Narcolepsy is the
term given to a sleep disorder in which the brain is unable to regulate the
sleep cycle properly. The patient will suffer from excessive daytime sleep or
even sudden bouts of nap.
Narcolepsy is
believed to have strong connections with misguided immune attacks, and is
therefore suspected of being an autoimmune disease. Patients suffering from Narcolepsy are also
at the risk of sleep-paralysis, insomnia, hallucinations or even cataplexy.
Cataplexy
is a condition in which the person suffers from sudden spells of muscle
weakness. It is the most common symptom of narcolepsy according to the U.S. National Institute of Neurological
Disorders and Stroke, and afflicts more than 3,000 people in the
United States alone.
Fortunately,
research has laid out the possibility of a treatment focusing on the immune
system that could be used against the disease. One of the possible causes of
the disorder is decreased levels of hypocretin or orexin in the brain. The deficiency might result from
an
abnormal immune system that attacks on the brain cells that produce hypocretin.
One of
the feasible cures for Narcolepsy is the
use of T-cells to treat the sleep disorder with an immune-suppressing therapy.
T cells are a key part of immune system defenses against infection, and
researchers believe that narcolepsy patients have blood T cells that react to a
particular hyprocretin protein.
Bentham
Science Publishers’ subscription based journal, “CNS & Neurological
Disorders - Drug Targets” publishes research articles and reviews on the
medicinal chemistry, pharmacology, molecular biology, genomics and biochemistry
of contemporary molecular targets involved in neurological and central nervous
system (CNS) disorders e.g. disease specific proteins, receptors, enzymes,
genes. For more information on Narcolepsy, you can refer to one of the
articles in this journal: “The Hypocretins and their Role in Narcolepsy” (http://www.benthamscience.com/cdtcnsnd/contabs/cdtcnsnd8-4.htm#5).
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