucosal injury, and this finding was also confirmed by histology of gastric mucosa which showed severe damage to the gastric mucosa with edema and leucocyte infiltration of the submucosal layer. Pre-treatment with plant extract significantly reduced the formation of ethanol-induced gastric lesions, and gastric wall mucus was significantly preserved. The study also indicated a significant increase in SOD activity in gastric mucosal homogenate, whereas a significant decrease in MDA was observed. Acute toxicity tests did not show any signs of toxicity and mortality up to 5 g/kg. The ulcer protective effect of this plant may possibly be due to its preservation of gastric wall mucus along with increased SOD activity and reduction of oxidative stress (MDA). The extract is non-toxic, even at relatively high concentrations.  相似文献   

12.
地黄滋阴补血填髓,广泛用于贫血和脑疾病患者,但其功效机制尚未阐明.本文探讨地黄水提物(Rehmannia glutinosa’s water extracts,RGWE)改善血虚大鼠记忆及其滋阴补血填髓的可能机制.采用断尾放血结合注射环磷酰胺制备贫血大鼠模型,随机分溶媒组和地黄水提物3,6,10g/kg治疗组,灌服等体积自来水或不同剂量地黄水提物10天,采用Morris水迷宫观测大鼠空间记忆能力,采用酶联免疫吸附测定方法(Enzyme linked immunosorbent assay,ELISA)检测血浆红细胞生成素(EPO)水平,免疫组化和免疫蛋白印迹技术(Western blotting)检测分析脑EPO及其受体表达水平.成功制备血虚模型,表现为大鼠红细胞数和血红蛋白显著下降,与造模前比较差异显著(P<0.05),溶媒组空间记忆能力显著下降,地黄治疗组空间记忆能力明显提高,逃避潜伏期明显缩短(P<0.05),一定时间内穿越平台次数显著增多(P<0.05);免疫组化和Western blotting结果显示脑组织EPO及其受体表达、血浆EPO水平均较溶媒组明显升高(P<0.05).地黄水提物显著提高贫血...  相似文献   

13.
The study was aimed to investigate the effects of single and multiple oral administration of mungbean (Phaseolus radiatus L.) seed extract (ME) on the pharmacokinetics of aconitine in rats. The Sprague–Dawley rats were randomly divided into three groups (six rats each group). In group 1, rats were orally administered 500 µg/kg aconitine after receiving a single oral dose of 1 g/kg ME. In group 2, rats were orally administered with 500 µg/kg aconitine at day 7 of treatment with 1 g/kg/day ME. In group 3, rats were orally administered with 500 µg/kg aconitine. Blood samples were collected at different time points (0.083, 0.25, 0.5, 1.0, 1.5, 2.0, 4.0, 6.0, 8.0 and 10.0 h). The concentration of aconitine in rats plasma was determined by a fully validated ultra‐high‐performance liquid chromatography coupled with mass spectrometry method. The results showed that single and multiple oral co‐administration of ME significantly altered the pharmacokinetic parameters of aconitine. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

14.
Indolic compounds have attracted a lot of attention due to their interesting biological properties. The present study was performed to evaluate the subacute toxicity and anti-ulcer activity of BClHC against ethanol-induced gastric ulcers. Experimental animal groups were orally pre-treated with different doses of BClHC (50, 100, 200 and 400 mg/kg) in 10% Tween 20 solution (vehicle). Blank and ulcer control groups were pre-treated with vehicle. The positive group was orally pretreated with 20 mg/kg omeprazole. After one hour, all groups received absolute ethanol (5 mL/kg) to generate gastric mucosal injury except the blank control group which was administered the vehicle solution. After an additional hour, all rats were sacrificed, and the ulcer areas of the gastric walls determined. Grossly, the ulcer control group exhibited severe mucosal injury, whereas pre-treatment with either derivative or omeprazole resulted in significant protection of gastric mucosal injury. Flattening of gastric mucosal folds was also observed in rats pretreated with BClHC. Histological studies of the gastric wall of ulcer control group revealed severe damage of gastric mucosa, along with edema and leucocytes infiltration of the submucosal layer compared to rats pre-treated with either BClHC or omeprazole where there were marked gastric protection along with reduction or absence of edema and leucocytes infiltration of the submucosal layer. Subacute toxicity study with a higher dose of derivative (5 g/kg) did not manifest any toxicological signs in rats. In conclusions, the present finding suggests that benzyl N'-(5-chloroindol-3-ylmethylidene)hydrazinecarbodithioate promotes ulcer protection as ascertained by the comparative decreases in ulcer areas, reduction of edema and leucocytes infiltration of the submucosal layer.  相似文献   

15.
研究了雄黄对大鼠脑组织氨基酸类神经递质含量的影响.将32只Wistar大鼠随机分为对照组(0.5%CMC-Na)以及低剂量(0.3g/kg)、中剂量(0.9g/kg)、高剂量(2.7g/kg)雄黄染毒组,通过连续灌胃给予雄黄混悬液两周.采用高效液相色谱-柱前衍生化法测定了大鼠脑组织中氨基酸类神经递质含量的变化.结果表明,与对照组比较,低剂量组大鼠脑组织中丝氨酸、甘氨酸和γ-氨基丁酸含量明显增加.中、高剂量组大鼠脑组织中同型半胱氨酸、谷氨酰胺、丝氨酸和天冬氨酸含量明显比对照组的低.总体而言,雄黄可对大鼠脑组织氨基酸类神经递质产生影响,氨基酸类神经递质可能是雄黄毒性作用的靶点之一.  相似文献   

16.
Forchlorfenuron (CPPU) is a plant growth regulator extensively used in agriculture. However, studies on CPPU pharmacokinetics are lacking. We established and validated a rapid, sensitive, and accurate liquid chromatography–mass spectrometry method for CPPU detection in rat plasma. CPPU pharmacokinetics was evaluated in adult and juvenile rats orally treated with 10, 30, and 90 mg/kg of the compound. The area under the plasma drug concentration–time curve from 0 to 24 h (AUC), at the final time point sampled (AUC0–t), and the maximum drug concentration of CPPU increased in a dose-dependent manner. The pharmacokinetic parameters AUC0–t and absolute bioavailability were higher in the juvenile rats than in adult rats. The mean residence time and AUC0–t of juvenile rats in the gavage groups, except for the 10 mg/kg dose, were significantly higher in comparison to those observed for adult rats (p < 0.001). The plasma clearance of CPPU in juvenile rats was slightly lower than that in the adult rats. Taken together, juvenile rats were more sensitive to CPPU than adult rats, which indicates potential safety risks of CPPU in minors.  相似文献   

17.
The aim of the present study was to investigate the anticancer and immunity activity of β-carotene in hepatocellular carcinoma (HCC) rats. Three days after transplantation, forty Wistar rats were randomly divided into four groups, each group consisting of 10 animals. These groups were control group (untreated), low-dose β-carotene-treated group (20 mg/kg), middle-dose group (40 mg/kg) and high-dose (60 mg/kg) group. β-Carotene-treated groups were fed with β-carotene (20, 40, 60 mg/kg b.w.) orally for 30 days. Control group was treated with the same volume of physiological saline. Another ten rats were served as the normal group. Results showed that 30 days of β-carotene treatment could significantly inhibit tumour growth, enhance blood NK, IL-2, TNF-α, WBC, TP, ALB and A/G levels, and decrease blood ALT, AST and ALP activities in HCC rats. Pathological analysis of liver tissue showed that β-carotene treatment may decrease damage of liver tissue in HCC rats. It can be concluded that β-carotene may improve the immunity function and inhibit tumour growth in HCC rats.  相似文献   

18.
将32只Wistar大鼠随机分为对照组(口服0.5%羧甲基纤维素钠溶液)以及低剂量(0.3g/kg)、中剂量(0.9g/kg)和高剂量(2.7g/kg)雄黄混悬液处理组,通过6周连续灌胃给服雄黄混悬液,采用高效液相色谱法测定大鼠脑组织中三磷酸腺甙(ATP)的含量,研究了雄黄对大鼠脑组织能量代谢的影响.结果表明,与对照组比较,雄黄染毒组大鼠脑组织中ATP含量均呈下降趋势(P<0.05),不同剂量组间未表现明显差异(P>0.05).这表明雄黄对大鼠脑组织能量代谢具有一定的抑制作用.  相似文献   

19.
研究了朱砂对大鼠脑组织中氨基酸类神经递质含量的影响.将32只Wistar大鼠随机分为低、中、高剂量组和对照组,朱砂灌胃给药14天后,采用高效液相色谱法测定大鼠脑组织中谷氨酸(Glu)、天门冬氨酸(Asp)、甘氨酸(Gly)、γ-氨基丁酸(GABA)和牛磺酸(Tau)的含量,并计算兴奋毒性指数(EI)的变化.与对照组相比较,脑组织中氨基酸类神经递质含量均呈下降趋势,其中Asp和Gly的中、高剂量组差异有统计学意义(P0.05),Tau和GABA的高剂量组有统计学差异(P0.05),Glu和EI所有剂量组均有统计学差异(P0.05).朱砂对氨基酸类神经递质具有一定的抑制作用.  相似文献   

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