Brain Chemistry
A peptide is a chain of amino acids joined together by peptide
bonds. Many peptides produced by cells of the brain serve as neurotransmitters,
neuromodulators or hormones. Proteins are long peptides.
Oxytocin
Oxytocin is a neuropeptide that is involved in social functions
such as attachment and bonding. Oxytocin receptor fields are labile
(there are shifts in receptor density occurring in early development).
A failure to shift from an infantile to a mature pattern may underlie
autism. 30 autistic children were found to have lowered levels
of plasma oxytocin in comparison to normals. This leads to the
possibility that exposure to exogenous oxytocin (petocin) at time
of delivery (in patients who are genetically susceptible) may
cross the placenta and blood brain barrier and cause down regulation
of oxytocin receptors in the brain of the fetus, or even cause
and immune response to oxytocin receptors.
Vasoactive Intestinal Peptide, Calcitonin-related gene peptide,
Brain-derived neurotrophic factor and Neurotrophin 4
Elevated Levels of Neuropeptides/Neurotrophins
in Youngsters with Autism |
| Population |
Percent with
Elevated Neuropeptides & Neurotrophins |
| Autism |
96.9% |
| Mental Retardation |
92.4% |
| Cerebral Palsy |
9.2% |
| Healthy Children (Controls) |
0 |
- Most children diagnosed with Autism or Mental Retardation
had concentrations of 2 of more of the measured neuropeptides
or neurotrophins in peripheral blood at birth, while only few
children with CP and no control child did.
- Neuropeptides and neurotrophins measured include vasoactive
intestinal peptide, calcitonin related gene peptide, brain derived
neurotrophic factor, and neurtrophin 4.
In April 2000, scientists (Dr. Karin Nelson, National Institute
of Neurological Disorders and Stroke) discovered what they believe
may be biological markers in the blood of newborn infants who
later develop autism and mental retardation.
In their study, eight proteins were targeted that play a role
in the development of the brain. Blood samples (which were drawn
at birth and saved by the California Birth Defects Monitoring
Program) for healthy children as well as children who had later
been diagnosed with autism, mental retardation and cerebral palsy
were studied.
The study showed that most children with autism or mental retardation
had exceedingly high concentrations of 2 or more or the measured
neuropeptides or neurotrophins in their blood during the earliest
days of life while few of the cerebral palsy and none of the healthy
children did.
This study implies that a genetic component to autism and mental
retardation exists and that it may be possible to devise a test
which would allow identification of these markers at birth. If
we become able to identify children who have these high concentrations
of proteins at birth, we may consider them high risk and therefore
protect them from environmental factors which may exacerbate the
condition resulting in autism.
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