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1.
大豆黄酮对去卵巢猪LH分泌的影响   总被引:6,自引:0,他引:6  
去卵巢的德国格丁根微型小母猪、于静脉内注射或皮下埋植大豆黄酮,并以雌激素诱导后,观察其对垂体LH反馈性分泌的影响。试验分两系列。第一系列共三组,每组6头:试验组按每10μg/kg体重静脉注入大豆黄酮悬浮液,对照Ⅰ组注入相等量大豆黄酮溶剂,对照Ⅱ组作空白对照。第二系列为二组,每组9头动物,试验组皮下埋植大豆黄酮硅胶囊,对照组埋植不含任何药品的硅胶管,埋植期12天。埋植后第7天,两组同时肌注雌二醇。慢性血管导管采集血样,RIA分析血浆LH。结果表明,系列试验一,试验组注射大豆黄酮后LH分泌呈下降趋势,LH平均水平和峰值在处理后第1小时明显低于对照组,尔后与对照组趋于相似。系列试验二,试验组在大豆黄酮埋植后第4天和第7天,LH平均水平明显低于对照组和自身埋植前。雌激素处理后48h内,试验组LH分泌几乎完全被抑制,而对照组仍有明显分泌(P<0.001)。LH正反馈峰,试验组较对照组晚12h出现,但峰值显著高于对照组。结果表明,大豆黄酮对去卵巢猪垂体LH分泌具有类雌激素效应,而其程度可能与大豆黄酮处理剂量和处理时间有关。  相似文献   

2.
目的观察不同子宫、卵巢切除术式对兔术后早期内分泌激素和骨代谢的影响。方法45只健康成年雌兔随机分为5组,Ⅰ组:单纯子宫全切除组;Ⅱ组:子宫全切+单侧卵巢切除组;Ⅲ组:子宫全切+双侧卵巢切除组;Ⅳ组:双侧卵巢切除组;Ⅴ组:对照组。测量术前、术后1、2、3个月的体重、雌二醇(E2)、甲状旁腺素(PTH)、血钙、血清碱性磷酸酶(ALK)和骨密度(BD)。结果术后第2、3个月,Ⅲ组、Ⅳ组出现烦躁不安和体重减轻的实验兔要显著高于Ⅰ组和Ⅱ组;术后第2个月,Ⅱ组E2浓度(17.66±6.06)pg/mL,显著降低,术后第3个月,血钙增高(3.86±0.11)mmol/L,第2椎骨骨密度显著降低,与对照组相比(P〈0.05),有显著差异;Ⅱ组术后第3个月PTH增高,但与对照组相比无显著差异(P〉0.05)。Ⅲ组、Ⅳ组术后第2个月起,E2、PTH、血钙、ALT和BD,与对照组相比均有显著改变。结论子宫切除术会影响雌兔内分泌的变化,只保留单侧卵巢时不能维持相应的正常生理功能。  相似文献   

3.
维生素C和E混合饲喂对中华鳖幼鳖抗酸应激能力的影响   总被引:8,自引:0,他引:8  
来自甲鱼养殖场的60只中华鳖(Pelodiscus sinensis)幼鳖驯养3周后,实验设5组:对照组、处理Ⅰ、Ⅱ、Ⅲ和Ⅳ组。各组设2个平行,依次在饵料中混合添加维生素C(Vc)和E(VE)为0和0、250和50、2500和50、250和250、2500和250mg/kg,喂食4周后,每组取半数幼鳖经酸应激处理24h。取幼鳖血液,用镜检法测定血细胞的吞噬率,透射比浊法测定血清溶菌活力、杀菌活力以及补体C3和C4含量。①经酸应激与未经酸应激处理相比:对照组血细胞吞噬率显著降低,而处理Ⅰ-Ⅳ组无显著变化;对照组和处理Ⅰ组血清溶菌活力和补体C3含量显著下降,而处理Ⅱ-Ⅳ组无显著变化;血清杀菌活力均有显著下降(对照组、处理Ⅰ和Ⅲ组极显著,处理Ⅱ组和Ⅳ组显著);对照组、处理Ⅰ和Ⅲ组血清补体C4显著下降,而处理Ⅱ和Ⅴ组无显著变化。②经酸应激处理,血细胞吞噬率、血清溶菌活力、杀菌活力和补体C3含量,处理Ⅰ~Ⅳ组的均显著高于对照组,处理Ⅳ组显著高于其他4组;血清杀菌活力,处理Ⅱ组又高于处理Ⅰ和Ⅲ组;血清补体C4,对照组显著低于处理Ⅰ-Ⅳ组,而处理Ⅰ-Ⅳ组间无显著相异。Vc和VE混合饲喂对酸应激后中华鳖血细胞吞噬率、血清溶菌活力、杀菌活力和补体C3含量有显著协同促进作用,对血清补体C4的合成无协同作用。说明Vc和VE混合饲喂能显著增强中华鳖抗酸应激能力,缓解或部分缓解酸应激造成的不利影响。  相似文献   

4.
目的探讨苏丹红对小白鼠血液和组织器官的影响。方法取小鼠连续12 d腹腔注射不同剂量苏丹红Ⅰ、Ⅱ、Ⅲ、Ⅳ(0、40、80、160 mg/kg),末次给药24 h后采集血样,用血细胞分析仪检测血常规指标,毛细血管法测定凝血时间,剖腹取主要器官称重,计算脏器系数。结果苏丹红Ⅰ和Ⅱ组血液红细胞数明显减少,而苏丹红Ⅲ和Ⅳ组不明显,苏丹红不同剂量之间比较,低剂量苏丹红Ⅰ和高剂量苏丹红Ⅱ组比苏丹红Ⅲ和Ⅳ组血液红细胞数变化明显;苏丹红Ⅰ和Ⅱ组血液血红蛋白含量明显降低,而苏丹红Ⅲ和Ⅳ组血红蛋白含量变化不明显。四种不同剂量苏丹红组小鼠血液中血小板数量减少,随着剂量增加小鼠血液凝固时间延长。随着苏丹红剂量增加,苏丹红I和II组小鼠血液白细胞数比对照组明显增加,苏丹红Ⅲ和Ⅳ组白细胞数有增加趋势但差异不显著。与对照组比较,苏丹红组小鼠血液白细胞数明显增加、而淋巴细胞和单核细胞显著减少。随着苏丹红注射剂量增加,肾脏和脾脏脏器系数较对照组明显增大,肝脏脏器系数变化不明显。结论苏丹红对小鼠血液细胞、血红蛋白、血小板和凝血时间以及组织器官都有不同程度影响。  相似文献   

5.
旨在研究饲料中添加不同比例的韭菜对种蛋孵化的影响。在相同饲养条件下,选取4周龄的海兰褐种公鸡400只,随机分为4组,每组5个重复,每个重复20只。Ⅰ组是对照组,喂基础饲料;Ⅱ组、Ⅲ组、Ⅳ组分别在基础饲料中添加1%、3%、5%的韭菜,饲喂16周,第20周龄结束后,进行人工授精。授精后第4d,每组随机抽取500枚种蛋进行孵化。其中A组为对照组Ⅰ的种蛋,B、C、D组分别是试验组Ⅱ、Ⅲ、Ⅳ组的种蛋。结果显示:饲料中添加适量韭菜可以显著提高种蛋的孵化率、健雏率和平均初生重(P0.05)。本研究说明了饲料中添加韭菜可提高种蛋的孵化率、健雏率和平均初生重,且添加5%韭菜孵化效果最理想。  相似文献   

6.
为探讨维生素C (VC)和维生素E (VE)联用对应激和非应激中华鳖幼鳖的生长、肝脏VC 和VE 以及血清皮质醇含量的影响 ,作者使用了 5组饵料 ,VC 和VE 的添加量依次为 0和 0mg/kg (对照组 )、 2 5 0和 5 0mg/kg (实验Ⅰ组 )、2 5 0 0和 5 0mg/kg (实验Ⅱ组 ) ;2 5 0和 2 5 0mg/kg (实验Ⅲ组 ) ;2 5 0 0和 2 5 0mg/kg(实验Ⅳ组 )。中华鳖幼鳖的生长、肝脏VC 和VE以及血清皮质醇分别通过特定生长率、高压液相色谱法和放免法来测定。结果实验Ⅰ -Ⅳ组中华鳖的特定生长率明显高于不加VC 和VE的对照组 ,但实验Ⅰ -Ⅳ组间没有明显不同。非应激中华鳖肝脏VC 和VE的含量随饵料中VC 和VE 含量的增加而明显升高 ,并且实验Ⅱ -Ⅳ组肝脏VC 和VE都明显高于对照组和实验Ⅰ组。酸应激后 ,对照组和实验组中华鳖肝脏VC 和VE都有下降的趋势 ,但无显著差异 ;应激后实验Ⅱ -Ⅳ组肝脏VC 和VE均明显高于对照组 ,实验Ⅳ组明显高于其它 4组。血清皮质醇的含量在实验Ⅰ -Ⅳ组间没有明显不同 ,实验Ⅰ -Ⅲ组与对照组相比虽有降低的趋势但没有变化 ,实验Ⅳ组则明显低于对照组。酸应激后 ,对照组血清皮质醇明显升高 ,其他 4组虽有升高的趋势 ,但没有明显变化。应激后实验Ⅰ -Ⅳ组血清皮质醇的含量均明显低于对照组 ,实验Ⅰ -Ⅳ组间没有明显  相似文献   

7.
目的探讨纳豆芽胞杆菌作为饲料添加剂对AA肉鸡生产性能和免疫功能的影响。方法将300只1日龄的AA健康肉鸡,随机分为5组,对照组饲喂基础日粮,实验组在基础日粮中分别添加50、100、150和200mg/kg纳豆芽胞杆菌(处理组Ⅰ~Ⅳ),检测其对AA肉鸡增重、饲料转化率、新城疫疫苗免疫后的抗体水平和免疫器官指数的影响。结果在21d时,处理4个组肉鸡的体重分别较对照组高0.23%、6.16%、8.29%和7.82%,其中处理组Ⅱ、Ⅲ与对照组相比差异有统计学意义(P0.05);处理组Ⅰ、Ⅳ与对照组相比差异无统计学意义(P0.05);在7~28d时处理4个组肉鸡的饲料转化率均稍高于对照组,但差异无统计学意义(P0.05);当21d时,处理组Ⅱ、Ⅲ的效价水平与对照组、处理组Ⅰ及Ⅳ相比差异有统计学意义(P0.05)。处理组Ⅰ~Ⅳ的胸腺、脾脏以及法氏囊三项指数均显著优于对照组,尤其是处理组Ⅱ和Ⅲ的免疫器官指数提升最为显著(P0.05)。结论在AA肉鸡基础日粮中添加100、150mg/kg的纳豆芽胞杆菌对于其生产性能的改善和免疫功能的提高有显著效果。  相似文献   

8.
本实验用硫酸腺嘌呤预处理方法与经典缺血预处理方法对比分析大鼠心肌酶活性及SDH的电镜细胞化学结构。雄性SD大鼠24只,分4组,即Ⅰ组:正常对照组,Ⅱ组:缺血再灌注组;Ⅲ组:经典缺血预处理组;Ⅳ组:硫酸腺嘌呤预处理组。检测肌酸激酶(CK)、细胞色素氧化酶(CCO)及琥珀酸脱氢酶(SDH)的活性。结果显示:与Ⅱ组比,Ⅲ组、Ⅳ组CK漏出减少,CCO、SDH活性增强,细胞超微结构保存良好。结果表明:硫酸腺嘌呤预处理方法具有类似经典缺血预处理效应。  相似文献   

9.
检测暴露于手机辐射下的孕鼠及其子代的细胞免疫因子含量水平,以探讨手机电磁辐射对孕鼠及其子代免疫功能的影响,为孕妇科学、合理使用移动通信工具提供参考。30只孕鼠随机分为Ⅰ、Ⅱ、Ⅲ、Ⅳ、Ⅴ组,每组6只,对应为空白对照组、待机对照组1、0min低强度组、30min中强度组和60min高强度组。ELISA检测孕鼠分娩24h内孕鼠及新生乳鼠外周血中IFN-γ和IL-4的含量。对Ⅰ、Ⅱ、Ⅲ、Ⅳ、Ⅴ各组母鼠外周血中IFN-γI、L-4含量进行比较,其差异无统计学意义(P>0.05);Ⅳ、Ⅴ组新生小鼠外周血中IFN-γI、L-4含量与Ⅰ、Ⅱ组比较,其差异有统计学意义(P<0.05),而且Ⅴ组新生小鼠外周血中IFN-γI、L-4含量与Ⅲ组比较,其差异也具有统计学意义(P<0.05)。手机辐射降低了胚胎期小鼠的IFN-γ和IL-4含量。  相似文献   

10.
目的:探讨血清异常凝血酶原(PIVKA-Ⅱ)、钙网膜蛋白(Calretinin)及DJ-1蛋白在卵巢癌中的表达及与病情严重程度的相关性。方法:选择2019年3月至2020年3月我院接诊的100例卵巢癌患者为本研究对象,设为病例组,并选择我院同期体检的健康对照组90例,分析两组血清PIVKA-Ⅱ、Calretinin及DJ-1蛋白水平的表达,及其与卵巢癌患者病情严重程度的相关性。结果:病例组血清PIVKA-Ⅱ、Calretinin及DJ-1蛋白水平显著高于对照组,差异显著(P<0.05);Ⅰ~Ⅱ期组患者血清PIVKA-Ⅱ、Calretinin及DJ-1蛋白水平显著低于Ⅲ期、Ⅳ期患者,Ⅲ期患者血清PIVKA-Ⅱ、Calretinin及DJ-1蛋白水平显著高于Ⅳ期患者,差异显著(P<0.05);相关性分析结果中显示,血清PIVKA-Ⅱ、Calretinin及DJ-1蛋白和病理分期之间呈正相关(P<0.05)。结论:在卵巢癌患者中血清PIVKA-Ⅱ、Calretinin及DJ-1蛋白与病情严重程度之间存在着密切关系,可作为卵巢癌的潜在标记物。  相似文献   

11.
Daidzein is a potential natural alternative to estradiol during therapy of some malignancies in men. Besides weak inhibition of tyrosine kinase activity, daidzein has a sizeable inhibitory effect on calcium channels. The aim of this study was to examine the effects of daidzein on the immunohistomorphometric features of pituitary adrenocorticotropes (ACTH cells) and circulating levels of ACTH and corticosterone, in comparison with estradiol, in an animal model of the andropause. Sixteen-month-old Wistar rats were divided into sham operated (SO), orchidectomized (Orx), estradiol treated orchidectomized (Orx+E) and daidzein treated orchidectomized (Orx+D) groups. Estradiol (0.625 mg/kg/day) and daidzein (30 mg/kg/day) were administered subcutaneously for three weeks, while the SO and Orx groups received the vehicle alone. ACTH cells were identified by the peroxidase-antiperoxidase (PAP) immunohistochemical procedure. Peripheral circulating concentrations of ACTH and corticosterone were measured by immunoassay. Orchidectomy reduced (p<0.05) the cell volume and volume density of adrenocorticotropes by 11% and 16%, respectively, in comparison to SO rats. In Orx+E rats, the volume density of ACTH cells decreased (p<0.05) by 25%, but the circulating level of ACTH increased (p<0.05) by 29%, compared to Orx rats. Daidzein treatment significantly decreased (p<0.05): volume density of ACTH cells, circulating ACTH and corticosterone by 24%, 48% and 33%, respectively, compared to the Orx group. In conclusion, this study revealed that daidzein negatively modulated the immunohistomorphometric features of ACTH cells and, unlike estradiol, decreased ACTH and corticosterone secretion, in an animal model of the andropause.  相似文献   

12.
We compared the effects of two major isoflavones, daidzein and genistein, on lipid metabolism in rats. Daidzein (150 mg/kg diet), genistein (150 mg/kg diet), daidzein and genistein (1:1, 300 mg/kg diet), or control diets were fed to 4 groups of 6-week-old ovariectomized (Ovx) and non-Ovx Sprague Dawley rats for 4 weeks. Dietary daidzein, but not genistein, reduced serum and hepatic total cholesterol levels significantly relative to that by the control group, regardless of whether the rats had undergone ovariectomy. Genistein did not exhibit any physiological effects on lipid levels, but did affect genes involved in cholesterol metabolism. These results indicate that daidzein and genistein may influence lipid regulation via differing modes of action.  相似文献   

13.
Daidzein (4',7-dihydroxyisoflavone), a soy phytoestrogen, is a weakly estrogenic compound that may have potential health benefits. Biotransformation of daidzein by the human gut microflora after ingestion converts it to either the highly estrogenic metabolite equol or to nonestrogenic metabolites. We investigated the metabolism of daidzein by colonic microflora of rats. Fecal samples, obtained before and after rats were exposed to daidzein at 250 or 1000 parts per million, were incubated in brain-heart infusion (BHI) broth with daidzein under anaerobic conditions. Samples were removed from the cultures daily and analyzed by high-performance liquid chromatography (HPLC) and mass spectrometry. The fecal bacteria of all rats, regardless of prior daidzein exposure, metabolized the added daidzein to dihydrodaidzein. Both compounds disappeared rapidly from BHI cultures incubated for more than 24 h, but no other daidzein metabolites were detected. Only daidzein and dihydrodaidzein were found in a direct analysis of the feces of rats that had consumed daidzein in their diets. Unlike the fecal bacteria of humans and monkeys, the rat flora rapidly metabolized daidzein to aliphatic compounds that could not be detected by HPLC or mass spectral analysis.  相似文献   

14.
36只烫伤大鼠,分为纳洛酮组和盐水对照组。两组动物侧脑室分别注射纳洛酮和生理盐水,观察纳洛酮对烫伤休克的影响。 结果表明:纳洛酮组大鼠的存活率高于盐水对照组。纳洛酮组动物烫伤后2小时存活率为83%,烫伤后4小时存活率为39%;盐水组动物烫伤后2小时存活率为44%,烫伤后4小时存活率为5.6%。纳洛酮组血压下降和心率减慢的进度也较慢,烫伤后180分钟血压才降低到63%,而盐水组在烫伤后90分钟血压已降低到62%。纳洛酮组动物的呼吸和体温变化也较慢。这些结果提示:纳洛酮具有一定的抗烫伤休克的作用。  相似文献   

15.
Suppression of food intake and body weight gain by naloxone in rats   总被引:1,自引:0,他引:1  
The effect of acute and chronic administration of naloxone on food acquisition and weight gain in rats was studied in 3 experiments. One injection of a sparingly-soluble salt of naloxone in slow-release vehicle markedly lowered mean food intake over that of control rats injected with the vehicle only. Mean body weight of the naloxone-injected rats was significantly lower than that of the control group for one week.Repeated evening injections (2000 h) of naloxone hydrochloride in saline tended to reduce the night-time feeding below control levels throughout the 10-day period of naloxone administration. Food intake was significantly lower in the 4- and 8-h periods after the first injection of naloxone than that on the preceding saline control night. The initial decreases were offset by increased day-time feeding so that total daily food intake was not significantly altered over the 10 days. When saline was substituted for naloxone, food intake increased.Rats given naloxone following 24 h of fasting consumed significantly less food and gained less weight during 4 h of access to food compared to those receiving saline. After a 48-h fast naloxone-treated rats also gained significantly less body weight than those given saline, but the reduction in food intake was not statistically significant. These results suggest the possibility that endorphins may have a modulating effect on feeding activity.  相似文献   

16.
Isoflavones are biologically active plant derived compounds that have several health promoting effects. In the present study hitherto unknown effects of one of the well known isoflavonoids, daidzein, has been evaluated on its chemo-preventive action against breast cancers in pre-pubertal rats. Either daidzein (500 μg/g bwt) or vehicle, dimethyl sulphoxide (DMSO), was administered at 16th, 18th, and 20th day post-partum and the chemopreventive efficacy was evaluated in dimethylbenz[a]nthracene (DMBA) induced Sprague-Dawley rats, at 50th day. To elucidate the mechanism of action, the antioxidative status was also examined in the liver and mammary gland of prebubertal rats using two different doses of daidzein (0.5 mg/kg bwt and 50 mg/kg bwt, p.o.) for 10 days. The specific activity of antioxidant enzymes as well as reduced glutathione (GSH) level and peroxidative damage were evaluated spectrophotometrically, both in liver as well as in mammary gland. Animals treated with daidzein pre-pubertally, showed a significant reduction in the tumorigenesis of mammary gland up to 37.4% as compared to animals induced for tumors with DMBA. In animals treated with 50 mg/kg of daidzein, a significant increase in the specific activities of the antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione transferase (GST), DT-diaphorase (DTD), and in GSH content were observed in both liver and mammary gland. Expectedly, the specific activity of lactate dehydrogenase (LDH) and level of peroxidative damage was decreased, as compared to that of control group of animals. Our results suggest that, daidzein can be considered as a potent chemopreventive agent against mammary carcinogenesis in pre-pubertal animals, with modulation of antioxidant enzymes being one of its mechanisms of actions.  相似文献   

17.
Current evidence suggests that endogenous opioid peptides (EOPs) tonically inhibit secretion of luteinizing hormone (LH) by modulating the release of gonadotropin-releasing hormone (GnRH). Because of their apparent inhibitory actions, EOPs have been assumed to alter both pulse frequency and amplitude of LH in the rat; and it has been hypothesized that EOP pathways mediate the negative feedback actions of steroids on secretion of GnRH. In order to better delineate the role of EOPs in regulating secretion of LH in the male rat, we assessed the effects of a sustained blockade of opiate receptors by naloxone on pulsatile LH release in four groups: intact male rats, acutely castrated male rats implanted for 20 h with a 30-mm capsule made from Silastic and filled with testosterone, acutely castrated male rats implanted for 20 h with an osmotic minipump dispensing 10 mg morphine/24 h, and male rats castrated approximately 20 h before treatment with naloxone. We hypothesized that if EOPs tonically inhibited pulsatile LH secretion, a sustained blockade of opiate receptors should result in a sustained increase in LH release. We found that treatment with naloxone resulted in an immediate but transient increase in LH levels in intact males compared to controls treated with saline. Even though mean levels of LH increased from 0.15 +/- 0.04 to a high of 0.57 +/- 0.14 ng/ml, no significant difference was observed between the groups in either frequency or amplitude of LH pulses across the 4-h treatment period. The transient increase in LH did result in a 3- to 4-fold elevation in levels of plasma testosterone over baseline. This increase in testosterone appeared to correspond with the waning of the LH response to naloxone. The LH response to naloxone was eliminated in acutely castrated rats implanted with testosterone. Likewise, acutely castrated rats treated with morphine also failed to respond to naloxone with an increase in LH. These observations suggest that chronic morphine and chronic testosterone may act through the same mechanism to modulate secretion of LH, or once shut down, the GnRH pulse-generating system becomes refractory to stimulation by naloxone. In acutely castrated male rats, levels of LH were significantly increased above baseline throughout the period of naloxone treatment; this finding supports the hypothesis that the acute elevation in testosterone acting through mechanism independent of opioid is responsible for the transient response of LH to naloxone in the intact rat.  相似文献   

18.
This study compared the ability of daidzein, a soy isoflavone, with that of 17beta-estradiol to prevent bone loss in cadmium (Cd)-exposed ovariectomized (OVX) rats during growth. Four week-old female Wistar rats were randomly assigned to five treatment groups of 9 rats each, either (1) sham-operated (SH); (2) OVX and placed on experimental diets (OVX); (3) OVX fed 50 ppm of CdCl2 (OVX-Cd); (4) OVX fed 50 ppm of CdCl2 and 10 microg of daidzein per kg of body mass (OVX-CD-D); or (5) OVX fed 50 ppm of CdCl2 and 10 microg of estrogen per kg of body mass (OVX-CD-E). All rats were given free access to AIN-76 modified diet and drinking water, with or without Cd, for 8 weeks. The OVX groups gained more (P < 0.05) body mass than the SH group. Femoral mass was increased by feeding daidzein and estradiol, whereas femoral length was not (P > 0.05) significantly different among groups. Femoral breaking force was not significantly different among groups, however, femoral BMD was significantly lower in OVX-Cd than in the SH and OVX groups. Morphologically proliferative cartilage and hypertrophic cells in femur showed normal distribution in OVX-Cd-D and OVX-Cd-E groups unlike those in OVX-Cd group. These findings suggest that Cd-OVX-induced osteopenia or osteoporosis probably results from an increase in bone turnover.  相似文献   

19.
The effect of naloxone upon neurologic deficit was evaluated in a model of transient forebrain ischemia in rats. Awake male Wistar rats were subjected to a 30 minute ischemia by occluding both common carotid arteries 8 days after cauterizing vertebral arteries. Administration of naloxone 1 or 5 mg/kg iv 10 minutes after carotid occlusion or 1 mg/kg iv one hour after clamp removal failed to reduce immediate and tardive neurologic postischemic deficits. On the other hand, in rats treated by a dose of 1 mg/kg naloxone 10 minutes after carotid occlusion and perfused with an additional dose of 2 mg/kg/h for 80 minutes, neurologic score was improved one hour after ischemia. However mortality was not decreased whatever was the modality of naloxone administration. This result confirms previous data showing that naloxone exerts a protective effect when given at sufficiently high dosage.  相似文献   

20.
目的:研究硫酸软骨素时慢性酒精中毒氧化损伤的保护作用.方法:60只Wistar大鼠随机分成六个组:空白组给予蒸馏水,酒精模型组给予50%的酒精8 ml·kg-1·d-1灌胃,纳洛酮组在给予酒精三十分钟后腹腔注射纳洛酮0.08mgkg-1·d-1,硫酸软骨素低、中、高剂量组在酒精模型组的基础上分别给予硫酸软骨素50,100和150mg·kg-1·d-1.两周后酒精的剂量增加到12mg·kg-1d-1.在第八周末,分离大鼠脑组织,观察大鼠神经细胞.用生物方法测定大鼠脑组织中GSH-PX、SOD、MDA以及Ache的活性.结果:模型组大鼠大脑皮质和海马区神经细胞的数量明显减少并且排列紊乱;和酒精模型组相比较,硫酸软骨素中剂量组大脑皮质和海马区神经细胞排列较整齐,酒精+Chondroitin组脑组织中MDA的含量和Ache降低(P<0.01),GSH-PX的含量和SOD的活力均明显增加(P<0.01).结论:硫酸软骨素时慢性酒精中毒氧化损伤具有保护作用.  相似文献   

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