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Ecstasy
José Gerardo Cruz Rivera
Abstract:
______________________________________________________________________________
MDMA can induce euphoria, a sense of intimacy with others, and diminished anxiety and
depression. Many, particularly in the fields of psychology and cognitive therapy, have suggested
MDMA might have therapeutic benefits and facilitate therapy sessions in certain individuals, a
practice which it had formally been used for in the past. Clinical trials are now testing the
therapeutic potential of MDMA forpost-traumatic stress disorder (PTSD) and anxiety associated
with terminal cancer. The subjective effects, side effects, short term effects and long term effect
of ecstasy are important for the people who use it.
Introduction
MDMA
(methylenedioxymethamphetamine) or
ecstasy is a dangerous substance that has
become a problem in society due to
overuse. Ecstasy is a dangerous drug that
should never be taken under any
circumstances, but now scientists have done
research on the help that this substance does
in humans.
Ecstasy is in fact a synthetic
methamphetamine derivative related to both
Amphetamine and Mescaline. Ecstasy is
widely used at such teen events as dance
club or “rave” parties, like techno parties,
but are not exclusive to those events.
Ecstasy was first synthesized in 1912 by
Merck, a German company, to be used as an
appetite suppressant or a weight-loss drug.
Ecstasy produces both stimulant and
psychedelic effects, enabling those who take
the drug to remain active for longer periods
of time with less fatigue.
According to the Office of National
Drug Control Policy, in 2000 the among
high school students surveyed are, 8.2% of
12th graders, 5.4% of 10th graders, and
3.1% of 8th graders stated that they had used
Ecstasy in the past year. According to the
1999 National Household Survey on Drug
Abuse, approximately 3.4 million people
had reported having used Ecstasy at least
once in their life.
Ecstasy and oral health
According to Brand, The ecstasy is
frequently used by young adults in the major
cities. This describes systemic and oral
effects of ecstasy. Life-threatening
complications include hyperthermia,
hyponatraemia and liver failure. In addition,
psychotic episodes, depression, panic
disorders and impulsive behaviour have
been reported. Oral effects include
xerostomia, bruxism, and an increased risk
of developing dental erosion. This occurs
because the ecstasy stops the cardiovascular
system. Recent use of ecstasy may interfere
with dental treatment.
Subjective effects
The most common effect of MDMA
was a heightened sense of "closeness" with
other people (90% of subjects). Tachycardia,
dry mouth, bruxism and trismus were
reported by the majority of users. These
effects probably result from the
amphetaminelike properties of the drug.
Side effects
Many ecstasy side effects are similar
to those found with the use of cocaine and
amphetamines: confusion, depression, sleep
problems, drug craving, severe anxiety, and
paranoia, during and sometimes weeks after
taking Ecstasy. Physical Ecstasy side effects
brought on by use of the drug include
muscle tension, involuntary teeth clenching,
nausea, blurred vision, rapid eye movement,
faintness, and chills or sweating.
Short-terms effects
While Ecstasy is not as addictive as
heroin or cocaine, it can cause severe
adverse effects including nausea,
hallucinations, chills, sweating, increases in
body temperature, tremors, involuntary teeth
clenching, muscle cramping, and blurred
vision.
After effects
Ecstasy users also report after-effects
of anxiety, paranoia, and depression.
Long-Term Side Effects of Ecstasy In 1998, the National Institute of
Mental Health conducted a study of a small
group of habitual Ecstasy users who were
abstaining from use. The study revealed that
the abstinent Ecstasy users suffered damage
to the neurons in the brain that transmit
serotonin, an important biochemical
involved in a variety of critical functions
including learning, sleep, and integration of
emotion. The results of the study have
shown that recreational Ecstasy users may
be at risk of developing permanent brain
damage that may manifest itself in
depression, anxiety, memory loss, and other
neuropsychotic disorders.
Overdose Ecstasy
An Ecstasy overdose occurs when
more Ecstasy is consumed than your body
can safely handle.
As of November 1995, 50 to 60 people had
died due to either an ecstasy overdose or
dehydration because of Ecstasy. Ecstasy
overdoses persist currently, including 8
people in Miami and 5 in Minneapolis/St.
Paul. In Boston during the first three
quarters of 2000, Ecstasy was the most
frequently mentioned drug in telephone calls
to the Poison Control Center.
Warning Signs of Ecstasy Overdose Feeling hot or unwell
Becoming confused, not able to talk
properly
Headache
Vomiting
Not Sweating
Racing heart or pulse when resting
Fainting or collapsing Loss of control over body movements
Tremors
Problems Urinating
An Ecstasy Overdose is characterized by: rapid heartbeat
high blood pressure
faintness
muscle cramping
panic attacks
loss of consciousness
seizures
hypothermia
muscle breakdown
stroke
kidney and cardiovascular system
failure
permanent damage to sections of
brain critical to thought and memory
death
MDMA (Ecstasy)-Assisted Psychotherapy
Relieves Treatment-Resistant PTSD
Belmont, MA-based Rick Doblin, Ph.D.,
President of the Multidisciplinary
Association for Psychedelic Studies (a non-
profit psychedelic and medical marijuana
research and educational organization that
sponsored the study), together with South
Carolina-based psychiatrist Michael
Mithoefer, MD and colleagues, made an
investigation on 20 patients with an average
of 19 years with chronic post-traumatic
stress disorder. Prior to enrolling in the
MDMA study, subjects were required to
have received, and failed to obtain relief,
from both psychotherapy and
psychopharmacology.
They analyzed these patients with MDMA
and placebo. Participants treated with a
combination of MDMA and psychotherapy
was statistically and clinically significant
improvements more than the placebo group
in post-traumatic stress disorder.
The trial focused on psychotherapy sessions
of eight hours scheduled about 3-5 weeks
apart, where 12 subjects received MDMA,
and eight took a placebo. Subjects also were
given psychotherapy once a week, before
and after each experimental session. An
evaluator-blind, independent tested each
subject using a scale of PTSD at baseline
and at intervals of four days after each
session and two months after the second
session. The clinical response was
significant - 10 of 12 in the treatment group
responded to treatment compared with only
two of eight in the placebo group. During
the trial, subjects had no drug related serious
adverse events (SAEs) or adverse
neurocognitive effects or clinically
significant blood pressure or temperature
increase Conclusion
Although MDMA could induce emotional
openness, which is an invaluable tool in
psychoanalysis, it poses a risk of flashbacks in
victims of rape, child abuse, or posttraumatic
stress disorder that could create suicidal
ideations in these patients.
Further research needs to be conducted to
explore whether the long-term cognitive and
memory deficits are permanent or partially or
fully reversible, and to elucidate the mechanism
of action and dosage of SSRIs in blocking the
action of Ecstasy. The latter may be promising
for the administration of SSRIs in managing
Ecstasy dependence and associated neuron
degeneration.
Recognizing the elevated abuse ( 500% increase
since 1994) and toxic of Ecstasy, the DEA has
substantially increased its operations against
Ecstasy trafficking and smuggling, mainly from
Western Europe. The DEA also has been active
in cleaning up drug use at rave parties.
It may be time to increase educational efforts
directed toward young adolescents and their
parents about the detrimental effects of Ecstasy.
Short-term as well as long-term dangers should
be emphasized. Finally, further clinical research
on the effects of MDMA is needed to provide
answers to important questions that remain.
Refereces
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[internet]. [cited 2010 Nov24]. Available
from: http://www.narconon.ca/Ecstasy.htm
-Brand H. S. Dun S. N. and Nieuw
Amerongen, A. V. 2008. Ecstasy (MDMA)
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MDMA (Ecstasy). [internet]. [cited 2010
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http://drugabuse.gov/infofacts/ecstasy.html
-SAGE Publications UK (2010, July 20).
MDMA (Ecstasy)-assisted psychotherapy
relieves treatment-resistant PTSD, study
suggests.ScienceDaily. Retrieved October
21, 2010, from:
http://www.sciencedaily.com/releases/2010/
07/100719082927.htm
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Overview of ecstasy (MDMA, MDA)
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