ORIGINAL PAPERS

Effects of a high-fiber diet on energy metabolism in Niviventer lotipes

  • CHI Qingsheng ,
  • LUO Huining ,
  • YAO Xiaogang ,
  • LI Guangrong ,
  • YANG Changqian ,
  • ZHANG Qiang ,
  • LIU Yuhang ,
  • LIU Quansheng
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  • 1 College of Biology and Agriculture, Zunyi Normal University, Zunyi 563006, China;
    2 International Cooperation and Industry Development Center of Guizhou Forestry, Guiyang 550001, China;
    3 Guizhou Kuankuoshui National Nature Reserve, Suiyang 563300, China;
    4 Guangdong Institute of Applied Biological Resources, Guangzhou 510260, China

Received date: 2022-06-05

  Revised date: 2022-07-05

  Online published: 2023-01-10

Abstract

Small mammals usually show physiological adaptations to cope with seasonal changes in food quality. To examine the adaptive strategy in energy metabolism of Niviventer lotipes responding to varying dietary quality, we acclimated Niviventer lotipes to high-fiber standard rabbit pellets for 4 weeks with a group of animals fed with standard rat pellets as control. Body mass, parameters of energy intake, and expenditure were measured during the experiment. At the end of the experiment, animals were sacrificed to analyze the body composition. The results show that body mass of Niviventer lotipes fed with rabbit pellets decreased continuously and reached 62. 8% of that in control at the end of the experiment. Basal metabolic rate and nonshivering thermogenesis decreased significantly to 55. 1% and 63. 4% of the control respectively after the food treatment of 4 weeks. Food intake, digestive energy, and apparent digestibility also decreased to 63. 7%, 38. 8%, and 71. 8% of that in control, respectively. Body composition analysis showed that the mass and/or length of most vital organs and digestive tracts significantly decreased in animals fed with high-fiber rabbit pellets. Taken together, apparent digestibility decreased in Niviventer lotipes fed with a high-fiber diet, however, neither the mass/length of digestive tracts nor food intake increased to compensate for the decrease in digestive efficiency. Although the basal metabolic rate and nonshivering thermogenesis were down-regulated in animals fed with rabbit pellets, the energy balance cannot be maintained thus the body mass decreased significantly. This might be explained by the low selection pressure related to the utilization of a high-fiber food in the subtropical habitats of Niviventer lotipes.

Cite this article

CHI Qingsheng , LUO Huining , YAO Xiaogang , LI Guangrong , YANG Changqian , ZHANG Qiang , LIU Yuhang , LIU Quansheng . Effects of a high-fiber diet on energy metabolism in Niviventer lotipes[J]. ACTA THERIOLOGICA SINICA, 2023 , 43(1) : 11 -20 . DOI: 10.16829/j.slxb.150700

References

Bao Y X, Du W G, Lin Y, Jin W X. 1998. Energy metabolism and the morphology of digestive tract in Rattus niviventer confucianus and Rattus norvegicus. Acta Theriologica Sinica, 18 (3):202-207. (in Chinese)
Bao Y X, Du W G, Lin Z, Hu B Y, Chi B Y, Chen X D. 2001. Effect of temperature on energy requirement and food assimilation in Chinese white bellied rat (Niviventer confucianus). Acta Zoologica Sinica, 47 (5):597-600. (in Chinese)
Bao Y X. 1993. A summary of studies on Rattus niviventer. Journal of Zhejiang Normal University (Natural Science Edition), 16 (2):50-54. (in Chinese)
Bozinovic F, Novoa F F. 1997. Metabolic costs of rodents feeding on plant chemical defenses:a comparison between an herbivore and an omnivore. Comparative Biochemistry and Physiology, 117A:511-514.
Bozinovic F, Novoa F F, Sabat P. 1997. Feeding and digesting fiber and tannins by an herbivorous rodent Octodon degus (Rodentia:Caviomorpha). Comparative Biochemistry and Physiology, 118A:625-630.
Bozinovic F. 1992. Scaling of basal and maximum metabolic rate in rodents and the aerobic capacity model for the evolution of endo-thermy. Physiological Zoology, 65:921-932.
Bozinovic F. 1995. Nutritional energetics and digestive responses of an herbivorous rodent (Octodon degus) to different levels of dietary fiber. Journal of Mammalogy, 76:627-637.
Cannon B, Nedergaard J. 2004. Brown adipose tissue:function and physiological significance. Physiological Review, 84 (1):277-359.
Chi Q S, Wan X R, Geiser F, Wang D H. 2016. Fasting-induced daily torpor in desert hamsters (Phodopus roborovskii). Comparative Biochemistry and Physiology, 199A:71-77.
Choshniak I, Yahav S. 1987. Can desert rodents better utilize low quality roughage than their non-desert kindred? Journal of Arid Environments, 12 (3):241-246.
Cork S J. 1994. Digestive constraints on dietary scope in small and moderate-small mammals:how much do we really understand? In:Chivers D J, Langer P eds. The Digestive System in Mammals:Food, Form and Function. Cambridge University Press, Cam-bridge, 337-369.
Cruz-Neto A P, Bozinovic F. 2004. The relationship between diet qual-ity and basal metabolic rate in endotherms:insights from intraspe-cific analysis. Physiological and Biochemical Zoology, 77 (6):877-889.
Du W G, Bao Y X, Shi L Q, Yu H Y. 1999. Seasonal variations in weight and water content of vital organs in Rattus niviventer con-fucianus. Chinese Journal of Zoology, 34 (1):23-25. (in Chi-nese)
Du W G, Bao Y X. 2000. Seasonal variations in length and weight of the digestive tracts in Rattus niviventer confucianus and Rattus norvegicus. Acta Zoologica Sinica, 46 (3):271-277. (in Chinese)
Feng Z Y, Huang X Q, Yan S X. 1995. Study on the structure and suc-cession of farmland rodent community in pearl river delta. Supplement to the Journal of Sun Yatsen University, 3 (1):91-97.(in Chinese)
Foley W J, Cork S J. 1992. Use of fibrous diets by small herbivores:how far can the rules be ‘bent'? Trends in Ecology & Evolution, 7 (5):159-162.
Ge D Y, Lu L, Xia L, Du Y B, Wen Z X, Cheng J L, Abramov A V, Yang Q S. 2018. Molecular phylogeny, morphological diversity, and systematic revision of a species complex of common wild rat species in China (Rodentia, Murinae). Journal of Mammalogy, 99(6):1350-1374.
Grodzinski W, Wunder B A. 1975. Ecological energetics of small mammals. In:Golley F B, Petrusewicz K, Ryszkowski L eds. Small Mammals:Their Productivity and Population Dynamics. Cambridge:Cambridge University Press, 173-204.
Haim A, McDevitt R M, Speakman J R. 1995. Daily variations in the response of wood mice Apodemus sylvaticus to noradrenaline. Journal of Experimental Biology, 198 (2):561-565.
Hammond K A, Wunder B A. 1991. The role of diet quality and en-ergy need in the nutritional ecology of a small herbivore, Microtus ocbrogaster. Physiological Zoology, 64 (2):541-567.
Heldmaier G, Steinlechner S, Rafael J, Vsiansky P. 1981. Photoperi-odic control and effects of melatonin on nonshivering thermogen-esis and brown adipose tissue. Science, 212:917-919.
Heldmaier G, Steinlechner S, Rafael J. 1982. Nonshivering thermo-genesis and cold resistance during seasonal acclimatization in the Djungarian hamster. Journal of Comparative Physiology, 149:1-9.
Heldmaier G, Steinlechner S. 1981. Seasonal control of energy re-quirements for thermoregulation in the Djungarian hamster (Ph-odopus sungorus), living in natural photoperiod. Journal of Com-parative Physiology, 142:429-437.
Heldmaier G. 1971. Nonshivering thermogenesis and body size in mammals. Journal of Comparative Physiology, 73:222-248.
Hsi C H, Sun R Y. 1973. A study of the evaporative water losses of the brown and sulphur-bellied rats. Acta Zoologica Sinica, 19 (3):272-282. (in Chinese)
Jiang Z G, Liu S Y, Wu Y, Jiang X L, Zhou K Y. 2017. China's mam-mal diversity (2nd edition). Biodiversity Science, 25 (8):886-895. (in Chinese)
Juana C V, Cristina B, Alejandra A L M. 2006. Phenotypic plasticity in response to low quality diet in the South American omnivorous rodent Akodon azarae (Rodentia:Sigmodontinae). Comparative Biochemistry and Physiology, 145A:397-405.
Karasov W H, Diamond J M. 1988. Interplay between physiology and ecology in digestion. BioScience, 38:602-611.
Koteja P. 1996. Limits to the energy budget in a rodent, Peromyscus maniculatus:does gut capacity set the limits? Physiological Zool-ogy, 69:994-1020.
Li X S, Wang D H. 2005a. Regulation of body weight and thermogen-esis in seasonally acclimatized Brandt's voles (Microtus brandti). Hormones and Behavior, 48:321-328.
Li X S, Wang D H. 2005b. Seasonal adjustments in body mass and thermogenesis in Mongolian gerbils (Meriones unguiculatus):the roles of short photoperiod and cold. Journal of Comparative Physiology, 175B:593-600.
Liu Q S, Feng Z Y, Gong P B, Qin J, Gao Z X, Huang X L,Yao D D, Yan S X. 2010. Effects of high-fiber food on food intake and di-gestibility in the lesser rice-field rat (Rattus losea). Acta Therio-logica Sinica, 30 (3):291-296. (in Chinese)
Lu J Q, Zhang Z B. 2005. Food hoarding behavior of Chinese white-bellied rat (Niviventor confucianus). Acta Theriologica Si-nica, 25 (3):248-253. (in Chinese)
McNab B K. 1986. The influence of food habits on the energetics of eutherian mammals. Ecological Monographs, 56:1-19.
McNab B K. 2002. The Physiological Ecology of Vertebrates:A View from Energetics. Cornell University Press, Ithaca, N. Y.
Nagy T R, Negus N C. 1993. Energy acquisition and allocation in male collared lemmings (Dicrostonyx groenlandicus):effects of photoperiod, temperature, and diet quality. Physiological Zool-ogy, 66:537-560.
Peng P Y, Guo X G. 2014. The research status and progress of Nivi-ventor confucianus. Sichuan Journal of Zoology, 33 (5):792-800. (in Chinese)
Sibly R M. 1981. Strategies in digestion and defecation. In:Townsend C R, Calow P eds. Physiological Ecology. Sinauer, Sunderland, Mass, 109-139.
Silva S I, Jaksic F M, Bozinovic F. 2004. Interplay between metabolic rate and diet quality in the South American fox, Pseudalopex cul-paeus. Comparative Biochemistry and Physiology, 137A:33-38.
Sinclair A R E, Krebs C J, Smith J N M. 1982. Diet quality and food limitation in herbivores:the case of the snowshoe hare. Canadian Journal of Zoology, 60 (5):889-897.
Song Z G, Wang D H. 2002. Influencing factors on basal metabolic rate in mammals. Acta Theriologica Sinica, 22 (1):53-60. (in Chinese)
Sun R Y, Huang T H. 1973. Application of analysis of covariance in the study of oxygen consumption of two species of rats. Acta Zoologica Sinica, 19 (3):283-292. (in Chinese)
Van Sant M J, Hammond K A. 2008. Contribution of shivering and nonshivering thermogenesis to thermogenic capacity for the deer mouse (Peromyscus maniculatus). Physiological and Biochemi-cal Zoology, 81 (5):605-611.
Van Soest P J, Robertson J B, Lewis B A. 1991. Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in re-lation to animal nutrition. Journal of Dairy Science, 74 (10):3583-3597.
Veloso C, Bozinovic F. 1993. Dietary and digestive constraints on basal energy metabolism in a small herbivorous rodent. Ecology, 74:2003-2010.
Wei F W, Yang Q S, Wu Y, Jiang X L, Liu S Y, Li B G, Yang G, Li M, Zhou J, Li S, Hu Y B, Ge D Y, Li S, Yu W H, Chen B Y, Zhang Z J, Zhou C Q, Wu S B, Zhang L, Chen Z Z, Chen S D, Deng H Q, Jiang T L, Zhang L B, Shi H Y, Lu X L, Li Q, Liu Z, Cui Y Q, Li Y C. 2021. Catalogue of mammals in China (2021). Acta Therio-logica Sinica, 41 (5):487-501. (in Chinese)
Wunder B A. 1984. Strategies for, and environmental cueing mecha-nisms of, seasonal changes in thermoregulatory parameters of small mammals. In:Merritt J F ed. Winter Ecology of Small Mammals. Special Publication Carnegie Museum of Natural His-tory, Pittsburgh, 165-172.
Yu L F, Chen G P, Yu D L. 2018. The Biodiversity and Conservation in Kuankuoshui National Nature Reserve, Guizhou, China. Be-jing:China Forestry Publishing House, 8. (in Chinese)
Zhao Z J, Wang D H. 2007. Effects of diet quality on energy budgets and thermogenesis in Brandt's voles. Comparative Biochemistry and Physiology, 148A (1):168-177.
Zhao Z J, Wang D H. 2009. Plasticity in the physiological energetics of Mongolian gerbils is associated with diet quality. Physiologi-cal and Biochemical Zoology, 82 (5):504-5l5.
Zheng R Q, Bao Y X, Zhou H D, Chai J B, Huang X Q, Zheng X. 2003. Effect of photoperiod on digestibility and assimilation rate in the Chinese white-bellied rat (Niviventer confucianus). Acta Zoologica Sinica, 49 (4):525-528. (in Chinese)
冯志勇, 黄秀清, 颜世祥. 1995. 珠江三角洲稻作区农田鼠类群落结构及演替研究. 中山大学学报论丛 (生物学论文集), 3 (1):91-97.
刘全生, 冯志勇, 龚鹏博, 秦姣, 高志祥,黄小丽, 姚丹丹, 颜世祥. 2010. 高纤维食物对黄毛鼠摄食和消化的影响. 兽类学报, 30(3):291-296.
孙儒泳, 黄铁华. 1973. 褐家鼠和社鼠耗氧量研究中协方差分析的应用. 动物学报, 19 (3):283-292.
杜卫国, 鲍毅新, 施利强, 俞华英. 1999. 社鼠内脏器官重量和水分含量的季节变化. 动物学杂志, 34 (1):23-25.
杜卫国, 鲍毅新. 2000. 社鼠和褐家鼠消化道长度和重量的季节变化. 动物学报, 46 (3):271-277.
宋志刚, 王德华. 2002. 哺乳动物基础代谢率的主要影响因素. 兽类学报, 22 (1):53-60.
郑荣泉, 鲍毅新, 周慧娣, 柴君波, 黄学强, 郑祥. 2003. 光周期对社鼠能量摄入的影响. 动物学报, 49 (4):525-528.
奚家星, 孙儒泳. 1973. 褐家鼠和社鼠肺皮蒸发失水量的初步比较. 动物学报, 19 (3):272-282.
彭培英, 郭宪国. 2014. 社鼠的研究现状及进展. 四川动物, 33 (5):792-800.
蒋志刚, 刘少英, 吴毅, 蒋学龙, 周开亚. 2017. 中国哺乳动物多样性 (第2版). 生物多样性, 25 (8):886-895.
喻理飞, 陈光平, 余登利. 2018. 贵州宽阔水国家级自然保护区生物多样性保护研究. 北京:中国林业出版社, 8.
路纪琪, 张知彬. 2005. 围栏条件下社鼠的食物贮藏行为. 兽类学报, 25 (3):248-253.
鲍毅新, 杜卫国, 林治, 胡柏驿, 池帮荣, 陈孝端. 2001. 环境温度对社鼠能量需求和食物同化的影响. 动物学报, 47 (5):597-600.
鲍毅新, 杜卫国, 林奕, 金伟星. 1998. 社鼠和褐家鼠的能量代谢及消化道形态的比较. 兽类学报, 18 (3):202-207.
鲍毅新. 1993. 社鼠的研究概要. 浙江师大学报 (自然科学版), 2:50-54.
魏辅文, 杨奇森, 吴毅, 蒋学龙, 刘少英, 李保国, 杨光, 李明, 周江, 李松, 胡义波, 葛德燕, 李晟, 余文华, 陈炳耀, 张泽钧, 周材权, 吴诗宝, 张立, 陈中正, 陈顺德, 邓怀庆, 江廷磊, 张礼标, 石红艳, 卢学理, 李权, 刘铸, 崔雅倩, 李玉春. 2021. 中国兽类名录(2021版). 兽类学报, 41 (5):487-501.
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