基于食物安全视角的我国畜产食品进口依赖性风险评价     

吴渊  高颂  高雅灵  林慧龙 《草业学报》2018,27(10):171-182

新时期下,保障我国畜产食品供给安全是保障我国食物安全的重要内容之一,而“适度进口”是保障我国畜产食品供给安全的重要途径之一。如何才算“适度进口”,需对畜产食品进口的相关风险进行分析方可评判。运用进口依赖性评价模型对我国猪肉、鸡肉、羊肉、牛肉、鲜牛奶的进口依赖性风险进行分析发现,上述5种畜产食品均存在进口依赖性风险。其中,猪肉的风险来自美国、德国、丹麦、西班牙和加拿大;鸡肉的风险来自美国、巴西、阿根廷和波兰;羊肉的风险来自澳大利亚、新西兰和乌拉圭;牛肉的风险来自乌拉圭、澳大利亚、新西兰、阿根廷和加拿大;鲜牛奶的风险来自德国、法国、新西兰和澳大利亚。为降低我国畜产食品进口依赖性风险,短期内应采取畜产食品进口市场多元化策略以及用进口饲草料替代进口畜产食品的进口方式;长期应在保障“口粮安全”的前提下,调整农业结构,大力发展草地农业,减少对国际市场的依赖性。  相似文献   

Virus‐neutralising antibody responses in horses following vaccination with Equivac® HeV: a field study          下载免费PDF全文

RHH Tan  A Hodge  R Klein  N Edwards  JA Huang  D Middleton  SP Watts 《Australian veterinary journal》2018,96(5):161-166

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Effect of pre‐milking teat disinfection on clinical mastitis incidence in a dairy herd in Northern Queensland,Australia          下载免费PDF全文

SM Rowe  WP Tranter  RA Laven 《Australian veterinary journal》2018,96(3):69-75

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Impact of Grasshopper Control on Forage Quality and Availability in Western Nebraska     

Jeffrey D. Bradshaw  Karla H. Jenkins  Sean D. Whipple 《Herpetological Monographs》2018,40(3):71-76

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Discovering new areas of veterinary science through qualitative research interviews: introductory concepts for veterinarians          下载免费PDF全文

CF May 《Australian veterinary journal》2018,96(8):278-284

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Soft tissue sarcoma in a short‐beaked echidna (Tachyglossus aculeatus)          下载免费PDF全文

RL Robey  C Sangster  M Gabor  SA Lindsay 《Australian veterinary journal》2018,96(9):360-365

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Effect of benazepril and pimobendan on serum angiotensin‐converting enzyme activity in dogs          下载免费PDF全文

J. N. King  C. Christinaz  G. Strehlau  J. Hornfeld 《Journal of veterinary pharmacology and therapeutics》2018,41(3):485-489

To support their combined use, the objective of the study was to evaluate the effects of benazepril and pimobendan on serum angiotensin‐converting enzyme (ACE) activity in dogs. A total of 48 healthy beagle dogs were randomized into four groups (n = 12 per group) in a parallel‐group design study: A (control, placebo twice daily (BID)); B (0.5–1.0 mg/kg benazepril once daily (SID) in the morning, placebo in the evening); C (0.25–0.5 mg/kg benazepril BID); D (0.25–0.5 mg/kg benazepril and 0.125–0.25 mg/kg pimobendan, both BID). The test items were administered orally for 15 days. Serum ACE activity was measured on days 1 and 15. Groups B, C and D had significantly lower average serum ACE activity compared to baseline and to the control group, on both days 1 and 15. There were no significant differences in average ACE activity between groups B, C and D. Noninferiority of group C to B was demonstrated. In conclusion, 0.25–0.5 mg/kg benazepril administered BID produced noninferior inhibition of serum ACE activity compared to 0.5–1.0 mg/kg benazepril dosed SID. Pimobendan had no significant effect on benazepril's action on serum ACE activity. The results support the use of benazepril BID in dogs and in combination with pimobendan.  相似文献   

Integration of pharmacokinetic–pharmacodynamic for dose optimization of doxycycline against Haemophilus parasuis in pigs          下载免费PDF全文

Y. Wang  A. Sajid  S. Ahmed  X. Li 《Journal of veterinary pharmacology and therapeutics》2018,41(5):706-718

The aims of this study were to establish optimal doses of doxycycline (dox) against Haemophilus parasuis on the basis of pharmacokinetic–pharmacodynamic (PK‐PD) integration modeling. The infected model was established by intranasal inoculation of organism in pigs and confirmed by clinical signs, blood biochemistry, and microscopic examinations. The recommended dose (20 mg/kg b.w.) was administered in pigs through intramuscular routes for PK studies. The area under the concentration 0‐ to 24‐hr curve (AUC_0–24), elimination half‐life (T_½ke), and mean residence time (MRT) of dox in healthy and H. parasuis‐infected pigs were 55.51 ± 5.72 versus 57.10 ± 4.89 μg·hr/ml, 8.28 ± 0.91 versus 9.80 ± 2.38 hr, and 8.43 ± 0.27 versus 8.79 ± 0.18 hr, respectively. The minimal inhibitory concentration (MIC) of dox against 40 H. parasuis isolates was conducted through broth microdilution method, the corresponding MIC₅₀ and MIC₉₀ were 0.25 and 1 μg/ml, respectively. The Ex vivo growth inhibition data suggested that dox exhibited a concentration‐dependent killing mechanism. Based on the observed AUC_24 hr/MIC values by modeling PK‐PD data in H. parasuis‐infected pigs, the doses predicted to obtain bacteriostatic, bactericidal, and elimination effects for H. parasuis over 24 hr were 5.25, 8.55, and 10.37 mg/kg for the 50% target attainment rate (TAR), and 7.26, 13.82, and 18.17 mg/kg for 90% TAR, respectively. This study provided a more optimized alternative for clinical use and demonstrated that the dosage 20 mg/kg of dox by intramuscular administration could have an effective bactericidal activity against H. parasuis.  相似文献   

Pharmacokinetics of multiple doses of transdermal flunixin meglumine in adult Holstein dairy cows          下载免费PDF全文

M. D. Kleinhenz  P. J. Gorden  J. S. Smith  J. A. Schleining  K. E. Kleinhenz  L. L. Wulf  P. K. Sidhu  D. Rea  J. F. Coetzee 《Journal of veterinary pharmacology and therapeutics》2018,41(3):490-493

A transdermal formulation of the nonsteroidal anti‐inflammatory drug, flunixin meglumine, has been approved in the United States and Canada for single‐dose administration. Transdermal flunixin meglumine was administered to 10 adult Holstein cows in their second or third lactation at the label dose of 3.33 mg/kg every 24 hr for three total treatments. Plasma flunixin concentrations were determined using high‐pressure liquid chromatography with mass spectroscopy (HPLC ‐MS ). Pharmacokinetic analysis was completed on each individual animal with noncompartmental methods using computer software. The time to maximum drug concentration (T max) was 2.81 hr, and the maximum drug concentration was 1.08 μg/ml. The mean terminal half‐life (T½) was determined to be 5.20 hr. Clearance per fraction absorbed (Cl/F) was calculated to be 0.294 L/hr kg^?1, and volume of distribution of fraction (V z/F ) absorbed was 2.20 L/kg. The mean accumulation factor was 1.10 after three doses. This indicates changes in dosing may not be required when giving multiple doses of flunixin transdermal. Further work is required to investigate the clinical efficacy of transdermal flunixin after multiple daily doses.  相似文献   

Comparison between the urine dipstick and the pH‐meter to assess urine pH in sheep and dogs          下载免费PDF全文

Labrini V. Athanasiou  Panagiotis D. Katsoulos  Eleni G. Katsogiannou  Zoe S. Polizopoulou  Myrto Diamantaki  Constantinos Kamatsos  Georgios Christodoulopoulos 《Veterinary clinical pathology / American Society for Veterinary Clinical Pathology》2018,47(2):284-288

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