The effects of a hydrolyzed protein diet on the plasma, fecal and urine metabolome in cats with chronic enteropathy

被引:3
作者
Kathrani, Aarti [1 ]
Yen, Sandi [2 ]
Hall, Edward J. [3 ]
Swann, Jonathan R. [4 ,5 ]
机构
[1] Royal Vet Coll, Hawkshead Lane, Hatfield AL9 7TA, Herts, England
[2] Univ Oxford, Kennedy Inst Rheumatol, Oxford Ctr Microbiome Studies, Oxford OX3 7FY, England
[3] Univ Bristol, Bristol Vet Sch, Bristol BS40 5DU, Avo, England
[4] Univ Southampton, Sch Human Dev & Hlth, Fac Med, Southampton SO16 6YD, England
[5] Imperial Coll London, Dept Metab Digest & Reprod, London SW7 2AZ, England
关键词
INFLAMMATORY-BOWEL-DISEASE; COLITIS; DOGS; PROFILES; DIAGNOSTICS; SERUM;
D O I
10.1038/s41598-023-47334-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hydrolyzed protein diets are extensively used to treat chronic enteropathy (CE) in cats. However, the biochemical effects of such a diet on feline CE have not been characterized. In this study an untargeted H-1 nuclear magnetic resonance spectroscopy-based metabolomic approach was used to compare the urinary, plasma, and fecal metabolic phenotypes of cats with CE to control cats with no gastrointestinal signs recruited at the Royal Veterinary College (RVC). In addition, the biomolecular consequences of a hydrolyzed protein diet in cats with CE was also separately determined in cats recruited from the RVC (n = 16) and the University of Bristol (n = 24) and whether these responses differed between dietary responders and non-responders. Here, plasma metabolites related to energy and amino acid metabolism significantly varied between CE and control cats in the RVC cohort. The hydrolyzed protein diet modulated the urinary metabolome of cats with CE (p = 0.005) in both the RVC and Bristol cohort. In the RVC cohort, the urinary excretion of phenylacetylglutamine, p-cresyl-sulfate, creatinine and taurine at diagnosis was predictive of dietary response (p = 0.025) although this was not observed in the Bristol cohort. Conversely, in the Bristol cohort plasma betaine, glycerol, glutamine and alanine at diagnosis was predictive of outcome (p = 0.001), but these same results were not observed in the RVC cohort. The biochemical signature of feline CE in the RVC cohort was consistent with that identified in human and animal models of inflammatory bowel disease. The hydrolyzed protein diet had the same effect on the urinary metabolome of cats with CE at both sites. However, biomarkers that were predictive of dietary response at diagnosis differed between the 2 sites. This may be due to differences in disease severity, disease heterogeneity, factors unrelated to the disease or small sample size at both sites. As such, further studies utilizing larger number of cats are needed to corroborate these findings.
引用
收藏
页数:12
相关论文
共 70 条
[1]   Modelling the role of microbial p-cresol in colorectal genotoxicity [J].
Al Hinai, Eiman Abdulla ;
Kullamethee, Piyarach ;
Rowland, Ian R. ;
Swann, Jonathan ;
Walton, Gemma E. ;
Commane, Daniel M. .
GUT MICROBES, 2019, 10 (03) :398-411
[2]   Conventional markers of kidney function [J].
Bagshaw, Sean M. ;
Gibney, R. T. Noel .
CRITICAL CARE MEDICINE, 2008, 36 (04) :S152-S158
[3]   Outcome of chronic inflammatory enteropathy in cats: 65 cases (2011-2021) [J].
Bandara, Y. ;
Priestnall, S. L. ;
Chang, Y. M. ;
Kathrani, A. .
JOURNAL OF SMALL ANIMAL PRACTICE, 2023, 64 (03) :121-129
[4]   1. Classification, risk factors, clinical signs and non-invasive diagnostics [J].
Barrs, Vanessa ;
Beatty, Julia .
JOURNAL OF FELINE MEDICINE AND SURGERY, 2012, 14 (03) :182-190
[5]   2. Further diagnostics, therapy and prognosis [J].
Barrs, Vanessa ;
Beatty, Julia .
JOURNAL OF FELINE MEDICINE AND SURGERY, 2012, 14 (03) :191-201
[6]   Metabolomics as a Promising Resource Identifying Potential Biomarkers for Inflammatory Bowel Disease [J].
Bauset, Cristina ;
Gisbert-Ferrandiz, Laura ;
Cosin-Roger, Jesus .
JOURNAL OF CLINICAL MEDICINE, 2021, 10 (04) :1-25
[7]   The Metabonomic Signature of Celiac Disease [J].
Bertini, Ivano ;
Calalbro, Antonio ;
De Carli, Valeria ;
Luchinat, Claudio ;
Nepi, Stefano ;
Porfirio, Berardino ;
Renzi, Daniela ;
Saccenti, Edoardo ;
Tenori, Leonardo .
JOURNAL OF PROTEOME RESEARCH, 2009, 8 (01) :170-177
[8]   Microbiome-metabolome reveals the contribution of gut-kidney axis on kidney disease [J].
Chen, Yuan-Yuan ;
Chen, Dan-Qian ;
Chen, Lin ;
Liu, Jing-Ru ;
Vaziri, Nosratola D. ;
Guo, Yan ;
Zhao, Ying-Yong .
JOURNAL OF TRANSLATIONAL MEDICINE, 2019, 17 (1)
[9]   Identification of intra- and inter-individual metabolite variation in plasma metabolite profiles of cats and dogs [J].
Colyer, Alison ;
Gilham, Matthew S. ;
Kamlage, Beate ;
Rein, Dietrich ;
Allaway, David .
BRITISH JOURNAL OF NUTRITION, 2011, 106 :S146-S149
[10]   Serum and urine metabolomic fingerprinting in diagnostics of inflammatory bowel diseases [J].
Dawiskiba, Tomasz ;
Deja, Stanislaw ;
Mulak, Agata ;
Zabek, Adam ;
Jawien, Ewa ;
Pawelka, Dorota ;
Banasik, Miroslaw ;
Mastalerz-Migas, Agnieszka ;
Balcerzak, Waldemar ;
Kaliszewski, Krzysztof ;
Skora, Jan ;
Barc, Piotr ;
Korta, Krzysztof ;
Pormanczuk, Kornel ;
Szyber, Przemyslaw ;
Litarski, Adam ;
Mlynarz, Piotr .
WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (01) :163-174