Chair for Animal Nutrition and Dietetics, Department of Veterinary Sciences, Faculty of Veterinary Medicine, Ludwig-Maximilians-Universität München, Munich, Germany.
Core Facility Animal Models, Biomedical Center, Faculty of Medicine, Ludwig-Maximilians-Universität München, Munich, Germany.
Sci Rep. 2023 Oct 12;13(1):17299. doi: 10.1038/s41598-023-44532-6.
Alpha-amylase is the main enzyme for starch digestion in the mammalian gastrointestinal tract. There are species differences in the enzymatic activity of pancreatic amylase that are related to the digestive strategy and natural diet of a species. This aspect is well investigated in pet and farm animals, while in common laboratory animal rodents, information is scarce. In the context of the 3R concept, detailed knowledge of the digestive physiology should be the basis of adequate nutrition, experimental planning and data interpretation. The present study aimed to obtain reference data on amylase activity in pancreatic tissue and duodenal digesta in laboratory mice, rats and hamsters. In addition, digesta was stained with Lugol's iodine to visualize starch in the process of degradation throughout the gastrointestinal tract. Amylase activity in pancreatic tissue and duodenal digesta was significantly lower in hamsters than rats and mice. The Lugol staining showed intense starch degradation in the hamsters' forestomachs, presumably by microbial fermentation. A possible explanation is that the prae-duodenal microbial starch fermentation enhances digestibility and reduces the need for pancreatic amylase in hamsters. Rats and mice may rely more on pancreatic amylase for prae-caecal starch digestion, while the microbial fermentation is mainly located in the caecum. The results clearly show species differences in the digestive capacity for starch in mice, rats and hamsters that need to be considered in the feeding of these species in the laboratory setting as well as in the use of rodents as translational animal models.
α-淀粉酶是哺乳动物胃肠道中淀粉消化的主要酶。胰腺淀粉酶的酶活性存在物种差异,这与物种的消化策略和天然饮食有关。这方面在宠物和农场动物中得到了很好的研究,而在常见的实验室动物啮齿类动物中,信息却很少。在 3R 概念的背景下,详细了解消化生理学应该是适当营养、实验规划和数据解释的基础。本研究旨在获得有关实验室小鼠、大鼠和仓鼠胰腺组织和十二指肠内容物中淀粉酶活性的参考数据。此外,用卢戈氏碘对内容物进行染色,以可视化淀粉在整个胃肠道降解过程中的情况。与大鼠和小鼠相比,仓鼠胰腺组织和十二指肠内容物中的淀粉酶活性明显较低。卢戈氏碘染色显示仓鼠前胃中淀粉强烈降解,可能是通过微生物发酵。一种可能的解释是,十二指肠前微生物淀粉发酵提高了消化率,并减少了仓鼠对胰腺淀粉酶的需求。大鼠和小鼠可能更依赖胰腺淀粉酶来消化前盲肠淀粉,而微生物发酵主要位于盲肠中。研究结果清楚地表明,在淀粉消化能力方面,小鼠、大鼠和仓鼠存在物种差异,在实验室环境中饲养这些物种以及将啮齿类动物用作转化动物模型时,需要考虑这些差异。