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Experimental study on the effect of oral meloxicam administration in sows on pre-weaning mortality and growth and immunoglobulin G transfer to piglets

机译:口服甜美素蛋白施用在母猪中对仔猪预防死亡率和生长和免疫球蛋白G转移到仔猪的实验研究

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Parturation is an intrinsically risky and painful process for both the sow and the piglets that can cause welfare and economic problems. Non-steroidal antiinflammatory drugs (NSAIDs) have been demonstrated to partially alleviate inflammation and pain after farrowing in sows. NSAIDs effects on piglet mortality and performance show discrepancies and no previous studies have investigated the underlying mechanism. The effects of oral meloxicam treatment to sows on immunoglobulin G (IgG) transfer to piglets around farrowing were investigated. A total of 30 multiparous sows were randomly treated with either oral meloxicam or a mock administration as control group. Treatment was administered as soon as possible at the beginning of the farrowing. A total of 325 piglets were individually weighed at farrowing (day 0) and at weaning (day +21) and piglet mortality was registered during lactation. Four piglets per sow (two piglets suckling from anterior teats and two piglets suckling from posterior teats) were selected for blood sampling at day +1, day +2 and day +20 for IgG analyses. Oral meloxicam treatment to sows significantly increased weight at weaning (mean +/- SE: 6563 +/- 86.3 g from oral meloxicam group and 6145 +/- 103.2 g from control group; P = 0.0017) and ADG (mean +/- SE: 236 +/- 3.4 g/day from oral meloxicam group and 217 +/- 4.5 g/day from control group; P 0.001) during lactation, but failed to reduce piglet mortality during lactation (6.7% from oral meloxicam group and 6.8% from control group; P = 0.89). IgG levels in piglets from the sows treated with oral meloxicam were significantly higher than the control group at day +1 (mean; median [95% CI] for median = 31.9; 31.7 [29.6-33.6] vs. 27.9; 26.8 [25.9-28.3] mg/ml, P = 0.0013) and day +2 (27.6; 27.0 [24.8-29.6] vs. 24.5; 24.2 [22.1-25.3] mg/ml, P = 0.01). However, at day +20, IgG level in piglet serum was not significantly affected by the treatment (7.6; 7.6 [6.7-8.4] vs. 7.1; 6.9 [6.4-7.3] mg/ml, P = 0.59). The administration of meloxicam orally at the beginning of the farrowing in multiparous sows increased the concentration of IgG in serum of piglets and enhanced their pre-weaning growth. Future research is warranted to clearly identify the proximate mechanism behind IgG effect.
机译:批次是母猪和仔猪的内在风险和痛苦的过程,可能导致福利和经济问题。已经证明了非甾体类抗炎药(NSAIDs)以在母猪中训练后部分缓解炎症和疼痛。 NSAIDS对仔猪死亡率和性能的影响表现出差异,并且之前没有研究过的潜在机制。研究了口服甜美素治疗对免疫球蛋白G(IgG)转移到仔猪周围的仔猪转移的影响。用口服美洛昔康或模拟给药作为对照组随机处理总共30母猪。在击球开始时尽快施用治疗。共有325只仔猪在哺乳期(第0天)和断奶(日+21)时,在泌乳期间登记仔猪死亡率。为IgG分析的Day +1,Day + 2和Day +20,选择每母猪的四只仔猪(从前奶嘴和两只仔猪哺乳从后奶嘴哺乳)进行血液取样。口服Meloxicam治疗母猪的母猪在断奶中重量显着增加(平均+/- SE:6563 +/- 86.3g,来自甜美洛昔康组,对照组6145 +/- 103.2g; P = 0.0017)和ADG(平均+/- :从口服Meloxicam组的236 +/- 3.4克/日,对照组的217 +/- 4.5克/天; P <0.001)在哺乳期间,但未能在哺乳期间减少仔猪死亡率(来自口服墨西哥群组的6.7%)对照组6.8%; P = 0.89)。用口服甜美洛昔康治疗的母猪中仔猪中的IgG水平显着高于对照组(平均值;中位数[95%CI])= 31.9; 31.7 [29.6-33.6]与27.9; 26.8 [25.9- 28.3] Mg / ml,p = 0.0013)和Day + 2(27.6; 27.0 [24.8-29.6]与24.5; 24.2 [22.1-25.3] mg / ml,p = 0.01)。然而,在Day +20日,Piglet血清的IgG水平未受处理的显着影响(7.6; 7.6 [6.6 [6.7-8.4],7.1; 6.9 [6.4-7.3] mg / ml,p = 0.59)。 Meloxicam在多环母猪中施用于粉刺的开始时口服给药增加了仔猪血清IgG的浓度,并提高了它们预防预防生长。未来的研究是有必要清楚地确定IGG效应背后的近似机制。

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