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1.
为研究不同给药方式下,恩诺沙星在中华草龟体内的药物代谢动力学规律。选取20只健康中华草龟,每组10只,随机分为2组,分别为肌注组和胃插管强制口服组,给药量均为10 mg/kg,应用液相色谱串联质谱法测定数据,Kinetic 4.4软件的非房室模型分析药时数据。胃插管强制口服给药主要药动学参数为C_(max)7.49μg/mL、T_(max) 12 h、T_(1/2)λz为99.85 h、AUC_(0-∞)为531.67 h~*μg/mL;肌注给药主要药动学参数为C_(max)5.85μg/mL、T_(max) 4 h、T_(1/2)λz为30.42 h、AUC_(0-∞)为193.6 h~*μg/mL。2种不同给药条件下,肌注恩诺沙星比胃插管强制口服更快达到最高血药浓度,表明肌注恩诺沙星在中华草龟体内吸收更快;胃插管强制口服给药的C_(max)和AUC均高于比肌注给药,表明胃插管强制口服恩诺沙星在中华草龟体内吸收更完全,分布更广泛效果更好。恩诺沙星在中华草龟体内消除缓慢,MRT长,胃插管强制口服给药MRT显著长于肌注给药,其血药浓度保留时间长,效果更持久。研究表明,需较快达到疗效时,建议肌注恩诺沙星;需持续给药且龟体代谢状态正常时,建议胃插管强制口服恩诺沙星;恩诺沙星在胃插管强制口服给药条件下,在中华草龟体内血药浓度高,保留时间长,生物利用度高,更适宜作为中华草龟个体疾病治疗的给药方式。  相似文献   

2.
为研究不同给药方式下,恩诺沙星在中华草龟体内的药物代谢动力学规律。选取20只健康中华草龟,每组10只,随机分为2组,分别为肌注组和胃插管强制口服组,给药量均为10 mg/kg,应用液相色谱串联质谱法测定数据,Kinetic 4.4软件的非房室模型分析药时数据。胃插管强制口服给药主要药动学参数为C_(max)7.49μg/mL、T_(max) 12 h、T_(1/2)λz为99.85 h、AUC_(0-∞)为531.67 h~*μg/mL;肌注给药主要药动学参数为C_(max)5.85μg/mL、T_(max) 4 h、T_(1/2)λz为30.42 h、AUC_(0-∞)为193.6 h~*μg/mL。2种不同给药条件下,肌注恩诺沙星比胃插管强制口服更快达到最高血药浓度,表明肌注恩诺沙星在中华草龟体内吸收更快;胃插管强制口服给药的C_(max)和AUC均高于比肌注给药,表明胃插管强制口服恩诺沙星在中华草龟体内吸收更完全,分布更广泛效果更好。恩诺沙星在中华草龟体内消除缓慢,MRT长,胃插管强制口服给药MRT显著长于肌注给药,其血药浓度保留时间长,效果更持久。研究表明,需较快达到疗效时,建议肌注恩诺沙星;需持续给药且龟体代谢状态正常时,建议胃插管强制口服恩诺沙星;恩诺沙星在胃插管强制口服给药条件下,在中华草龟体内血药浓度高,保留时间长,生物利用度高,更适宜作为中华草龟个体疾病治疗的给药方式。  相似文献   

3.
土霉素在奥尼罗非鱼体内的药动学研究   总被引:2,自引:0,他引:2  
在(21±1)℃的水温条件下,以50 mg/kg的单剂量,分别给奥尼罗非鱼(Oreochromis aureus×O.niloticus)水剂口灌和混饲口灌土霉素,用高效液相色谱法(HPLC)检测给药后各个时间点的血药浓度。结果显示:最低检测限为0.005μg/mL,线性范围为0.005~4μg/mL。水剂口灌组和混饲口灌组的药时数据均符合具时滞的二室开放动力学模型,水剂口灌组的动力学方程为:Ct=0.231e-0.028(t-0.010)+0.353e-0.011(t-0.010)-0.584e-0.468(t-0.010),混饲口灌组动力学方程:Ct=0.839e-0.057(t-0.459)+0.442e-0.013(t-0.459)-1.281e-0.282(t-0.459)。水剂口灌组及混饲口灌组主要药动学参数分别为:吸收半衰期(t1/2ka)为1.481 h,2.458 h;分布半衰期(t1/2α)为24.834 h,12.193 h;消除半衰期(t1/2β)为60.312 h,51.533 h;达峰时间(Tmax)为7.230 h,8.221 h;最大血药浓度(Cmax)为0.494μg/mL,0.796μg/mL;血药浓度-时间曲线下面积(AUC)=37.74μg.h/mL,43.075μg.h/mL。这些参数表明,水剂口灌比混饲口灌吸收快,分布和消除慢,在血液中达到峰浓度的时间更短,但峰浓度值比混饲口灌低。  相似文献   

4.
为研究不同给药方式下,恩诺沙星在中华草龟体内的药物代谢动力学规律。选取20只健康中华草龟,每组10只,随机分为2组,分别为肌注组和胃插管强制口服组,给药量均为10 mg/kg,应用液相色谱串联质谱法测定数据,Kinetic 4.4软件的非房室模型分析药时数据。胃插管强制口服给药主要药动学参数为C_(max)7.49μg/mL、T_(max) 12 h、T_(1/2)λz为99.85 h、AUC_(0-∞)为531.67 h~*μg/mL;肌注给药主要药动学参数为C_(max)5.85μg/mL、T_(max) 4 h、T_(1/2)λz为30.42 h、AUC_(0-∞)为193.6 h~*μg/mL。2种不同给药条件下,肌注恩诺沙星比胃插管强制口服更快达到最高血药浓度,表明肌注恩诺沙星在中华草龟体内吸收更快;胃插管强制口服给药的C_(max)和AUC均高于比肌注给药,表明胃插管强制口服恩诺沙星在中华草龟体内吸收更完全,分布更广泛效果更好。恩诺沙星在中华草龟体内消除缓慢,MRT长,胃插管强制口服给药MRT显著长于肌注给药,其血药浓度保留时间长,效果更持久。研究表明,需较快达到疗效时,建议肌注恩诺沙星;需持续给药且龟体代谢状态正常时,建议胃插管强制口服恩诺沙星;恩诺沙星在胃插管强制口服给药条件下,在中华草龟体内血药浓度高,保留时间长,生物利用度高,更适宜作为中华草龟个体疾病治疗的给药方式。  相似文献   

5.
通过肌内注射、口灌两种给药方式,研究氟苯尼考在罗非鱼体内的药物代谢动力学特征。把吉富罗非鱼(GIFT Oreochromis niloticus)随机分成2组,控制水温在30℃,以15 mg/kg分别单剂量肌内注射、口灌给药。经高效液相色谱法(HPLC)测定血浆中氟苯尼考浓度,用Win Nonlin药动学软件分析药动学参数。结果表明:肌内注射氟苯尼考后,药物吸收较慢,消除较快,达峰时间(T_(max))=4 h,峰浓度(C_(max))=4.64μg/mL,消除半衰期(T_(1/2λ)z L)=10.45 h,药-时曲线下面积(AUC)=91.06μg·h/mL。口灌氟苯尼考后,药物吸收较快,消除较慢,T_(max)=1 h,C_(max)=5.92μg/mL,T_(1/2λ)z L=13.13 h,AUC=61.96μg·h/mL。肌内注射、口灌氟苯尼考后,二者的药动学参数差异显著,这一差异表明肌内注射给药吸收相对较慢,但更为完全(肌内注射氟苯尼考的AUC明显较大),消除相对较快。  相似文献   

6.
在(20±1)℃的水温条件下,以77 mg/kg的单剂量,给异育银鲫(Carassius auratus gibelio)口灌诃子(Fructus chebulae)水剂,以诃子中的主要成分没食子酸为检测目标,用高效液相色谱法(HPLC)检测给药后各个时间点的血药浓度。结果显示:最低检测限为0.01μg/mL,线性范围为0.01~84.00μg/mL。诃子在异育银鲫体内的药动学过程符合一级吸收二室开放房室模型(1/C/C),其药物动力学方程为C=39.237e-0.320t+4.814e-0.006t,主要药动学参数为:吸收速率常数(Ka)为0.56 h-1,吸收半衰期(t1/2ka)为1.238 h,分布半衰期(t1/2α)为2.164 h,消除半衰期为(t1/2β)为119.369 h,达峰时间(Tmax)为4 h,最大血药浓度(Cmax)为11.024μg/mL,血药浓度-时间曲线下面积(AUC(0-∞))=674.89μg.h/mL,延滞时间(TL)为0.286 h,药物平均滞留时间(MRT(0-∞))=113.626 h,总体消除率(CLs)为0.112 L/(kg.h),表观分布容积(Vd)为13.713 L/kg。这些参数表明,异育银鲫口灌诃子后,能比较迅速被吸收,并且在血浆中维持较长的时间,具有较好的应用价值基础。  相似文献   

7.
土霉素在黑鲷体内的药物代谢动力学研究   总被引:10,自引:0,他引:10  
首次报道了黑鲷口服土霉素的药物代谢动力学特征,用高效液相色谱法测定组织中的药物含量,药物在肌肉,血液,肝脏中的平均回归率分别为85.61%,85.38%,82.005,该方法的检测限可达0.01μg/g,黑鲷1次口服剂量为75mg/kg的土壤素后,其血液药物浓度-时间数据符合一室开放动力学模型,吸收速率常数(ka)为0.296/h,达峰时间(Tamx)为10.635h,峰浓度(Cmax)为1.398μg/ml, 分布半衰期(T1/2a)为2.339h ,消除半衰期(T1/20β)为46.663h,药时曲线下面积(AUC)为110.25mg/L.h,黑绸口服药物0.5h后在血液,肥肉,肝脏,肾脏4种组织中就可以检测到药物的存在,药物在16h的采样点浓度达最高,分别为1.68μg/ml,1.68,2.52,6.77μg/g。  相似文献   

8.
在(10±1)℃水温条件下,研究了土霉素(OTC)经肌肉注射和口灌给药后在鲫体内的药物动力学。将试验鲫随机分为两组:一组采用肌肉注射,另一组采用口灌,两组给药剂量都为50 mg/kg。结果表明:吸收半衰期t1/2(kα)、分布半衰期t1/2(kα)和消除半衰期t1/2(kα)在口灌给药时分别为3.83 h、3.98 h和129.04 h,而在肌肉注射给药时分别为1.58 h、1.71 h、和98.61 h,说明肌肉注射时OTC在鲫体内的吸收、分布和消除比口灌时快;口灌和肌肉注射时,达峰时间分别为15.47 h和7.78 h,肌肉注射的最大药物浓度(12.04μg/mL)比口灌时高(7.20μg/mL)。  相似文献   

9.
研究了不同水温(16℃、25℃)、不同给药剂量(10 mg/kg、20 mg/kg)和不同给药方式(肌注、口灌)等条件下,恩诺沙星及其代谢产物环丙沙星在中华绒螯蟹体内的药代动力学,比较了不同条件下药物在蟹血淋巴中的吸收、分布和代谢的差异。结果表明,恩诺沙星在蟹血淋巴中的药-时数据符合开放式二室模型。16℃时以10 mg/kg剂量肌注给药后,恩诺沙星在蟹血淋巴的主要药代动力学参数为:AUC96.818 mg/(L.h),Cmax6.54μg/mL,t1/2α0.851 h,t1/2β95.415 h;25℃时以10 mg/kg剂量肌注给药后,恩诺沙星的主要药代动力学参数为:AUC168.457 mg/(L.h),Cmax7.12μg/mL,t1/2α0.58h,t1/2β88.833 h;25℃时以20 mg/kg剂量肌注给药后,恩诺沙星的主要药代动力学参数为:AUC155.612 mg/(L.h),Cmax11.045μg/mL,t1/2α5.239h,t1/2β88.378 h;25℃时以10 mg/kg剂量口灌给药后,恩诺沙星的主要药代动力学参数为:AUC86.525 mg/(L.h),Cmax3.469μg/mL,t1/2α8.071h,t1/2β61.842 h。不同条件下,恩诺沙星在蟹血淋巴中的主要药代动力学参数差异较大。恩诺沙星的活性代谢产物环丙沙星在各种给药条件下的蟹血淋巴中均能检出,但含量均处于较低值,且药-时数据不能用房室模型拟合,表明恩诺沙星在蟹体内只有极少部分代谢为环丙沙星。  相似文献   

10.
盐酸诺氟沙星在奥尼罗非鱼体内的药动学研究   总被引:4,自引:3,他引:1  
按照鱼的体重,以10 mg/kg的单剂量,分别给奥尼罗非鱼(Oreochromis aureus×O.niloticus)水剂口灌和混饲口灌盐酸诺氟沙星,用高效液相色谱法(HPLC)检测给药后各个时间点的血药浓度。结果显示:水剂口灌组和混饲口灌组的药时数据符合开放性二室模型,水剂口灌组药物的吸收、消除都明显快于混饲组,水剂口灌组主要药动学参数为:t1/2ka=0.269 h,t1/2α=0.588 h,t1/2β=16.42 h,Tmax=0.745 h,Cmax=0.123μg/mL,AUC=1.83 h;混饲口灌组主要药代动力学参数:t1/2ka=0.428 h,t1/2α=1.85 h,t1/2β=21.77 h,Tmax=1.63 h,Cmax=0.099μg/mL,AUC=2.42 h。  相似文献   

11.
Successful immobilisation of Przewalski's horses and zebras was obtained by using a combination of STH 2130 (Boehringer) and Tiletamin/Zolazepam.  相似文献   

12.
The immobilisation of 25 wild boars with a combination of tiletamine/zolazepam/romifidine is described. The applied dose was 3-6 mg/kg BW Tilest 500 and 100 micrograms/kg BW Sedavet. The mean recumbency time was 5-10 min. There were no critical moments during anesthesia, even with pregnant sows. Anesthesia was supervised with a pulse oximeter and a respiration frequency monitor. The oxygen saturation was between 92% and 96%, pulse and respiration rate remained normal.  相似文献   

13.
王济秀  张锋  王卫民  刘红 《水产学报》2020,44(4):528-538
为探索鱼类转铁蛋白基因tf和转铁蛋白受体基因tfr1a的转录调控机制,本实验以团头鲂为研究对象,在其全基因组数据库中获取tf和tfr1a基因序列,对2个基因候选启动子区转录因子结合位点及CpG岛进行预测,通过PCR方法克隆得到tf和tfr1a基因近端启动子区不同长度片段,连接至pGL3-Basic/pEGFP-1载体,瞬时转染入Hela细胞,并采用双荧光素酶报告基因检测系统进行检测。结果发现,团头鲂tf基因启动子区无CpG岛位点,而tfr1a基因启动子区有2个CpG岛位点。成功构建9个tf和10个tfr1a不同长度启动子片段的重组质粒,经双荧光素酶报告基因系统检测发现,tf启动子核心区域为-268^+56 bp,且-1 308^-1 102 bp片段可能存在正调控该基因表达的转录因子结合位点;tfr1a启动子核心区域为-224^+48 bp,且+48^+92 bp可能存在抑制该基因转录的负调控元件,而-1 229^-1 219 bp区域可能存在促进tfr1a基因表达的正调控转录因子结合位点。  相似文献   

14.
The effect of Microbacterium sp. strain 8L and Exiguobacterium mexicanum strain 8N was evaluated in the diet of Artemia under xenic conditions. Viable cultures of bacteria were provided to xenic cultures of Artemia in combination with Sacharomyces cerevisiae, cornflour or Spirulina, and the effect on the survival and growth was recorded. The use of these bacterial strains improves significantly the survival of Artemia independently of the used food (P < 0.05), and variable results were observed in the growth.  相似文献   

15.
为探讨养殖水体底栖鱼类肠道排泄物对铜绿微囊藻休眠体复苏的影响,将青鱼和鲇肠道排泄物与铜绿微囊藻休眠体用野外养殖水域沉积物(底泥)混匀包埋,在10、15和20°C梯度温度下进行休眠体复苏实验。结果显示,铜绿微囊藻休眠体主要复苏期为第3~15天,在10和15°C条件下,青鱼排泄物组(MP)、鲇排泄物组(SA)和青鱼-鲇排泄物混合组(MP-SA)铜绿微囊藻休眠体复苏率均显著高于对照组(CK),且MP组也显著高于SA组和MP-SA组;在20°C条件下,MP组铜绿微囊藻休眠体复苏率显著高于SA组、MP-SA混合组和CK组,但SA组和MP-SA组与CK组复苏率并无显著性差异。实验过程中MP组沉积物中优势菌群以假单胞菌为主,SA组和MP-SA组优势菌群分别以芽孢杆菌和厚壁菌为主,第0~12天为菌群增殖期,且此期间沉积物-水体界面(SWI)实验MP组、SA组和MP-SA组溶解氧含量(DO)和氮磷比(N/P)均显著低于对照组。研究表明,青鱼和鲇肠道排泄物能促进铜绿微囊藻休眠体复苏,且这种促复苏效果在低温区间(10~15°C)更显著,可能是排泄物中菌群在生长增殖期降低了沉积物-水体界面N/P和DO的结果。研究结果对养殖水体底泥清淤和春季铜绿微囊藻水华防控具有一定的理论意义。  相似文献   

16.
溶藻弧菌相关分离株的分子及VITEK鉴定   总被引:1,自引:0,他引:1  
哈维群弧菌是弧菌属的核心菌群,包括溶藻弧菌在内的6个种在表型和遗传型上均十分相似,要准确鉴定各种有一定难度。看家基因的研究及生化鉴定系统的出现为弧菌鉴定提供了多种方法,本文比较了16S rRNA基因、toxR基因和pyrH基因以及VITEK 2 COMPACT GN鉴定卡对溶藻弧菌相关分离株的分辨力。哈维群弧菌基因组内16S rRNA基因是多拷贝的,且拷贝间序列差异大于种间差异,不适用于种的鉴定。单拷贝基因toxR和pyrH序列种内差异均小于种间差异。基于toxR基因相似性比较可清楚地将18个疑似溶藻弧菌分离株和5个参比株归并到4个种;toxR基因系统发育学分析也显示,哈维群弧菌各种独立地聚类分支,且溶藻弧菌种内存在两个明显的聚类分支,说明两个分支的溶藻弧菌具有独立的进化方向。pyrH基因的相似性比较和发育学分析也得到类似的结果,但pyrH基因具有较强的保守性,因而分辨力稍低于toxR基因。VITEK 2 COMPACT GN鉴定卡在鉴定溶藻弧菌时也有一定的错误率,且鉴定谱较窄。因此,建议在实际应用中采用toxR基因比对作为溶藻弧菌快速鉴定的主要手段,可再选用pyrH基因对鉴定结果进行验证。  相似文献   

17.
养殖大菱鲆中牙鲆肠弧菌的分离鉴定及组织病理学   总被引:5,自引:0,他引:5  
2007年1月,山东省胶南某养殖场人工养殖的大菱鲆(Scophthalmus maximus)发生严重病害并大批死亡。病鱼的主要症状是体表溃疡,腹腔积液,肠道肿胀,肝脏萎缩,胆囊暗绿色等。从病鱼胆囊中分离纯化得到优势菌株,命名为da3。人工感染试验证实,该菌株对大菱鲆有较强的致病性。对体重为25 g的大菱鲆的半数致死量为每尾鱼2×106 cfu。通过细菌16S rDNA序列测定及形态学和生理生化特征研究确定,该病原菌为牙鲆肠弧菌(Vibrio ichthyoenteri)。组织病理学观察表明,病鱼的肝脏、肾脏、脾脏、肠道和脑的微观结构发生了明显的病理变化,由此引起的器官功能衰竭可能是病鱼死亡的主要原因。本文结果对大菱鲆细菌性病害的控制具有参考价值。  相似文献   

18.
Growth experiments carried out with two juvenile crayfish species, Astacus leptodactylus Eschscholtz and Pacifastacus leniusculus (Dana), at different temperatures and densities highlighted the problem of cannibalism under conditions aimed at intensifying crayfish production. Cannibalism proved to be much lower in A. leptodactylus than P. leniusculus, suggesting that the former might be the better candidate for astaciculture. In the first of two population survival trials, A. leptodactylus showed a higher survival rate than P. leniusculus, with 26% of P. leniusculus surviving in the first replicate, compared to 42.3% of P. leniusculus, and 40.76% surviving in the second replicate, compared to 47.6% of P. leniusculus. The same trend was observed in the second experiment, with P. leniusculus showing survival rates of 48.5 and 55.3% (first and second replicates, respectively) in comparison to 65.2 and 68.2%, respectively, for A. leptodactylus. It is therefore highly likely that if P. leniusculus were to become established in Turkey, it would outcompete the native A. leptodactylus even if it were not to be devastated by the crayfish plague that has decimated the native species. The experiments also highlighted the problem of differential growth, with some juveniles hardly growing at all while others reached a relatively large size. The range in carapace length (CL) was 9–18 mm for A. leptodactylus and 8.5–18.5 mm CL for P. leniusculus at the end of the first experiment. While both species grew quickly, P. leniusculus hatched earlier, giving it an advantage over A. leptodactylus; consequently, by the end of the summer, the juveniles of the former were larger than those of A. leptodactylus. Specific growth rate values showed that the juveniles of the two species had similar growth rates. The results also revealed that growth was not significantly affected by density in both species at 15°C, but at 25°C, growth was significantly better at a density of 234 juveniles m−2 than at 468 juveniles m−2, and better at 468 juveniles m−2 than at 937 juveniles m−2 (P < 0.01 and P < 0.001, respectively). We conclude that P. leniusculus is a good candidate for aquaculture as it has a rapid growth rate and early hatching and maturity; however, its aggressive behavior may make it a less attractive proposition than A. leptodactylus, which is also fast growing but less aggressive. This study is a part of PhD study of M.M. Harlıoğlu, who is supported by Fırat University Elazığ, Turkey.  相似文献   

19.
半滑舌鳎TRAF6 基因和TAK1 基因的克隆及表达分析   总被引:1,自引:1,他引:0  
本研究通过同源克隆和RACE技术获得了半滑舌鳎(Cynoglossus semilaevis)肿瘤坏死因子受体相关因子6(tumor necrosis factor receptor-associated factor 6,TRAF6)和转化生长因子β激活激酶1(transforming growth factor-β-activated kinase 1,TAK1)的c DNA全长,并分析了其在不同组织和早期胚胎发育时期的表达情况。结果表明,TRAF6 c DNA全长1956 bp,开放阅读框(ORF)为1731 bp,编码576个氨基酸。二级结构预测显示TRAF6具有保守的蛋白结构域:N端的RING结构,两个锌指结构以及C端的环–环(coiled-coil)α螺旋结构和高度保守的MATH同源结构。TAK1 c DNA全长2519 bp,ORF为1731 bp,编码576个氨基酸。TAK1的蛋白结构域包括丝氨酸/苏氨酸蛋白激酶激活结构域和C端的环–环(coiled-coil)α螺旋结构域。系统进化树分析表明,半滑舌鳎TRAF6和TAK1分别与牙鲆(Paralichthys olivaceus)TRAF6和TAK1聚为一支,亲缘关系最近。荧光定量PCR结果显示,TRAF6和TAK1在所检测的8种组织中都有表达,TRAF6在鳃中的表达最高,肠中也有较高的表达;TAK1在心脏中的表达量最高,其次是肾。TRAF6和TAK1在鳃、肾等免疫器官中的高表达,与其在Toll样受体信号通路中的重要作用是一致的。对TRAF6和TAK1在早期胚胎发育时期的表达情况进行检测,结果显示,在未受精卵中可检测到TRAF6和TAK1,提示了这两种免疫分子的母源性m RNA遗传的可能性。免疫分子母源性m RNA可能参与发育过程,也可能参与构建免疫体系,以保护胚胎或仔鱼免受病原体的侵袭。  相似文献   

20.
One of the major problems in the shrimp culture industry is the difficulty in producing high-quality shrimp larvae. In larviculture, quality feeds containing a high content of highly unsaturated fatty acids (HUFA) and ingredients that stimulate stress and disease resistance are essential to produce healthy shrimp larvae. In the present study, Penaeus monodon postlarvae (PL15) were fed for 25 days on an unenriched Artemia diet (control; A) or on a diet of Artemia enriched with either HUFA-rich liver oil of the trash fish Odonus niger (B), probionts [Lactobacillus acidophilus (C1) or yeast-Saccharomyces cerevisiae (C2)] or biomedicinal herbal products (D) that have anti-stress, growth-promoting and anti-microbial characteristics. P. monodon postlarvae fed unenriched Artemia exhibited the lowest weight gain (227.9 ± 8.30 mg) and specific growth rate (9.95 ± 0.05%), while those fed the HUFA-enriched Artemia (B) exhibited the highest weight gain and specific growth rate (362.34 ± 12.56 mg and 11.77 ± 0.08%, respectively). At the end of the 25-day rearing experiment, the shrimp postlarvae (PL40) were subjected to a salinity stress study. At both low and high (0 and 50‰) salinities, the group fed the control diet (A) experienced the highest cumulative mortality indices (CMI) 935.7 ± 2.1 and 1270.7 ± 3.1, respectively. Those fed diet D showed the lowest stress-induced mortality, and CMI were reduced by 31.1 and 32.3% under conditions of low and high salinity stress, respectively. A 10-day disease challenge test was conducted with the P. monodon postlarvae (PL40–PL50) by inoculating the shrimp with the pathogen Vibrio harveyi at the rate of 105–107 CFU/ml in all rearing tanks. P. monodon postlarvae fed probiont-encapsulated Artemia diets (C1 and C2) exhibited the highest survival (94.3 and 82.3%, respectively) and lowest pathogen load (V. harveyi) in hepatopancreas (5.2 × 102 ± 9.0 × 10 and 4.6 × 102 ± 9.0 × 10 CFU g−1, respectively) and muscle (2.0 × 102 ± 6 × 10 and 1.7 × 102 ± 8.6 × 10 CFU g−1, respectively) tissues. The shrimp that were fed the unenriched Artemia (Control; A) showed the lowest survival (26.33%) and highest bacterial load in the hepatopancreas (1.0 × 105 ± 5 × 103 CFU g−1) and muscle (3.6 × 104 ± 6 × 102 CFU g−1). The shrimp fed the herbal product (D)-enriched Artemia also exhibited enhanced survival and reduced V. harveyi load in the tissues tested compared to the control diet (A) group. The results are discussed in terms of developing a quality larval feed to produce healthy shrimp larvae.  相似文献   

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