Origins of Behavioral Neuroscience — Chapter 1

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Vocabulary flashcards covering key terms from the Origins of Behavioral Neuroscience chapter.

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29 Terms

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mind-brain problem

The question of how the mind relates to the brain and whether mental events are separate from, identical to, or produced by brain activity.

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monism

The belief that mind and body are the same substance; in neuroscience, the mind is produced by physical brain (materialistic monism) or that both are aspects of one substance.

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dualism

The belief that mind and body are separate; the mind may influence the brain, and is often considered nonphysical.

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Descartes’ hydraulic model

René Descartes’ idea that nerves are hollow tubes carrying animal spirits; movement is produced when these fluids flow, directed by the pineal gland.

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animal spirits

The hypothetical fluid Descartes proposed to flow through nerves to produce movement and sensation.

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pineal gland - Descartes theory

A small brain structure Descartes believed directed the flow of animal spirits; he called it the seat of the soul.

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localization

The principle that specific areas of the brain are responsible for specific functions.

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equipotentiality

The idea that brain functions are distributed and not confined to a single, localized area.

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Broca’s area

A region in the left frontal lobe associated with speech production; damage can cause expressive aphasia.

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phrenology

A 19th-century theory that skull bumps reflect underlying brain areas controlling faculties; associated with 35 claimed ‘faculties.’

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Fritsch & Hitzig

Pioneering 1870 experiments showing electrical stimulation of dog cortex could evoke movement, supporting localization of function.

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Helmholtz

Physiologist who measured nerve conduction speed and showed it is slower than electrical signals in wires, supporting a mechanistic view of the nervous system.

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Decade of the Brain

A designation in the 1990s to raise public awareness of brain research and expand neuroscience.

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DNA

Deoxyribonucleic acid; the double-helix molecule that stores genetic information using bases A, T, G, C.

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gene

The biological unit that directs cellular processes and transmits inherited characteristics; located on chromosomes (and some in mitochondria).

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chromosome

DNA-containing structures in the cell nucleus; humans have 46 chromosomes (23 pairs); sex chromosomes are X and Y.

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allele

Alternative forms of a gene; different versions can be dominant or recessive and produce different phenotypes.

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X-linked

Traits caused by genes on the X chromosome, often more apparent in males due to having a single X chromosome.

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polygenic

Traits influenced by many genes, such as height, intelligence, and many behavioral characteristics.

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Huntington’s disease

A single-gene, autosomal-dominant disorder used to illustrate a genetic basis for disease and behavior.

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Human Genome Project

International effort to map and sequence all human genes; revealed about 21,000 protein-coding genes and extensive noncoding DNA.

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ENCODE project

Research initiative to identify functional elements in the noncoding genome and understand gene regulation.

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junk DNA

Noncoding DNA; much of it is functional and regulates gene expression; noncoding regions influence development and evolution.

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HACNS1

A human-specific regulatory DNA element that, when inserted into a mouse embryo, can turn on genes involved in the forearm/thumb development.

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CRISPR

Clustered regularly interspaced short palindromic repeats; a gene-editing technology using Cas enzymes to cut and replace DNA sequences.

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gene expression

The process by which information from a gene is used to synthesize functional products (mainly proteins), affecting development and brain function.

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heritability

The proportion of variation in a trait in a population that is due to genetic factors; estimated via twin studies and influenced by environment and population studied.

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identical vs fraternal twins

Identical twins share all genes (monozygotic); fraternal twins share about 50% of genes (dizygotic); used to estimate heritability.

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vulnerability

The concept that genes provide a predisposition for a disorder, which may require environmental triggers to manifest; gene-environment interaction.