Interaction Between Bifidobacterium and Medical Drugs View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2016

AUTHORS

Temitayo O. Obanla , Saeed A. Hayek , Rabin Gyawali , Salam A. Ibrahim

ABSTRACT

Probiotics are live microorganisms which when administered in adequate amounts confer beneficial health benefits to the host. However, commonly consumed medical drugs may interact with probiotic bacteria and influence their viability and functionality. The objective of this study was to determine the impact of commonly administered medical drugs on the survival of Bifidobacterium. Five strains of Bifidobacterium (B. breve, B. longum, B. infantis, B. adolescentis, and B. bifidium) were individually grown in MRS broth at 37 °C for next day use. One tablet of commonly used medical drug (Aleve, Aspirin, Tylenol, Hydro, Lisinopril, Metformin, Metoprolol, or Glipizide) was completely dissolved into batches of 9 mL MRS broth then samples were inoculated with 1 mL of overnight grown cultures. Samples were incubated at 37 °C for 2 h and bacterial populations were determined immediately after exposure to medical drugs and after 2 h of incubation. Our result showed a decrease in bifidobacteria population by an average of 3.0 ± 0.25 log CFU/mL in the presence of tested drugs. Arthritis drug (Aleve, Aspirin, and Tylenol) showed higher killing effect on bifidobacteria compared to other tested drugs. These findings suggested that intake of common medical drugs may decrease the viability of probiotic bacteria and may reflect their contribution to human health. The intake of probiotic dietary supplements and functional foods may reduce the negative effect of medical drugs on probiotics. More... »

PAGES

171-178

Book

TITLE

Proceedings of the 2013 National Conference on Advances in Environmental Science and Technology

ISBN

978-3-319-19922-1
978-3-319-19923-8

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-3-319-19923-8_17

DOI

http://dx.doi.org/10.1007/978-3-319-19923-8_17

DIMENSIONS

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