Printer Friendly
The Free Library
14,716,107 articles and books
Member login
User name  
Password 
 
Join us Forgot password?

Supplement could fight cystic fibrosis.


Preliminary studies in mice suggest that a common dietary supplement might ward off the debilitating de·bil·i·tat·ing
adj.
Causing a loss of strength or energy.


Debilitating
Weakening, or reducing the strength of.

Mentioned in: Stress Reduction
 effects of cystic fibrosis cystic fibrosis (sĭs`tĭk fībrō`sĭs), inherited disorder of the exocrine glands (see gland), affecting children and young people; median survival is 25 years in females and 30 years in males. , a genetic disease marked by life-threatening accumulations of mucus in the lungs.

Using mice carrying the genetic defect that causes the disease in people, Boston researchers showed that cell membranes in the lungs, pancreas, and intestines--the organs most affected by cystic fibrosis in people--have abnormally low levels of a fatty acid fatty acid, any of the organic carboxylic acids present in fats and oils as esters of glycerol. Molecular weights of fatty acids vary over a wide range. The carbon skeleton of any fatty acid is unbranched. Some fatty acids are saturated, i.e.  called docosahexaenoic acid docosahexaenoic acid /do·co·sa·hexa·eno·ic ac·id/ (do-ko?sah-hek?sah-e-no´ik) an omega-3, polyunsaturated, 22-carbon fatty acid found almost exclusively in fish and marine animal oils.  (DHA DHA docosahexaenoic acid.
DHA,
n.pr See acid, docosahexaenoic.
). Feeding the mice large doses of DHA for a week not only corrected the imbalance but also reversed signs of the disease, Juan G. Alvarez and his colleagues at Beth Israel Deaconess Medical Center Both an international and regional referral center, Beth Israel Deaconess Medical Center (BIDMC) in Boston, Massachusetts is a major teaching hospital of Harvard Medical School. It was formed out of the 1996 merger of Beth Israel Hospital (founded in 1916) and  reported in Seattle last month at the Cystic Fibrosis Foundation's annual meeting.

To examine the human respiratory and digestive tracts, the researchers took nasal and rectal samples. Their preliminary evidence shows lower DHA concentrations in cells of the six people with the disease than in those of six healthy volunteers.

Trials in which people with cystic fibrosis will receive DHA as a dietary supplement are slated to begin as early as next year. Meanwhile, researchers are warning people with cystic fibrosis not to start taking supplements, such as fish oil, that are rich in DHA. Other components of the supplements might harm people with the disease, say the researchers.

DHA caused no obvious side effects in the mice. "So, the treatment should be sale in humans, but we don't know that for sure," cautions Steven D. Freedman of Beth Israel.

Decreases in DHA concentration in cell membranes tend to translate into increases in a fatty acid called arachidonic acid. This compound promotes inflammation and immune responses, reactions that are overactive o·ver·ac·tive  
adj.
Active to an excessive or abnormal degree: an overactive child.



o
 in people with cystic fibrosis. The researchers propose that the imbalance between these two compounds is the source of characteristic symptoms such as chronic lung inflammation and excess mucus.

Unlike most cystic fibrosis drugs under development, DHA could be taken orally to treat disease symptoms throughout the body, not just in the lungs.
COPYRIGHT 1999 Science Service, Inc.
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 1999, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

 Reader Opinion

Title:

Comment:



 

Article Details
Printer friendly Cite/link Email Feedback
Author:D.C.
Publication:Science News
Article Type:Brief Article
Geographic Code:1USA
Date:Nov 6, 1999
Words:331
Previous Article:A lead on why lead hurts the brain.(Brief Article)
Next Article:Clogged arteries block hormone effects.(Brief Article)
Topics:



Related Articles
Cystic fibrosis flaw reversed in vitro.
Enzyme dissolves cystic fibrosis phlegm. (DNase I) (Brief Article)
Gene therapy for cystic fibrosis patients.
Gene therapy: a new Rx for CF? (experimental cystic fibrosis treatment)
Cystic fibrosis: an antibiotic cure? (aminoglycoside antibiotics overcome stop mutation in cystic fibrosis CTFR genes in 5% of...
Cystic fibrosis controversy: a new theory hints that gene therapy in the womb can cure disease. (research with mice)
Fibrosing colonopathy in an adult cystic fibrosis patient after discontinuing pancreatic enzyme therapy.(Case Report)
Vocational attainment of adults with CF: success in the face of adversity.(Cystic Fibrosis)
The challenge of nontuberculous mycobacteria in patients with cystic fibrosis.(Editorial)

Terms of use | Copyright © 2009 Farlex, Inc. | Feedback | For webmasters | Submit articles