BHAV 455 MODULE 3- Neurobiology and Neuronal Communication in Behavioral Health

The Relevance of Neurology to Behavioral Health Professionals

  • Context of the Lecture: This module focuses on neurology for behavioral health, also known as behavioral neurobiology, emphasizing the transition from structural anatomy to functional communication between neurons.

  • Applicability to Practice:

    • While structural anatomy (e.g., brain injuries) is critical for specialists in rehabilitation centers, helping professionals (case managers, counselors, psychotherapists, psychologists) are often more interested in neuronal communication.

    • Primary clinical presentations such as anxiety and depression are rarely attributed to structural visible damage like a "small hypothalamus" or a "tear in the amygdala."

    • Instead, these psychological phenotypes usually manifest from issues with neurotransmitters (brain chemistry) and electrical activity.

  • Diagnostic Exceptions: Structural issues may be relevant in cases involving specific impairments in memory, expressive/receptive communication, or impulse control.

  • The Subsurface Reality of Behavior: Every human action is underpinned by neurological processes:

    • Hunger: Neurons in the hypothalamus release messages indicating low energy.

    • Planning and Habit: The thought "I should eat breakfast for energy" involves the firing of neurons.

    • Motor Sequences: Reaching for coffee involves planning, intention, and action sequences mediated by neuronal communication.

    • Reward: The feeling of pleasure or happiness from a drink (e.g., coffee) is a result of neural reward pathways.

The Unit of Communication: The Neuron

  • Definition: Neurons are specialized nerve cells that receive, integrate (interpret), and transmit information.

  • Hardware vs. Software Analogy:

    • Human brains are not hardware running software; the hardware is the software.

    • The "human biocomputer" differs from standard computers because the biological structure (the brain) is dynamic and self-shaping.

  • Total Count: There are approximately 100×109100 \times 10^9 (100 billion) neurons in the human brain (some estimates suggest 86×10986 \times 10^9).

  • Primary Functional Types:

    • Sensory Neurons: Detect sensory and environmental stimuli.

    • Motor Neurons: Control, initiate, and manage movement.

    • Pyramidal Neurons: Located in the neocortex; essential for conscious thought, memory, and self-reflective thinking (metacognition).

    • Mirror Neurons: Specialized neurons that fire both when performing an action and when witnessing someone else perform that same action.

      • Social/Vicarious Learning: These allow individuals to learn from others' mistakes (e.g., a child seeing a sibling burn their hand on a stove).

      • Empathy and Compassion: They facilitate "attuning" to another's experience, creating a resonance where the observer feel what the other is feeling.

Neural Networks and Alliances

  • Formation: Neurons interact and form networks through selective communication based on shared goals and functionality.

  • Neural Alliances: These are like co-ops or alliances formed through experience and habit.

  • Examples:

    • Skill Acquisition: Once a neural network for riding a bike is established, the neurons fire together automatically, eliminating the need to relearn the skill.

    • Addiction and Triggers: Strong neural alliances can be formed for survival or via maladaptation. In addiction, environmental cues (the "clink of a glass") can trigger a network that leads to automatic motor sequences (drinking) before conscious thought occurs.

    • Trauma: Adverse Childhood Experiences (ACEs) and trauma lead to rapidly formed, powerful alliances dedicated to fight-or-flight survival responses.

Anatomy of a Neuron

  1. Dendrites: Short, branch-like structures that detect neurochemical signals from neighboring neurons.

  2. Cell Body (Soma): The "microprocessor" of the cell; it collects, integrates, and interprets information received by the dendrites. It contains the nucleus, DNA, and genetic material.

  3. Axon: A long fiber extending from the cell body that transmits electrical impulses (action potentials). They can range from millimeters to over a meter in length.

  4. Terminal Buttons (Synaptic Knobs): Located at the ends of axons; they form the synapses and release chemical signals.

  • Myelin Sheath: An insulatory material (fatty layer) that coats the axon.

    • Functions: Speeds up communication and prevents the signal from degrading as it travels.

    • Nodes of Ranvier: Microscopic gaps in the myelin sheath. Signals can "jump" across these gaps (saltatory conduction), further increasing speed.

    • Multiple Sclerosis (MS): A condition characterized by the breakdown of myelin, leading to inefficient or failed message transmission.

Glial Cells: The Support System

  • Prevalence: Glial cells make up approximately 90%90\,\% of the brain's cells, while neurons make up only 10%10\,\%.

  • Historical View: They were once thought to be simple "packing peanuts" used to hold neurons in place.

  • Current Understanding: They are active dynamic participants in the brain's environment.

    • Microglia: The brain's specialized immune system and "janitorial crew"; they repair damage and remove waste.

    • Oligodendrites: Specialized glia that produce the myelin sheath in the central nervous system.

    • Astrocytes: Star-shaped cells and the most abundant type of glia.

      • Regulate the chemical environment.

      • Form the blood-brain barrier.

      • Provide metabolic support (oxygen/energy) to neurons.

      • Signal Modulation: They wrap around synapses to "eavesdrop" on communication. They can amplify important signals ("pump up the volume") or mute others through calcium-based communication.

The Action Potential (Neural Firing)

  • Definition: A rapid electrical signal and brief change in voltage across a neuron's membrane driven by ion movement.

  • Resting State: The neuron maintains a charge of 70mV-70\,mV (millivolts).

    • There is a high concentration of Sodium (Na+Na^+) ions outside and Potassium (K+K^+) ions inside.

    • Sodium-Potassium Pump: Constantly works to maintain this equilibrium; requires a disproportionate amount of human energy (burning fuel) to keep the brain "ready."

  • Threshold: If a stimulus is strong enough, the neuron hits a threshold of 55mV-55\,mV.

  • Depolarization: Voltage-gated sodium channels open, allowing Na+Na^+ to rush in, making the cell interior more positive.

  • Peak: The membrane potential spikes to roughly +30mV+30\,mV.

  • Repolarization: Sodium channels close and potassium channels open, letting K+K^+ flow out to restore the negative charge.

  • Hyperpolarization: A brief period where the membrane becomes more negative than 70mV-70\,mV due to excess potassium outflow.

  • All-or-Nothing Principle: Once the threshold is met, the signal fires completely and then resets.

Synaptic Transmission

  • The Synaptic Cleft: Neurons do not touch. There is a microscopic nanometer-scale gap (the cleft) between the pre-synaptic and post-synaptic cells.

  • The Process:

    1. The electrical action potential reaches the terminal button.

    2. Neurotransmitters (chemicals) are released from vesicles (small storage sacs).

    3. Neurotransmitters float across the synaptic cleft.

    4. Lock and Key Analogy: Neurotransmitters bind to specific receptors on the post-synaptic dendrite. If they do not fit the specific "lock," no message is sent.

    5. The post-synaptic cell decides whether to pass the message on or terminate it.

  • Termination of Signal: Once the message is delivered, the cleft must be cleared to allow for future clarity:

    • Re-uptake: The pre-synaptic neuron reabsorbs the neurotransmitter for recycling. This conserves energy and prevents over-excitation.

    • Enzymatic Breakdown: Enzymes dissolve the neurotransmitters in the cleft.

The Role of Calcium in Neurobiology

  • The Second Messenger: While sodium and potassium create the electrical charge (the spark), calcium (Ca2+Ca^{2+}) triggers the cell to take action.

  • Mechanism: When the action potential hits the axon terminal, it opens Voltage-Gated Calcium Channels (VGCCs).

  • Neurotransmitter Release: The influx of calcium causes the vesicles to fuse with the cell membrane, allowing neurotransmitters to be released into the cleft.

  • Gene Expression: Calcium can activate CREB (cAMP response element binding proteins).

    • CREB acts as a master switch for long-term memory and neuronal survival.

    • It triggers the synthesis of new proteins to alter the brain's physical architecture.

Synaptic Plasticity and Learning

  • Neuroplasticity: The brain's ability to strengthen or weaken connections based on experience.

  • Long-Term Potentiation (LTP): The biological basis of memory.

    • When a synapse is frequently activated, a large amount of calcium enters.

    • This increases the number of receptors on the receiving neuron.

    • The connection becomes stronger and more efficient (e.g., forming a habit or a bias toward negative thinking).

Major Neurotransmitters

  • Acetylcholine (ACh): Motor control, learning, memory, sleeping, and dreaming.

  • Norepinephrine: Arousal, vigilance, and attention (linked to anxiety and trauma responses).

  • Serotonin: Emotional states, impulse control, and dreaming.

  • Dopamine: Reward, motivation, and motor control over voluntary movement.

  • GABA: Primary inhibitory neurotransmitter; helps with anxiety reduction and calming.

  • Glutamate: Primary excitatory neurotransmitter; crucial for memory formation.

  • Endorphins: Pain reduction and neural reward.

Neuropharmacology in Behavioral Health

  • Agonists: Substances that enhance a neurotransmitter's effect.

    • They can mimic the neurotransmitter (e.g., Heroin mimics natural pain-relieving chemicals).

    • They can increase the manufacturing or release of the chemical.

    • They can block re-uptake.

  • Antagonists: Substances that inhibit a neurotransmitter's effect.

    • They can block receptors so the real neurotransmitter cannot lock in.

    • They can destroy neurotransmitters in the synapse or decrease their production.

    • Example: Botox is an antagonist that inhibits the release of Acetylcholine, preventing muscle contraction.

  • SSRIs (Selective Serotonin Re-uptake Inhibitors):

    • Popular pharmacological interventions for depression/anxiety.

    • Rationale: They inhibit the re-uptake process, leaving more endogenous serotonin in the synaptic cleft for a longer period, increasing the chance of it binding to the post-synaptic receptors.

Questions & Discussion

  • Question (Internal Reflection/Student Prep): Is the difference between 70mV-70\,mV and 55mV-55\,mV always the same for every neuron?

  • Response: The lecture implies these are standard thresholds used in the textbook as generalized estimates for most neurons during rest and activation.

  • Discussion on Evolution: The lecturer notes that humans may have higher levels of norepinephrine than currently needed because the body's "hardware" is still evolved for survival in primordial environments, leading to modern anxiety.

  • Closing Remark: Students are encouraged to review the supplemental videos (Animation on Thought and Two-Minute Neurology series) in the provided order for better synthesis.