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PMID: 16092071 Published · ppublish English Comparative Study Journal Article Review

Broad spectrum anti-infective potential of xanthohumol from hop (Humulus lupulus L.) in comparison with activities of other hop constituents and xanthohumol metabolites.

Molecular nutrition & food research ·Vol. 49 ·No. 9 ·2005-09-00 ·Pages 827-31

Gerhäuser C

Abstract

This review summarizes the capacity of xanthohumol (XN) in comparison with additional hop constituents and metabolites to act as an antiinfective agent against microorganisms including bacteria, viruses, fungi and malarial protozoa. XN was shown to inhibit the Gram-positive bacteria Staphylococcus aureus and Streptococcus mutans. Antiviral activity was demonstrated against bovine viral diarrhea virus, cytomegalovirus, herpes simplex virus type 1 and 2 and human immunodeficiency virus 1. Inhibition of two Trichophyton spp. was indicative of antifungal activity. Finally, XN potently inhibited the replication of Plasmodium falciparum, the causative agent of malaria. This effect was linked to the inhibition of glutathione-mediated degradation and detoxification of haemin, a by-product of the parasitic digestion of haemoglobin. Overall, these activities further contribute to the broad spectrum of biological effects observed with XN.

MeSH Terms
Animals Anti-Infective Agents/pharmacology Bacteria/drug effects Flavonoids Fungi/drug effects Humans Humulus/chemistry Malaria/prevention & control Molecular Structure Plasmodium falciparum/drug effects Propiophenones/chemistry,metabolism,pharmacology Viruses/drug effects
Chemicals
Anti-Infective Agents Flavonoids Propiophenones xanthohumol
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Gerhäuser Clarissa
Division of Toxicology and Cancer Risk Factors, German Cancer Research Center, Heidelberg, Germany. c.gerhauser@dkfz.de
Article Info
Journal
Molecular nutrition & food research
Abbr.
Mol Nutr Food Res
ISSN
1613-4125
Published
2005-09-00
Pages
827-31
Language
English
Region
Germany
NLM ID
101231818
Subset
IM
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