A new evaluation system for drug–microbiota interactions

Author:

Liu Tian‐Hao123ORCID,Zhang Chen‐Yang34,Zhang Hang5,Jin Jing2,Li Xue6,Liang Shi‐Qiang5,Xue Yu‐Zheng3,Yuan Feng‐Lai4,Zhou Ya‐Hong6,Bian Xiu‐Wu12,Wei Hong1

Affiliation:

1. Yu‐Yue Pathology Scientific Research Center Chongqing China

2. Department of Pathology Army Medical University Chongqing China

3. Department of Gastroenterology Affiliated Hospital of Jiangnan University Wuxi Jiangsu China

4. Institute of Integrated traditional Chinese and Western Medicine Affiliated Hospital of Jiangnan University Wuxi China

5. College of Animal Science and Technology, College of Animal Medicine Huazhong Agricultural University Wuhan Hubei China

6. Wuxi Hospital Affiliated to Nanjing University of Chinese Medicine Wuxi Jiangsu China

Abstract

AbstractThe drug response phenotype is determined by a combination of genetic and environmental factors. The high clinical conversion failure rate of gene‐targeted drugs might be attributed to the lack of emphasis on environmental factors and the inherent individual variability in drug response (IVDR). Current evidence suggests that environmental variables, rather than the disease itself, are the primary determinants of both gut microbiota composition and drug metabolism. Additionally, individual differences in gut microbiota create a unique metabolic environment that influences the in vivo processes underlying drug absorption, distribution, metabolism, and excretion (ADME). Here, we discuss how gut microbiota, shaped by both genetic and environmental factors, affects the host's ADME microenvironment within a new evaluation system for drug–microbiota interactions. Furthermore, we propose a new top‐down research approach to investigate the intricate nature of drug–microbiota interactions in vivo. This approach utilizes germ‐free animal models, providing foundation for the development of a new evaluation system for drug–microbiota interactions.

Publisher

Wiley

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