方法:使用吞咽装置以非侵入方式研究猪肠道内容物的标准操作程序

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引用次数: 0

摘要

由于福利法的演变和对猪微生物群研究新方法的探索,开发精确的非侵入性采样方法是研究猪内脏微生物群落的关键。由于解剖学、对特定材料的要求以及需要约束动物等因素,给猪使用可吞咽装置始终是一项挑战。在本研究中,我们介绍了如何在不伤害动物的情况下给猪注射采样胶囊(CapSa)这一生物相容性非侵入性装置,以研究猪的微生物群。该方案通过两项不同的研究进行了验证。在研究 1 中,给 92 头瑞士大白猪(体重:6.45-71.3 千克)各注射了两粒胶囊,并在随后的 3 天内对其进行监测,以便取回胶囊。第 3 天,对所有猪实施安乐术,直接从其胃肠道中找到丢失的胶囊。在研究 2 中,16 头瑞士大白猪在断奶时被选中,并在五个不同的时间点(T1:52 ± 3;T2:70 ± 3;T3:83 ± 3;T4:110 ± 3;T5:126 ± 3 日龄)服用 CapSas。为了从粪便中提取胶囊,对给药后 3 天的猪进行了监测。到了 T5,猪被宰杀,从猪的胃肠道中取出粪便中未发现的 CapSas,称作丢失的 CapSas。该方案需要对动物进行适应性训练、调整饲养环境、使用促胃液分泌剂(普鲁卡必利)以促进胃排空,以及进行食道插管以克服与给药、胃阻塞和取回胶囊有关的挑战。在研究 1 中,46.74% 的给药 CapSas 在给药后 72 小时内出现在粪便中,47.67% 在最初 24 小时内被取回,28.26% 位于胃中。轻型猪(12 千克)的 CapSa 回收率最低。在研究 2 中,75.6% 的 CapSa 在给药后 72 小时内从粪便中回收,其中 51.23% 的 CapSa 在给药后 24 小时内回收。CapSa 的回收率因给药时间点的不同而不同,T1 和 T3 最低,T2 最高,T4 和 T5 处于中间值。在这两项研究中,pH值都受到运输时间的影响(P <0.01),当胶囊在36-40小时后排出时,pH值偏酸。在这两项研究中,除了研究 2 中的一头猪由于呼吸困难而被排除在外外,其他的死后观察结果均未显示与健康有关的问题。本研究描述了给猪注射 CapSa 或任何其他可吞咽装置的有效程序。此外,该程序还适用于在猪的一生中进行单次或重复给药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Method: Standard operating procedure for the administration of swallowable devices to study pig’s gut content in a non-invasive way

Due to the evolution of welfare laws and the search for novel methods to study pig microbiota, the development of precise and non-invasive sampling methods is key to studying the microbial communities that inhabit the guts of pigs. Administering swallowable devices to pigs is always a challenge due to factors such as anatomy, the requirement for specific materials, and the need to restrain the animals. In this study, we describe a step-by-step protocol on how to administer Capsule for Sampling (CapSa), a biocompatible non-invasive device to study pig’s microbiota without harming the animals. The validation of the protocol was done through two different studies. In Study 1, 92 Swiss Large White pigs (BW: 6.45–71.3 kg) were administered two capsules each and monitored for the following 3 days for capsule retrieval. On day 3, all pigs were euthanised to locate the missing capsules directly from their gastrointestinal tracts. In Study 2, 16 Swiss Large White pigs were selected at weaning and administered CapSas at five different timepoints (T1: 52 ± 3; T2: 70 ± 3; T3: 83 ± 3; T4: 110 ± 3; T5: 126 ± 3 days of age). To retrieve the capsules in the faeces, pigs were monitored 3 days postadministration. At T5, the pigs were slaughtered, and CapSas that were not found in the faeces, termed as missing CapSas, were retrieved from their gastrointestinal tracts. The protocol entails acclimation of the animals, housing modifications, administration of a prokinetic agent (prucalopride) to facilitate gastric emptying, and oesophageal intubations to overcome challenges related to administration, gastric blockage, and retrieval of the capsules. In Study 1, 46.74% of the administered CapSas were found in the faeces within 72 h postadministration, with 47.67% retrieved within the first 24 h, and 28.26% were located in the stomach. The CapSa retrieval was lowest in light pigs (<12 kg). In Study 2, 75.6% of CapSas were recovered in the faeces within 72 h postadministration, with 51.23% retrieved within the first 24 h. The CapSa retrieval rates varied depending on the administration time point being lowest at T1 and T3 and highest at T2 with intermediate values at T4 and T5. In both studies, the pH levels were affected by transit time (P < 0.01), resulting in a more acidic content when capsules were expelled after 36–40 h. To the contrary, the volume of the CapSa content was never affected by transit time (P < 0.05). In both studies, postmortem observations showed no health-related issues except one pig from Study 2 excluded due to respiratory distress. The present study describes a valid procedure for administering CapSa or any other swallowable devices in pigs. Moreover, this procedure is applicable to singular and repetitive administrations over the lifespan of pigs.

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