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How does the body function
The body functions through biochemistry and chemical signaling.
Hormones, neurotransmitters, and other biochemical molecules regulate cognition, memory, sleep, and higher-order functions.
How do many mental illnesses start?
from chemical imbalances in the brain
Brain
The brain controls both autonomous (unconscious) and voluntary (conscious) functions.
It regulates behavior, self-control, sleep, and emotions.
Some behaviors are controllable, while others (e.g., OCD) are compulsive and harder to regulate.
Genetics and Personality
Genetics influence mental health and personality traits.
Different neurotransmitter balances contribute to different personalities.
Genome sequencing helps identify susceptibility to mental illnesses like Alzheimer's and Parkinson’s.
Historical Perspectives on Mental Health
In the past, mental illnesses were attributed to supernatural causes (e.g., demons).
Early treatments included trepanation (drilling holes in the skull), lobotomies, and electroshock therapy.
Development of Psychiatric Medications
1950s saw the emergence of effective psychiatric drugs.
Schizophrenia involves loss of reality, hallucinations, paranoia, and anxiety.
Early treatments included antihistamines (e.g., Promethazine, Thorazine), which helped calm patients but did not fully address all symptoms.
Histamines (chemical messengers) play roles in both allergic responses and brain function (e.g., sleep-wake cycles).
Some psychiatric drugs induce sleep by blocking histamines, which can help with anxiety but not other symptoms of mental illness.
How do antidepressants work?
Many antidepressants work by preventing the reuptake of neurotransmitters (e.g., serotonin, norepinephrine, dopamine) in the synaptic cleft, increasing their availability and enhancing mood.
Monoamine Oxidase Inhibitors
Monoamine Oxidase (MAO) is an enzyme that breaks down neurotransmitters like serotonin.
MAOIs inhibit this enzyme, leading to higher serotonin levels and mood enhancement.
However, early MAOIs caused serious side effects, such as liver toxicity (hepatotoxicity), leading to their discontinuation in favor of safer drugs.
TCAs
were early antidepressants that worked by blocking serotonin and norepinephrine reuptake.
They were effective but had major side effects, including:
Drowsiness (due to histamine receptor antagonism).
Dry mouth and memory issues (due to acetylcholine receptor antagonism).
Cardiovascular risks, making them dangerous in overdose situations.
SSRIs (Selective Serotonin Reuptake Inhibitors)
Specifically target serotonin reuptake without affecting histamine, dopamine, or acetylcholine systems.
Fewer side effects compared to TCAs and MAOIs.
Better safety profile, making them more suitable for long-term use.
Obsessive-Compulsive Disorder (OCD
OCD is linked to serotonin dysregulation, leading to compulsive behaviors, obsessive thoughts, and anxiety.
Symptoms include:
Ritualistic behaviors (e.g., repeatedly checking locks, excessive handwashing).
Perfectionism over minor details (e.g., aligning objects in a specific order).
SSRIs like Prozac are commonly used to increase serotonin levels and alleviate OCD symptoms.
Newer MAO inhibitors also show promise in treating OCD.
Bipolar Disorder and Chemical Imbalance
Bipolar disorder causes extreme mood swings, with alternating manic (high-energy) and depressive (low-energy) episodes.
Early theories (e.g., John Cade’s toxin hypothesis) suggested that toxins in the blood caused manic episodes.
Today, research points to neurotransmitter dysregulation, particularly involving serotonin, dopamine, and norepinephrine.
Lithium is the primary treatment, helping stabilize mood by modulating neurotransmitter activity.
Anxiety Disorders & Treatments
Related to increased adrenergic (adrenaline) response.
Barbiturates (discovered in 1864) were found to have anti-anxiety effects.
Barbiturates target GABA receptors, reducing neuronal activity (anxiolytic & hypnotic).Benzodiazepines (e.g., Valium, Xanax) replaced barbiturates as a safer alternative.
Benzodiazepines amplify GABA signaling by increasing receptor sensitivity.
Psychiatric Medications & Challenges:
Psychiatric drugs (e.g., Prozac, Valium) alter neurotransmission.
Critics argue they lack precise control over brain chemistry, leading to side effects.
Placebo effect plays a significant role in drug efficacy, influencing patient response.
Some psychiatric drugs are highly addictive and cause withdrawal symptoms.
Placebo Effect in Clinical Trials:
Placebos (sugar pills) are used as a control to measure drug effectiveness.
Placebo responses can mimic drug effects, making efficacy assessment complex.
Some individuals experience side effects from placebos (e.g., nausea, headaches, rashes).
Limitations in Psychiatric Drug Development:
Progress in psychiatric drugs has been slow compared to other fields like computing.
Most new drugs are minor modifications of older ones, reducing side effects but offering little improvement in efficacy.
The brain's extreme complexity makes developing precise treatments challenging.
The brain contains over 90 billion neurons and trillions of synapses, making targeted drug development difficult.