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1.
在水温(28±2)℃、盐度28条件下,将盐酸氯苯胍(Robenidine hydrochloride,ROBH)按30 mg/kg的剂量口灌红笛鲷(Luthjanus sanguineus),用HPLC-MS/MS法研究ROBH在红笛鲷体内的药代动力学和残留消除规律。结果表明:单剂量口灌给药后,红笛鲷血浆中ROBH的药时数据符合一级吸收二室模型,药物在血浆中的达峰时间t_p为1.79 h,血药浓度峰值C_(max)为211.38μg/L,药时曲线下面积(AUC_(0-∞))为5 229.16μg/(L·h),消除半衰期(t1/2β)为46.99 h。ROBH在红笛鲷其他组织中分布较广,消除速度较慢,肌肉、肝脏和肾脏的C_(max)分别为37.58、863.02、1 063.24μg/kg,t_p均为1.5 h,AUC0-∞分别1 017.03、20 841.20、30 743.04μg/(kg·h);t1/2β分别为26.35、14.05和24.31 h。连续5 d口灌给药后,红笛鲷血浆、肌肉、肝脏和肾脏中的药物消除半衰期t1/2分别为46.14、36.11、28.62、26.92 h。以10μg/kg为最高残留限量,肌肉作为食用靶组织,在本试验条件下,建议休药期不少于7 d。  相似文献   

2.
在水温(20±2)℃条件下,以10 mg/kg的剂量对健康眼斑拟石首鱼(Sciaenops ocellatus)腹注和口灌甲砜霉素,采用HPLC-MS/MS方法测定组织中的药物浓度,研究甲砜霉素在该鱼种体内的代谢动力学。结果显示,两种给药方式下眼斑拟石首鱼血浆药时数据均符合一级吸收二室模型;腹注给药后血浆、肾脏、肝脏和肌肉的药物峰值(C_(max))分别为5.50μg/m L、10.96μg/g、6.61μg/g和3.50μg/g,达峰时间(tp)分别为1.2、1.5、2.0和6.0 h,消除半衰期(t1/2β)分别为44.82、17.27、29.39和26.99 h;口灌给药后血浆、肾脏、肝脏和肌肉的Cmax分别为4.62μg/m L、7.11μg/g、4.99μg/g和3.58μg/g,tp分别为2.4、4.0、4.0和4.0 h,t1/2β分别为14.67、27.34、37.68和32.65 h。腹注给药方式下甲砜霉素在眼斑拟石首鱼体内的吸收快于口灌给药,在肾脏、肝脏和和肌肉中的消除快于口灌给药,在血浆中的消除则慢于口灌给药。  相似文献   

3.
在水温20±2℃的条件下,按10 mg/kg的剂量通过腹腔注射和口灌方式,以液-质联用法研究氟苯尼考在美国红鱼(Sciaenops ocellatus)体内的药代动力学和组织分布,所得药时数据用DAS3.0软件分析。结果显示,美国红鱼腹注氟苯尼考后血药经时符合一级吸收二室模型,而口灌氟苯尼考则符合一级吸收一室模型;腹腔注射组,美国红鱼血浆、肝脏、肾脏、肌肉的氟苯尼考出峰时间(tp)分别为0.5、4、0.5、4 h,峰浓度(ρmax)分别为15.47、9.90、6.83、2.73μg/g,药时曲线下面积(AUC)分别为394.10、105.66、157.37、120.01 mg/(L·h),消除半衰期分别为45.39、7.42、148.25、39.22 h;口灌组,美国红鱼血浆、肝脏、肾脏、肌肉的氟苯尼考出峰时间(tp)分别为2、1.5、4、4 h,峰浓度(ρmax)分别为6.31、5.44、9.10、5.12μg/g,药时曲线下面积(AUC)分别为136.21、162.32、213.32、157.37 mg/(L·h),消除半衰期t1/2β分别为12.08、27.9、14.85、38.53 h。结果表明,氟苯尼考注射给药在美国红鱼体内的吸收快于口灌给药,腹注给药氟苯尼考除在肝脏中的消除快于口灌给药外,在血浆、肌肉和肾脏中的消除均慢于口灌给药。  相似文献   

4.
在水温26±2℃、盐度28条件下,恩诺沙星(enrofloxacin,EF)按5 mg/kg的剂量腹腔注射和口灌红笛鲷(Lutjanus sanguineus),用反相高效液相色谱法研究恩诺沙星在红笛鲷体内的药代动力学和组织分布。结果显示:注射和口灌后红笛鲷血浆的药时数据均符合一级吸收二室模型;血药达峰时间(tp)分别为0.75和1.5 h,血药质量浓度峰值(cmax)分别为5.22和3.94μg/mL,药时曲线下面积(AUC)分别36.98和17.24 mg/(L.h),消除半衰期(t1/2β)分别为13.28和9.18 h;恩诺沙星在组织中分布较广,注射和灌服给药肌肉、肝脏和肾脏的cmax分别为3.53和3.40μg/g、4.08和3.98μg/g、11.23和5.40μg/g,tp分别为1.5和2.0 h、1.0和2.0 h、0.75和1.5 h,AUC分别33.17和23.12 mg/(L.h)、39.36和18.20 mg/(L.h)、98.97和56.69 mg/(L.h);EF在红笛鲷体内消除速度较慢,注射和灌服给药肌肉、肝脏和肾脏的t1/2β分别为22.08和83.32 h、41.52和94.47 h、20.94和21.81 h。表明恩诺沙星注射给药在红笛鲷体内的吸收和消除均快于口灌给药。  相似文献   

5.
【目的】研究凡纳滨对虾(Litopenaeusvannamei)中丁香酚的残留和消除规律,保障水产品丁香酚麻醉运输安全。【方法】通过低浓度长时(50 mg/L 10 h)麻醉和高浓度短时麻醉(180 mg/L 8 min)两种不同麻醉方式对凡纳滨对虾进行药浴麻醉实验,采用气相色谱串联质谱法检测丁香酚的残留量。【结果】残留实验中,肌肉中丁香酚的残留量最高,虾头其次,肝胰腺中最低。采用低浓度长时麻醉凡纳滨对虾后,肌肉、虾头、肝胰腺中丁香酚残留量分别在1 h、8 h、1 h时达到最高峰,而高浓度短时麻醉的残留量始终低于低浓度长时间麻醉。消除实验中,肝胰腺中丁香酚的消除速率最快,肌肉其次,虾头中最慢。采用低浓度长时麻醉凡纳滨对虾,肝胰腺中丁香酚残留量在4 h内从药峰值Cmax 11.420μg/kg迅速消除,而虾头和肌肉在8 h内消除,最高峰Cmax分别为1.853μg/kg和11.610μg/kg。采用高浓度短时麻醉凡纳滨对虾并重复麻醉,肌肉和肝胰腺中的丁香酚含量从药峰值消除至0.800μg/kg需要4h,而虾头需要12h。【结论】残留实验中,低浓度长时麻醉凡纳滨对虾,残留量出现双峰现象,而后随着时间增加逐渐减少;高浓度短时麻醉凡纳滨对虾,丁香酚的残留在各组织中从最高残留量急剧下降。消除实验中,残留量随时间延长逐渐降低。在相应条件下建议丁香酚的休药期不少于48 h。  相似文献   

6.
在水温28℃条件下,以12 mg/kg剂量对罗非鱼单次口服给药,采用HPLC方法测定不同时间实验鱼肝脏和肾脏中的药物水平,分析氟苯尼考在罗非鱼肝、肾组织的吸收及消除规律。结果显示,肝脏和肾脏中的药动学参数均符合药动学一室模型,肝脏的药物消除速度快于肾脏,消除半衰期T1/2β分别为4.89 h和15.93 h;药物在肝脏的Tmax为5.43 h,吸收峰值为4.84μg/g;59 h后肝、肾组织中的药物含量均低于0.8μg/g。取12 mg/kg剂量连续给药7 d的实验鱼肝、肾组织,进行组织学观察,结果显示,给药组罗非鱼的肝、肾组织均未出现病理性变化。此外,氟苯尼考对6株罗非鱼常见病原菌的体外抑菌实验中,最小抑菌浓度(MIC)均≤4 mg/L,表明常用剂量氟苯尼考在罗非鱼体内消除快、残留少且不造成组织损伤,对常见病原菌具有良好的抑菌效果。  相似文献   

7.
为研究氨基酸螯合钴对凡纳滨对虾的营养效果,在凡纳滨对虾配合饲料中添加5、10、15 mg/kg的氯化钴和蛋氨酸钴。饲养8周,4周末(饲养中期)称重,8周末称重并采集对虾肝胰脏和肌肉,测定肝胰脏和肌肉中的钴含量。结果表明:钴的添加形式和钴水平不影响对虾0~4周增重率,15 mg/kg蛋氨酸钴显著提高了对虾0~8周增重率,且两种形式的钴之间差异显著(P<0.05)。51、0 mg/kg的蛋氨酸钴和5、101、5 mg/kg的氯化钴不影响8周末对虾的增重率。特定生长率、饲料系数和蛋白质效率的变化趋势与增重率类似。钴的添加形式和钴水平不影响肌肉中的钴含量,15 mg/kg的氯化钴组肝胰脏中钴含量显著高于对照组(P<0.05),其他各组间无显著差异;蛋氨酸钴各组肝胰脏中钴含量无显著差异;钴的添加形式不影响肝胰脏中钴含量。统计结果表明,促进生长方面,两种钴之间存在显著差异,蛋氨酸钴的营养效果好于氯化钴。饲料中蛋氨酸钴的添加量为15 mg/kg时,对虾生长最快,5 mg/kg时,可满足需要。  相似文献   

8.
研究0、300、600、900、1 200、1 500 mg/kg 6个L-肉碱添加水平对牙鲆(Paralichthys olivaceus)幼鱼生长、生化组成和血液指标的影响。结果表明:添加量为1 200 mg/kg的处理组牙鲆幼鱼的增重率和特定生长率显著提高,饲料系数显著降低(P<0.05);随着饲料中L-肉碱含量的增加,肝指数呈现下降趋势,且在添加量为900~1 500 mg/kg时,各组较对照组差异显著(P<0.05);饲料中添加L-肉碱显著降低各实验组脏体比(P<0.05),而对各处理组间存活率和肥满度均无影响(P<0.05);肌肉和肝脏中的脂肪含量与L-肉碱添加量呈负相关,当添加量为1 200~1 500 mg/kg时,较对照组差异显著(P<0.05);肌肉中的蛋白含量与L-肉碱添加量呈正相关,但各组差异不显著(P<0.05);饲料中添加L-肉碱降低血清中的谷草转氨酶、胆固醇、甘油三酯和尿素氮含量,且添加量1 200 mg/kg组各指标含量均显著低于对照组(P<0.05);各处理组的血糖含量较对照组均有所增加,其中1 200 mg/kg组血糖含量较对照组提高41.6%(P<0.05);血清中总蛋白和低密度脂蛋白均随着L-肉碱添加量的增加而呈下降趋势,高密度脂蛋白却得以提升,但差异均不显著(P<0.05)。分析认为,在本实验条件下,饲料中添加L-肉碱可促进牙鲆幼鱼生长,且降脂效果显著。建议L-肉碱最适添加量为1 200 mg/kg。  相似文献   

9.
Endocrine disrupting chemicals (EDCs) are increasingly viewed as persistent pollutants, similar to natural hormones in function. This paper describes the expression profiles of 7 genes (DMRT, VTG, GnRHR, FSHR, CYP17A, CYP19A, and CYP19B) involved in sex steroid synthesis and action as well as sexual development in adult male and female Cynoglossus semilaevis, after exposure to different concentrations of Bisphenol A (BPA) and 17β-estradiol (E2). Both BPA (1, 10, 50, 125, and 250 mg/kg) and E2 (0.5, 5, and 10 mg/kg) induced changes in target gene expression, although the estrogenic effects of E2 as a model estrogen were stronger. Among the 7 genes, VTG, CYP17A and CYP19 responded strongly to BPA or E2 exposure and can thus serve as reference biomarkers for estrogenic EDCs exposure in marine teleosts. These data will provide a window to establish a hypothalamic-pituitary-gonadal model in C. semilaevis to better understand the effect pathways of EDCs.  相似文献   

10.
在斜带石斑鱼(Epinephelus coioides)幼鱼基础饲料(铜质量分数2.03 mg/kg)中分别添加6个水平的羟基蛋氨酸螯合铜(hydroxy methionine copper,HMC),制成铜质量分数分别为2.03、4.04、6.20、10.67、13.96 mg/kg的实验饲料,饲喂6周后,探讨HMC对幼鱼生长、非特异性免疫酶活性和组织铜沉积的影响,确定幼鱼饲料中铜的最适需要量。结果表明,饲料中添加HMC,对石斑鱼的增重率、特定生长率(SGR)和饲料系数等生长性能的影响有统计学意义(P0.05),以铜质量分数6.20 mg/kg组增重率和特定生长率最高,饲料系数最低,高于或低于2.03和13.96 mg/kg组,差异有统计学意义(P0.05),与4.04和10.67 mg/kg组差异无统计学意义(P0.05);但对成活率、肝体比影响差异无统计学意义(P0.05)。饲料中添加HMC对全鱼水分和粗蛋白含量影响无统计学意义(P0.05),对全鱼粗灰分和粗脂肪含量影响有统计学意义(P0.05)。石斑鱼血浆铜蓝蛋白(CP)的含量、血清和肝脏总超氧化物歧化酶(T-SOD)及铜锌超氧化物歧化酶(Cu-Zn-SOD)活性均以6.20 mg/kg组最高;饲料中铜的添加对血清谷胱甘肽过氧化物酶(GSH-Px)活性和肝脏硫代巴比妥酸反应物(TBARS)含量影响无统计学意义(P0.05)。与对照组相比,饲料中添加HMC均提高鱼体、肌肉和肝脏中铜含量,差异有统计学意义(P0.05),且以13.96 mg/kg组最高。饲料中添加适量的HMC可提高石斑鱼幼鱼的生长性能,提高抗氧化能力。在本实验条件下,以SGR为判据,通过二次回归方程拟合可得,以HMC为铜源,斜带石斑鱼幼鱼铜需要量为7.09 mg/kg。  相似文献   

11.
We investigated the effect of tributyltin (TBT) exposure on the concentration of malondialdehyde (MDA) and the activity levels of the superoxide dismutase (SOD), catalase (CAT), and acid and alkaline phosphatase (ACP and AKP) enzymes in the small abalone, Haliotis diversicolor supertexta. We collected samples of the hepatopancreas and hemolymph 2, 6, 24, 48, 96, and 192 h after exposure to 0.35 μg (Sn)/L TBT. In the hepatopancreas, ACP activity was significantly higher in animals exposed to TBT 2, 24, and 96 h post-exposure compared with the control animals. AKP activity was also higher after 2 h, but SOD and CAT activity was unchanged. The concentration of MDA in the hemolymph was significantly higher than the control animals 2 and 6 h post-exposure. In the hemolymph of animals exposed to TBT, ACP activity was significantly lower than in the control animals 192 h post-exposure, whereas AKP activity was significantly lower 2 and 192 h post-exposure. Hemolymph SOD activity and levels of MDA were significantly lower than in the control animals 24 h after exposure but significantly higher after 96 h. Our results demonstrate that exposure to TBT cause rapid changes in ACP and AKP activity as well as altering the concentration of MDA in the hepatopancreas and hemolymph. SOD and CAT do not appear to be involved in the detoxification of TBT in the hepatopancreas of small abalone.  相似文献   

12.
Mercury (Hg) is one of the commonly encountered heavy metals, which is widespread in inshore sediments of China. In order to investigate the toxicity of Hg on marine invertebrates, we studied the effects of the divalent mercuricion (Hg2+) (at two final concentrations of 0.0025 and 0.0050 mg L−1, prepared with HgCl2) on metallothionein (MT) content, DNA integrity (DNA strand breaks) and catalase (CAT) in the gills and hepatopancreas, antioxidant enzyme activities of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx), in the hemolymph, gills and hepatopancreas of the portunid crab Charybdis japonica for an experiment period up to 15 d. The results indicated that MT was significantly induced after 3 d, with a positive correlation with Hg2+ dose and time in the hepatopancreas and a negative correlation with Hg2+ dose and time in the gills. While CAT in the hemolymph was not detected, it increased in the hepatopancreas during the entire experiment; SOD and GPx in the three tissues were stimulated after 12 h, both attained peak value and then reduced during the experimental period. Meanwhile, DNA strand breaks were all induced significantly after 12 h. These results suggested the detoxification strategies against Hg2+ in three tissues of C. japonica.  相似文献   

13.
Turbot Scophthalmus maximus, an important aquaculture species in China, currently suffers from epizootic diseases because of high density aquaculture. Enrofloxacin has been used to treat various systemic bacterial fish infections. However, studies concerning the pharmacokinetics of enrofloxacin in turbot are limited. In this study, the pharmacokinetics of enrofloxacin and its metabolite ciprofloxacin, were investigated in the turbot following intravenous and oral administration at 10 mg enrofloxacin/kg body weight, at 16°C and 10°C water temperatures. The concentrations of enrofloxacin and ciprofloxacin in the main tissues (plasma, muscle, liver and kidney) were detected by HPLC. The results show that the plasma concentration-time data for enrofloxacin were best described as a two-compartment open model after intravenous and oral administration. Three pharmacokinetic equations were established between the concentrations and temperatures. The kinetic profile of enrofloxacin was temperature dependent. The absorption half-life of enrofloxacin was 1.99 h and 2.17 h after oral administration, whereas the elimination half-life of the drug was 98.63 h and 136.59 h at 16°C and 10°C, respectively. The peak concentration of enrofloxacin in plasma and tissues was higher at 16°C than that at 10°C, and the peak plasma concentration time in the liver was the shortest at both temperatures among those of other tissues. The plasma C max /MIC ratio varied between 11.08 and 5 540.00 at 16°C; and between 7.92 and 3 960.00 at 10°C. The AUC/MIC ratio was 467.82-280 690.00 at 16°C, and 359.48-215 690.00 at 10°C. These ratios indicate that it is possible to obtain therapeutic efficacy. Very low levels of ciprofloxacin were detected. The AUC ratios of ciprofloxacin and enrofloxacin in plasma suggest that plasma ciprofloxacin might play a minor role in enrofloxacin treatment for turbot.  相似文献   

14.
This study investigated the effects of ammonia-N(control and 1 and 5 mg L~(-1)) on the changes of metabolic enzymes activities and nitrogenous compounds levels in the gills, hepatopancreas, muscles, and hemolymph of the swimming crab Portunus trituberculatus. Results showed that the levels of hemolymph ammonia increased significantly at 6 h and then decreased to control level at 12 h. The activities of key enzymes involved in biosynthesis pathways of glutamine(Gln) and urea, such as glutamate dehydrogenase(GDH), glutamine synthetase(GS), and arginase(ARG), increased remarkably in different tissues of P. trituberculatus. Gln level was the highest in muscles, while urea content was the largest in hepatopancreas. The m RNA expression level of xanthine dehydrogenase(XDH) was downregulated sharply in gills but upregulated in the hepatopancreas and muscles. A small amount of uric acid was detected in the hemolymph. This result suggests that Gln in muscles may be used as an intermediary nitrogen repository, while urea may be primarily synthesized in the hepatopancreas and then transferred to other tissues via the hemolymph. Uric acid could be synthesized by the anabolism of purine nucleotides, in additon to the inhibitory activities of gills. In addition, the levels of Gln, urea and uric acid exhibited dose-and time-dependent effects with ammonia content. Therefore, P. trituberculatus could possibly convert ammonia into Gln, urea, or uric acid to detoxify ammonia during high ambient ammonia-N stress.  相似文献   

15.
A feeding trial was carried out to investigate the dietary vitamin E requirement of the oriental river prawn Macrobrachium nipponense (weight of 0.3–0.4 g) and its effect role on antioxidant activity. Prawns were fed with seven levels of vitamin E (0, 25, 50, 75, 100, 200, and 400 mg/kg diet) for 60 days. The results show that dietary vitamin E supplementation could significantly increased the prawn weight (P < 0.05). The activity of superoxide dismutase (SOD) in the hepatopancreas was significantly higher in prawns fed with diets supplemented with ≤75 mg/kg vitamin E than in those fed with diets supplemented with 100–400 mg/kg vitamin E (P < 0.05). The activity of catalase (CAT) in the hepatopancreas decreased significantly as dietary vitamin E supplementation increased (P < 0.05), and no significant difference was detected in glutathione peroxidase (GSH-Px) activity between different dietary groups (P >0.05). The contents of vitamin E in the hepatopancreas and in the muscle increased with increasing dietary vitamin E. There was a linear correlation between the vitamin E level in diet and that in muscle, and between the vitamin E level in diet and that in the hepatopancreas. All the above results indicated that dietary vitamin E can be stored in the hepatopancreas and muscle and lower both the activities of SOD and CAT in the hepatopancreas, suggesting that it is a potential antioxidant in M. nipponense. Broken line analysis conducted on the weight gains of prawns in each diet group showed that the dietary vitamin E requirement for maximum growth is 94.10 mg/kg.  相似文献   

16.
【目的】探明无水保活流通过程中凡纳滨对虾(Litopenaeus vannamei)响应急冷(acute cold,AC)与空气暴露(waterless duration,WD)联合胁迫的生理代谢调节规律。【方法】研究模拟产业运输实际,分析联合胁迫(AC+WD)进程中凡纳滨对虾血液和肝胰腺典型生化指标,以及肝胰腺组织病理变化。【结果】AC胁迫后,凡纳滨对虾生理应激指标血清皮质醇含量由正常组(normal control,NC)的(326.90±4.61)pg/mL显著增加到AC组的(427.16±7.92)pg/mL(P<0.05),AC+WD组则随时间延长而逐渐降低。血清葡萄糖含量在联合胁迫6 h后达到最大值(26.31±1.05)mg/dL,乳酸在9 h达到峰值(7.90±0.11)mmol/L。AC及AC+WD组中血蓝蛋白、尿素氮和肌酐含量较NC组均发生不同程度的增加,而总蛋白含量先升后降,总胆固醇和甘油三酯含量呈胁迫时间依赖性下降。血清谷草转氨酶、谷丙转氨酶、酸性和碱性磷酸酶活力呈上升趋势,并在9 h达到峰值。以上生化指标在胁迫复苏组有所恢复,表明AC+WD双重胁迫引起凡纳滨对虾物质代谢紊乱,复苏后机体生理应激和代谢系统发生一系列代偿性调节,且胁迫进程中肝胰腺组织病理损伤特征进一步解释了凡纳滨对虾响应环境联合胁迫的结构基础。【结论】无水保活流通过程中双重胁迫时间依赖性改变凡纳滨对虾生理应激水平和物质代谢,在9 h时可明显造成肝胰腺组织结构损伤,进而影响机体存活。  相似文献   

17.
运用cDNA末端快速扩增(RACE)技术,克隆马氏珠母贝(Pinctadamαrtensii)热休克蛋白HSP60基因 cDNA全序列。序列全长2495坤,开放阅读框(ORF) 1734坤,编码577个氨基酸,预测的分子量约为61.79阳, 理论等电点为5.4905'非翻译区( 5'UTR)长150坤, 3'非翻译区(3'UTR)长611 bp。同源性比对分析结果,马 氏珠母贝HSP60基因与与太平洋长牡妨(Crωsos仰a gIgω)和光滑双蹄螺(Biomphalaria glabrata)的同源性较 高,达到75%。氨基酸序列分析显示,马氏珠母贝HSP60氨基酸序列具有典型的rnt-HSP60特征序列、C-末端典型的GGM重复基序和一个ATP结合结构域。荧光定量数据分析发现,该基因在闭壳肌、外套腹、血淋巴、肝膜腺、性腺、躁、等6个组织中具有表达,在肝膜腺中表达量最高,腮中次之,而在血液和闭壳肌中仅有少量表达;在脂多糖剌激后,该基因表达水平上调,12 h后达到最大值,之后又逐渐下调,均高于对照组,差异具统计学意 义(P〈0.05)。  相似文献   

18.
【目的】研究丁香酚在斜带髭鲷(Hapalogenys nitens)体内的代谢特点。【方法】通过麻醉效果实验确定适宜的麻醉浓度;于15、25℃水温条件下,将斜带髭鲷在适宜浓度的丁香酚溶液中药浴麻醉8 h,转入海水中复苏;采用GC-MS/MS法测定在麻醉和复苏过程鱼体血浆、肌肉、肝脏中丁香酚浓度,依欧洲药品管理局的动物可食用组织休药期指南计算休药期。【结果与结论】用于麻醉运输斜带髭鲷的丁香酚适宜质量浓度为7.5 mg/L。药浴温度为15℃时,血浆、肌肉、肝脏达峰时间(tmax)分别为2.0、3.0、5.0 h,达峰浓度(Cmax)分别为9.82、37.58、160.07 mg/kg;药浴温度为25℃时,血浆、肌肉、肝脏tmax分别为1.5、2.0、5.0 h,Cmax分别为12.75、46.80、185.20 mg/kg。在复苏过程中,鱼体丁香酚消除符合二室模型。15℃条件下,血浆、肌肉、肝脏中丁香酚平均驻留时间MRT(0-t)分别为6.464、4.001、6.670 h;25℃条件下,MRT(0-t)分别为6.076、3.756、5.791 h。丁香酚休药期为3 d。【结论】丁香酚在斜带髭鲷体内蓄积和消除速度快,经长时间丁香酚麻醉,丁香酚在鱼体内保持长时间低浓度存在。  相似文献   

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