About My Health Careers Internship MedBlogs Contact us

Transplant Anti-Rejection Drug Benefits Mice With Leigh Syndrome

by Dr. Enozia Vakil on November 16, 2013 at 2:42 PM
Font : A-A+

 Transplant Anti-Rejection Drug Benefits Mice With Leigh Syndrome

Rapamycin-a transplant anti-rejection drug actually demonstrated benefits in a mouse having a fatal defect in the mitochondria. Children with the condition, Leigh syndrome, show progressive brain damage, muscle weakness, lack of coordination or muscle control, and weight loss, and usually succumb to respiratory failure.

Leigh syndrome is often diagnosed within the first year of life. Affected children rarely survive beyond 6 or 7 years. At present, the disorder, which can result from several different underlying causes, has no effective treatment.


Reporting this week in Science Express, University of Washington researchers said that they found that treatment with rapamycin "robustly enhances survival and attenuates disease progression in a mouse model of Leigh's syndrome." Given as a daily injection, the drug delayed the onset of neurological symptoms, reduced brain inflammation, and prevented brain lesions.

For most of their lives, the treated mice breathed normally, and did not clasp their legs against their bodies, a posture characteristic of this and related brain disorders in mice. Unlike the untreated mice, they could balance and run on a rotarod, a miniature log rolling exercise toy. Both the median and maximum lifespans within the group of treated mice were strikingly extended, the authors noted.

The median lifespan for this mouse condition is 50 days. In comparison, treated males lived a median of 114 days, and females 111 days. The longest survival in the treated group was 269 days, more than triple that of the untreated animals.

"We were excited at the findings because of the potential impact on treatment for kids with this or related mitochondrial diseases," said the senior author of the study, Dr. Matt Kaeberlein, associate professor of pathology at the University of Washington. "Similar intervention strategies might also prove useful for a broad range of mitochondrial diseases or for other conditions resulting from mitochondrial dysfunction."

Mitochondrial defects lessen the amount of energy available to cells. The depletion can damage or destroy vital tissues. Symptoms and severity of illness depends on which types of cells are affected, but in many cases several organ systems operate poorly as a consequence of malfunctioning mitochondria.

Beyond specific mitochondrial diseases, most of them genetic in origin, the decline or dysfunction of mitochondria also contribute to many common health problems, including some forms of heart disease, cancer, and muscle, nerve or brain degeneration associated with aging.

Kaeberlein, whose research focus has been factors that lengthen life, has been studying the anti-aging effects of rapamycin for several years. The drug, like calorie-restricting diets, acts by inhibiting mTOR, an abbreviation for the eponymously named mechanistic target of rapamycin.

Kaeberlein said, "This study suggests that this drug's inhibition of mTOR may have a major impact on mitochondria and energy production in cells. We also know that rapamycin appears to slow aging. What we don't know is whether the effects of rapamycin on mitochondria are a major part of the effects of rapamycin on normal aging and aging-related diseases."

Alongside their work in aging and lifespan in normal mice, Kaeberlein and his lab decided to study rapamycin's actions on mice with a severe mitochondrial defect. The mouse model for Leigh syndrome was created in the University of Washington laboratory of Dr. Richard Palmiter, a professor of biochemistry and Howard Hughes Medical Institute investigator who was one of the early originators of transgenic mouse models. The research team included Dr. Philip G. Morgan and Dr. Margaret M. Sedensky, from the Department of Anesthesiology and Pain Medicine at Seattle Children's Hospital, who study mitochondrial diseases in patients. The lead scientist was Simon C. Johnson from the UW Department of Pathology.

After seeing the unexpected benefits on health and survival, the research group looked more closely at the effects on metabolism by examining the levels of more than 100 different metabolites - cellular building blocks and intermediates used to make energy - in the treated and untreated Leigh syndrome mice. The team observed that the treated mice appear to be burning more amino acids and fats as an energy source, rather than the sugar, glucose. This eliminated the accumulation of glucose breakdown byproducts, including lactate. These byproducts can be toxic and are seen at high levels in human Leigh syndrome patients.

"The drug did not substantially alter mitochondrial composition. Instead, the mice appear to be bypassing the deficiency in their mitochondria through a shift in their metabolic pattern," Kaeberlein said. "However, we can't yet explain exactly how this rescues the mice with Leigh syndrome."

Because this was a mouse study, evidence ofefficacy of rapamycin in Leigh syndrome patients will be a necessary next step. Rapamycin already has FDA approval for several uses, including preventing organ transplant rejection and for treating rare forms of cancer; however, the drug also has side-effects which might limit its utility in very young children. Kaeberlein is optimistic, however, that "even if rapamycin doesn't turn out to be be useful as a treatment for Leigh Syndrome, the lessons learned here will pave the way to new therapies for this devastating disease."

Source: Eurekalert

News A-Z
News Category
What's New on Medindia
Woman with Rare Spinal Cord Defect from Birth Sues Doctor
World AIDS Day 2021 - End Inequalities, End AIDS
View all

Medindia Newsletters Subscribe to our Free Newsletters!
Terms & Conditions and Privacy Policy.

More News on:
Drug Toxicity Signature Drug Toxicity 

Recommended Reading
Researchers Uncover Genetic Mutation in Leigh Syndrome
A genetic mutation underlying late-onset Leigh syndrome, a rare inherited metabolic disorder ......
Zebrafish may Be Helpful in Studying Mitochondrial Impairments in Humans
Researchers have discovered a new application for tropical and popular aquarium fish, Zebrafish - .....
Baby Joseph Returns Home
Baby Joseph Maraachli, a 14-month-old Canadian boy, whose health issue had sparked an international ...
Drug Toxicity
Drug toxicity is an adverse reaction of the body towards a drug that results as a side effect of a d...

Disclaimer - All information and content on this site are for information and educational purposes only. The information should not be used for either diagnosis or treatment or both for any health related problem or disease. Always seek the advice of a qualified physician for medical diagnosis and treatment. Full Disclaimer

© All Rights Reserved 1997 - 2021

This site uses cookies to deliver our services. By using our site, you acknowledge that you have read and understand our Cookie Policy, Privacy Policy, and our Terms of Use