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Does
Stimulant Treatment for ADHD Increase Risk of Drug Abuse?
06/18/07
Researchers say treatment
age and duration can influence outcome; urge further study
Panayotis
(Peter) Thanos
Brookhaven
Researcher
Credit:
Brookhaven Nat. Labs.
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Parents, doctors, and
others have wondered whether common treatments for
attention-deficit hyperactivity disorder (ADHD) inadvertently
predispose adolescents to future drug abuse. The answer may
depend on the age at which treatment is started and how long it
lasts, say the authors of a new brain-imaging and behavioral
study conducted in animals at the U.S. Department of Energy's
Brookhaven National Laboratory. The results appear in the June 5,
2007 online issue of the journal Pharmacology, Biochemistry and
Behavior.
"Our study shows that the
brain's reward pathways are definitely influenced by
methylphenidate, one of the stimulant drugs commonly used to
treat ADHD," said Brookhaven researcher Panayotis (Peter)
Thanos, lead author of the study. "But the brain chemistry
changes we observed suggest that the developmental stage at which
treatment begins and the duration of treatment are important
variables that need further study."
In the study, rats were given
methylphenidate mixed with distilled water beginning one month
after birth -- early adolescence for rats. Animals received
either 1 or 2 milligrams methylphenidate per kilogram of body
weight, consistent with clinical doses given to children with
ADHD. A control group of rats was handled under identical
conditions but given plain water.
After two months of treatment,
and again after eight months, the scientists performed positron
emission tomography (PET) scans to measure the levels of dopamine
D2 receptors, a type of brain receptor important for experiencing
reward and pleasure that has been linked to pleasure and drug
abuse. After the eight-month treatment, animals were also tested
for their propensity to self-administer cocaine.
Rats given the 2mg/kg dose of
methylphenidate were significantly less likely to press a lever
to self-administer cocaine, and received fewer self-initiated
infusions of the drug following eight months of treatment than
the lower-dose group or the control rats.
The changes observed in brain
chemistry were specific to the age and duration of
methylphenidate treatment: Specifically, after two months of
treatment, brain scans revealed that both groups of treated rats
had lower levels of dopamine D2 receptors in their brains than
did control animals.
In contrast, after eight months
of treatment, the brain scans revealed elevated levels of
dopamine D2 receptors in treated rats compared with controls,
with the higher-dose treatment group showing the highest level of
D2 receptors. In the control group, D2 receptor levels declined
with age. Research at Brookhaven and elsewhere has suggested that
low levels of dopamine D2 receptors may increase the likelihood
of drug abuse, while elevated levels of dopamine D2 receptors may
attenuate the propensity to abuse drugs.
"This new study provides
evidence that chronic methylphenidate treatment begun in
adolescence affects the brain's dopamine D2 receptor levels, and
thus the brain's reward circuitry, differently depending on the
age and treatment duration," Thanos said. The scientists'
observation of lower rates of cocaine self-administration in the
animals treated for eight months with a 2kg/mg dose of
methylphenidate supports this idea.
However, the observation of
lower levels of D2 receptors after two months of treatment
suggests that shorter lengths of treatment or the age at which
treatment is evaluated could result in different effects. "Lower
dopamine D2 receptor levels following short-term treatment could
make the animals more vulnerable to drug self-administration
during early adulthood," Thanos said. "Unfortunately,
we cannot compare cocaine self-administration following eight
months of treatment with that obtained after two months of
treatment in the same animals, since animals were not tested for
cocaine self-administration at this earlier time," Thanos
said. "We wanted to avoid any confounding effect that might
have resulted from cocaine exposure during this early
developmental stage," he explained.
Evaluating the effect of
treatment duration is one avenue the researchers are exploring in
follow-up studies "to help assess optimal duration of
treatment regimes to minimize adverse effects on the propensity
to abuse drugs," Thanos said.
Thanos notes that the findings
from this study cannot be directly extrapolated to treatment
regimes used for ADHD. Also, these studies were done in healthy
animals, not in rodent models of ADHD. All experiments were
conducted in conformity with the National Academy of Sciences
Guide for Care and Use of Laboratory Animals and Brookhaven
National Laboratory Institutional Animal Care and Use Committee
protocols.
This research was funded by the
National Institute on Alcohol Abuse and Alcoholism intramural
program and by the Office of Environmental and Biological
Research within the U.S. Department of Energy's Office of
Science.
Source:
Brookhaven National Laboratories

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