Researchers at Washington University School of Medicine in St. Louis have demonstrated a new approach to treating muscular dystrophy. Mice with a form of this muscle-weakening disease showed improved strength and heart function when treated with nanoparticles loaded with rapamycin, an immunosuppressive drug recently found to improve recycling of cellular waste.
The study appears online in The FASEB Journal.
The investigators, including first author Kristin P. Bibee, MD, PhD, looked at a mouse model of Duchenne muscular dystrophy, the most severe inherited form of the disease. Duchenne exclusively affects boys, who have to rely on wheelchairs by age 12 and die from heart or respiratory failure in their 20s.
The faulty gene that causes the disease prevents the body from producing dystrophin, a protein crucial for maintaining muscle cell integrity and function. The new study demonstrated that mice with muscular dystrophy, in addition to missing dystrophin, also can’t recycle cellular waste, a process known as autophagy, or self-eating.
“Autophagy plays a major role in disposing of cellular debris,” said senior author Samuel A. Wickline, MD, the James R. Hornsby Family Professor of Medicine. “If it doesn’t happen, you might say the cell chokes on its own refuse. In muscular dystrophy, defective autophagy is not necessarily a primary source of muscle weakness, but it clearly becomes a problem over time. If you solve that, you can help the situation by maintaining more normal cellular function.”
Although it’s not clear how the missing dystrophin protein might be responsible for the muscle cells’ poor housekeeping, the study showed that boosting autophagy improved skeletal muscle strength and heart function in these mice.
“Some investigators are looking for ways to replace dystrophin,” said co-author Conrad C. Weihl, MD, PhD, associate professor of neurology. “But here we are focusing on the defect in autophagy. What is exciting about our approach is that there are existing drugs that activate autophagy. And by repackaging the drug on nanoparticles, we can target it specifically to muscles and correct the defect in the cells’ ability to recycle waste.”
Shown is a diaphragm muscle of a mouse with muscular dystrophy (top). Pictured below are fluorescent nanoparticles (red) lodged in the diaphragm.
When treated with rapamycin nanoparticles, the mice showed a 30 percent increase in grip strength and a significant improvement in cardiac function, based on an increase in the volume of blood the heart pumped.
“An important aspect of our study is that we are treating both skeletal muscle and heart muscle with the same drug,” Wickline said. “The heart is a difficult organ to treat in muscular dystrophy. But even in older animals, this regimen works well to recover heart function, and it is effective over a short period of time and after only a few doses.”
“Death from Duchenne in many people is due to heart dysfunction,” said Weihl, who also treats patients with neuromuscular disorders at Barnes-Jewish Hospital. “So even improving cardiac function by 10 percent in late-stage disease could be very important.”
The nanoparticle used in the study consists of an inert core made of perfluorocarbon, originally designed as a blood substitute. The particles are about 200 nanometers in diameter — 500 times smaller than the thickness of a human hair. The surface of the nanoparticle is coated with rapamycin, which suppresses the immune system. The drug typically is used to help prevent organ rejection in transplant patients. It is known for its anti-inflammatory properties and, more recently, for its role in activating autophagy.
When injected into the bloodstream, according to Wickline, the nanoparticles accumulate in areas of inflammation, where damaged tissues have leaky blood vessels and are undergoing cell death and repair.
“The nanoparticles tend to penetrate and be retained in areas of inflammation,” Wickline said. “Then they release the rapamycin over a period of time, so the drug itself can permeate the muscle tissue.”
Compared with oral delivery, the nanoparticle approach also allowed the researchers to give the mice smaller doses of the drug.
“We showed that oral doses of rapamycin, even at 10 times the dose we used in the nanoparticles, were ineffective,” Weihl said. “This is important because rapamycin suppresses the immune system, and directly targeting it to muscle in smaller doses would reduce unwanted side effects.”
Current treatment for Duchenne involves corticosteroids such as prednisone, which has been shown to extend the time patients are able to walk. But steroids also cause weight gain, brittle bones, high blood pressure and other long-term side effects.
Although it’s not clear why steroid treatment helps maintain skeletal muscle strength, Weihl said the study suggests prednisone also may promote autophagy, raising the possibility of combination therapy, in which both steroid treatment and rapamycin nanoparticles could be given simultaneously, each at lower doses.
This work was supported by the National Institutes of Health (NIH) grants R01 AR056223, HL073646, HL112518, HL113392, NS073457ß, K02 AG042095, the Muscular Dystrophy Association, and the American Heart Association.
Bibee KP, Cheng YJ, Ching JK, Marsh JN, Li AJ, Keeling RM, Connolly AM, Golumbek PT, Myerson JW, Hu G, Chen J, Shannon WD, Lanza GM, Weihl CC, Wickline SA. Rapamycin nanoparticles target defective autophagy in muscular dystrophy to enhance both strength and cardiac function. The FASEB Journal. Online Feb. 5, 2013.
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