5-1-Genes-To-Behavior
Chapter 10: Pathways between Genes and Behavior
From Genes to Behavior
External Cues:
Environmental triggers that influence behavior.
Internal States:
Conditions affecting behavioral responses, such as hunger.
Neural Networks:
Connections among neurons responsible for processing information.
Central Decision Making Process:
Example: how sleepiness may modulate responses to cues.
Epigenetic Control of Gene Expression:
The regulatory processes that influence how genes are expressed based on environmental stimuli.
Functional Genomics
Levels of Analysis:
Behavioral Level: Observation of individual behaviors.
Molecular Level: Study of gene expression and molecular functions.
Cellular Level: Examination of neuronal activity and cell function.
Systems Level: Interaction of neural circuits that comprise the brain.
Individual Behavior: Interaction of genetic and environmental factors affecting a single organism.
Social Behavior: Understanding of group dynamics and social networks, linking behavior to evolutionary and societal contexts.
Behavior Modifying Drugs
Action of Drugs:
Certain drugs can mimic neurotransmitters, either enhancing or inhibiting pathways in the brain.
Selected Recreational Drugs:
Cocaine, Morphine, and Heroin: Act primarily on endorphin pathways in the hypothalamus.
Mescaline and Nicotine: Mimic specific neurotransmitter actions.
Amphetamines: Influence dopamine and norepinephrine pathways affecting the reward system and arousal.
Brain Chemical Equivalents:
Endorphins: Associated with pain relief and stress management.
Dopamine: Responsible for motivation and reward pathways.
Norepinephrine: Mediates the fight or flight response.
Neuronal Communication
Post-Synaptic Action:
A receiving neuron determines whether to excite the next neuron based on the signal received.
Brain Cells:
Neurons: Responsible for transmitting signals.
Glial Cells: Support cells constituting 50% of brain mass; their quantity correlates with overall brain size.
Behavioral Genetics Overview
Mechanisms of Action:
Example: MAOA enzyme's role in neurotransmitter degradation influencing dendrites, vesicle encapsulation, breakdown, release, and receptor activity.
Cell Signaling
Three Stages of Cell Signaling:
Ligand-Gated Channel Receptors: Activate in response to specific ligands/ions.
Tyrosine Kinase Receptors: Involved in signaling pathways leading to transcription changes.
G-Protein Coupled Receptors: Involved in a variety of signaling responses by changing conformation and interacting with proteins.
Nerve Impulse
Definition:
An electrical current leading to signal transmission.
Action Potential Process:
Voltage-gated channels open/close in response to electric changes:
Net positive charge outside and net negative charge inside during depolarization.
Potential restoration occurs after signal transmission.
Chemical Synapses
Depolarization: Initiates neurotransmitter release.
Hyperpolarization: Inhibitory signal processing.
Neurotransmitter Activity: Interactions with post-synaptic receptors, leading to excitatory or inhibitory responses.
Gene-Environment Interactions
Discussion on MAOA and the 5-HTTLPR polymorphisms affects phenotypes and neurotransmitter systems in monoaminergic synapses.
Vesicular Monoamine Transporter (VMAT)
Components of the synapse include:
Pre and postsynaptic players, biosynthesis enzymes, monoamine receptors, and metabolizing enzymes such as monoamine oxidase (MAO).
Monoamine Oxidase A (MAOA)
Function:
Degrades amine neurotransmitters, including dopamine, norepinephrine, and serotonin.
Localized to the outer mitochondrial membrane with multiple isoforms identified.
Adjacent to MAOB in genetic mapping.
Effects of Psychostimulants
Certain drugs, including:
Methylphenidate (Ritalin®)/Cocaine: Increases DA at synapses via blocking DAT (reuptake).
Amphetamines/Meth: Alter DA levels by enhancing or diminishing proper signaling; block VMAT and decrease synaptic DA, reverse DAT to release into synapse.
Antidepressants and Serotonergic Pathway
Antidepressant Mechanisms:
Modulation of serotonergic synapses, increasing serotonin uptake, receptor activation, and blocking MAO activity.
5-HTTLPR Gene
Function:
Encodes the serotonin re-uptake transporter responsible for serotonin availability.
Chromosomal Location:
Located on Chromosome 17 and features two prominent alleles: S and L alleles affecting brain function significantly.
Circuit Dynamics
Excitatory and Inhibitory Interactions:
Feedforward Excitation: Initiated by sensory cues, stimulating neurotransmitter release.
Feedforward Inhibition: Modulates the reactive pathways by neurotransmitter binding.
Micro Networks
A neuron can engage with up to 10,000 presynaptic neurons, and each neuron can connect with up to 10,000 postsynaptic neurons, allowing complex combinatorial neuronal circuit arrangements.
Key Takeaways
Remember:
Levels of study in behavioral genetics.
Drug mechanisms mimicking neurotransmitter actions.
Understanding of action potentials and synaptic structures.
Impact of MAO-A variants and serotonin transporter gene variations on synaptic function.