Scientists were working on the previous hypothesis that early meth abuse can cause the same symptoms as those experienced by Parkinson's disease patients who are missing a key protein, said the findings in the journal Neuroscience.
For the study, researchers gave two groups of young mice either methamphetamine or saline injections four times over an eight-hour period.
One group of mice was normal, the other had a partial depletion of glial derived neurotrophic factor (GDNF), a protein that protects and repairs dopamine, an important neurotransmitter, in areas of the brain related to motor control.
Loss of nerve cells that produce dopamine is a major contributor to Parkinson's disease.
The mice were 2.5 months old, or adolescents, at the start of the study. At 12 months old, the GDNF-depleted mice moved significantly less than the normal mice that got the same meth injections, according to the study.
Additionally, the immediate effects of the meth binge were exacerbated in the mice with the GDNF depletion.
"These studies speak directly to the possibility of long-term public health consequences resulting from the current epidemic of methamphetamine abuse among young adults," said Jacqueline McGinty, researcher at the Medical University of South Carolina, who led the study.
The study was funded by the US Army and National Institutes of Health.
Meth, also called speed, crystal or ice, is a highly addictive stimulant that increases wakefulness and suppresses appetite. It can be taken as a pill, smoked, snorted or injected. Long-term use can lead to hallucinations and stroke.
Nearly 12 million Americans have tried meth, according to a 2004 federal survey on drug use. Among teens, 6.2 percent of 17- and 18-year-olds in the United States said they have tried meth at least once.