Coffee, Beyond Caffeine

Coffee—caffeinated or decaffeinated—protects liver and gastrointestinal cells from toxic compounds, according to Sandra Kalthoff et al. in the November issue of Gastroenterology.

In many epidemiology studies, coffee consumption reduced the risk of inflammation, chronic liver diseases, hepatocellular carcinoma (HCC), and other GI disorders. Its mechanisms are unclear, however, because coffee contains many complex compounds. Studies have shown that caffeine increases intracellular cAMP levels and disrupts TGF-ß signaling, whereas the coffee oils cafestol and kahweaol inhibit binding of aflatoxin B to DNA, induce glutathione-S-transferase, and protect against genotoxicity.

Kalthoff et al. add to the list of coffee’s super-powers, reporting that coffee increases production of UDP-glucuronosyltransferases (UGT1A )—enzymes with antioxidant, cytoprotective and genoprotective effects that mediate detoxification in the liver.

The authors discovered this effect after incubating liver, colon, and esophageal cells with different types of coffee (metal- and paper-filtered, boiled, decaffeinated, and instant) and related drinks (green and black tea and cocoa); paper-filtered coffee contains less cafestol and kahweaol, decaffeinated coffee lacks caffeine, and tea contains caffeine but is not processed by roasting. All preparations, except for black tea, induced transcription of the family of UGT1A genes, which encode enzymes that catalyze the formation of glucuronides from carcinogens and reactive oxygen species. These effects also occurred in vivo—giving coffee to mice upregulated UGT1A 10-fold or more in liver and stomach. 

UGT1A induction was independent of caffeine, methylxanthines, cafestol, or kahweaol, so more studies are needed to find out what compound or combination of compounds are required to induce transcription. Nonetheless, Kalthoff et al. propose that coffee extracts might be used as chemoprotectants against HCC, chronic hepatitis, or other liver diseases in high-risk groups. 

Antioxidant capacity of tested beverages.

Read the article online:
Kalthoff  S, Ehmer U, Freibert N, et al.  Coffee induces expression of glucuronosyltransferases by the aryl hydrocarbon receptor and Nrf2 in liver and stomach. Gastroenterology 2010;139:1699–1710.e2.

Read the accompanying editorial:
Gressner OA.  In the search of the magic bullet…Gastroenterology 2010;139:1453–1457.

About these ads

About Kristine Novak, PhD, Science Editor

Dr. Kristine Novak is the science editor for Gastroenterology and Clinical Gastroenterology and Hepatology, both published by the American Gastroenterological Association. She has worked as an editor at biomedical research journals and as a science writer for more than 12 years, covering advances in gastroenterology, hepatology, cancer, immunology, biotechnology, molecular genetics, and clinical trials. She has a PhD in cell biology and an interest in all areas of medical research.
This entry was posted in Liver/Biliary and tagged , , . Bookmark the permalink.

2 Responses to Coffee, Beyond Caffeine

  1. Chip says:

    That was pretty interesting. I’m surprised that decaffeinated coffee is higher than regular caffeinated coffee. I’m not surprised by green tea. What is boiled coffee?

  2. Biljana says:

    What about coffe and stomac disseases?Grean and black tea are herbs.Can you explain more about coffe because it is plant too,and positive stimulation in enzims at GIT.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s