Biological Psychology Kalat 12th Edition Solutions Manual
Biological Psychology Kalat 12th Edition Solutions Manual
Biological Psychology Kalat 12th Edition Solutions Manual
Manual
full chapter at: https://testbankbell.com/product/biological-
psychology-kalat-12th-edition-solutions-manual/
CHAPTER 1
NERVE CELLS AND NERVE IMPULSES
Chapter Outline
I. The Cells of the Nervous System
A. Neurons and Glia
1. The nervous system is composed of two types of cells: neurons and glia.
a. Neurons: Receive information and transmit it to other cells.
b. Glia: Serve many functions that are difficult to summarize.
c. The human brain contains approximately 100 billion neurons (though that
estimate varies from person to person).
2. Santiago Ramón y Cajal (1852-1934), a Pioneer of Neuroscience
a. Used staining techniques to reveal that small gaps separate the tips of one
neuron from another. This discovery showed that the brain—like the rest of the
body—is composed of individual cells.
3. The Structure of an Animal Cell
a. Neurons contain the same basic structures of other animal cells.
b. Membrane (plasma membrane): Composed of two layers of fat molecules,
this membrane allows some small uncharged chemicals to flow both into and
out of the cell. Protein channels allow a few charged ions to cross the
membrane, but most chemicals are unable to cross.
c. Nucleus: The structure that contains the chromosomes.
d. Mitochondrion: The structure that provides the cell with energy. It requires
fuel and oxygen to function.
e. Ribosomes: Site of protein synthesis in the cell.
f. Endoplasmic reticulum: A network of thin tubes that transports newly
synthesized proteins to other locations. Ribosomes may be attached.
4. The Structure of a Neuron
a. The most distinctive structural feature of neurons is their shape, which varies
enormously.
b. Larger neurons contain four major components: dendrites, cell body, axon, and
presynaptic terminal. The tiniest neurons may lack axons and well-defined
dendrites. Compare the structure of these components in the following two
types of neurons:
i. A motor neuron: Conducts impulses to muscles and glands from the
spinal cord.
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ii. A sensory neuron (receptor neurons): Sensitive to certain kinds of
stimulation (e.g., light, touch, etc.).
c. Neuron components:
i. Dendrites: Branching fibers that extend from the cell body and get
narrower at their end. The dendrite’s surface is lined with specialized
synaptic receptors, at which the dendrite receives information from
other neurons.
ii. Dendritic spines: Short outgrowths found on some dendritic branches.
iii. Cell body (soma): Contains the nucleus, ribosomes, mitochondria, and
other structures found in most cells.
iv. Axon: A long, thin fiber (usually longer than dendrites), which is the
information-sending part of the neuron, sending an electrical impulse
toward other neurons, glands, or muscles.
v. Myelin sheath: Insulating covering found on some vertebrate axons.
vi. Nodes of Ranvier: Interruptions along the myelin sheath.
vii. Presynaptic terminal (end bulb): Swelling at the tip of the axon. The
part of the neuron that releases chemicals that cross the junction between
one neuron and the next.
d. Neurons may have any number of dendrites, but are limited to no more than
one axon (which may have branches).
e. Other terms associated with neurons:
1) Afferent axons: Brings information into a structure.
2) Efferent axons: Sends information away from a structure.
3) Interneurons (intrinsic neurons): Entirely located within a single
structure of the nervous system.
4. Variations among Neurons
a. Neurons vary enormously in size, shape, and function.
b. A neuron’s function is closely related to its shape.
c. A neuron’s shape is plastic (changeable) as new experiences can modify the
shape of a neuron.
5. Glia
a. Glia (neuroglia) are the other major component of the nervous system. Glia
have many different functions but they do not transmit information like
neurons.
b. Glia are smaller and more numerous than neurons. Several types of glia exists
to perform different functions.
c. Astrocytes: A type of glia that absorbs chemicals released by axons and later
returns those chemicals back to the axon to help synchronize the activity of
neurons. Astrocytes remove waste products as well, particularly those created
after neurons die. Astrocytes also cause blood vessels to dilate to bring in more
nutrients at times of increased brain activity. They act as a recycling system for
glutamate released by neurons (absorbing excess glutamate then converting it
to glutamine and passing it back into the neurons).
d. Microglia: Very small cells that remove waste material as well as viruses,
fungi, and other microorganisms.
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2. In the absence of any outside disturbance (i.e., at rest), the membrane maintains an
electrical polarization (i.e., a difference in electrical charge between two locations)
that is slightly more negative on the inside relative to the outside. This difference in
electrical potential or voltage is known as the resting potential.
3. The resting potential is measured by very thin microelectrodes. A typical resting
membrane potential is -70 millivolts (mV). This may vary from one neuron to
another.
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c. Relative refractory period: Sodium gates are capable of opening, but
potassium channels remain open; a stronger than normal stimulus (i.e.,
exceeding threshold) will initiate an action potential.
d. In most neurons, the absolute refractory period is about 1 ms and the relative
refractory period is another 2-4 ms.
C. Propagation of the Action Potential
1. The action potential begins at the axon hillock (a swelling located where the axon
exits the cell body).
2. The action potential is regenerated due to sodium ions moving down the axon,
depolarizing adjacent areas of the membrane.
3. Propagation of the action potential: Transmission (movement) of an action
potential down an axon. The action potential moves down the axon by regenerating
itself at successive points on the axon.
4. The refractory periods prevent the action potentials from moving in the opposite
direction (i.e., toward the axon hillock).
D. The Myelin Sheath and Saltatory Conduction
1. Myelin: An insulating material composed of fats and proteins found on some
vertebrate axons. Myelin greatly increases the speed of propagation.
2. Myelinated axons: Axons covered with a myelin sheath, found only in vertebrates.
3. Nodes of Ranvier: Short, unmyelinated sections on a myelinated axon.
4. Saltatory conduction: The “jumping” of the action potential from node to node.
5. Some diseases, including multiple sclerosis, destroy the myelin along axons; loss of
the myelin sheath slows down or prevents the propagation of action potentials.
E. Local Neurons
1. Small neurons with short dendrites and a short (if any) axon. Local neurons do not
follow the all-or-none law.
2. Graded potentials: Membrane potentials that vary in magnitude in proportion to
the intensity of the stimulus. Graded potentials get smaller as they travel.
Learning Objectives
1. Describe neurons and glia, the cells that constitute the nervous system.
2. Summarize how the blood–brain barrier relates to protection and nutrition of neurons.
3. Explain how the sodium–potassium pump and the properties of the membrane lead to the
resting potential of a neuron.
4. Discuss how the movement of sodium and potassium ions produces the action potential and
recovery after it.
5. State the all-or-none law of the action potential.
Key Terms
2. Demonstrating the Action Potential: With the use of dominos, explain how the action
potential works. Dominos and a stick or thin wooden ruler are required. Arrange dominos in
a straight line and tell your students that this represents a neuron. After pushing the first
domino, all others fall in sequence: this provides an example of how an action potential
begins in one area of a neuron (axon hillock) and travels down the axon. The concept of the
refractory period is demonstrated when you cannot knock over the dominos again until you
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reset them. Also, by giving the first domino a slight touch (which is not strong enough to
knock it over) you can allow students to conceptualize the all-or-none principle (an action
potential will not occur unless the stimulus which creates it forces the neuron to reach its
threshold.)
Source: Wagor, W. F. (1990) Using dominos to help explain the action potential. In V.
P. Makosky, C. C. Sileo, L. G. Whittemore, C. P. Landry, & M. L. Skutley (Eds.)
Activities handbook for the teaching of psychology: Vol. 3. (pp. 72-73). Washington
D.C.: American Psychological Association.
For smaller classes, an additional exercise for the action potential can also be found here:
Reardon, R., Durso, R. T., and Wilson, D. A. (1994). Neural coding and synaptic
transmission: participation exercises for introductory psychology. Teaching of
Psychology, 21, 96-99.
3. The Colossal Neuron: Acting out physiological psychology. This is an interesting class
demonstration that works well even in large lecture classes. The demonstration involves 30
students joining to construct a “functional” colossal neuron. Principles such as the
movement of ions during the action potential and synaptic transmission are demonstrated.
The full instructions for this exercise can be found in the article below:
Hamilton, S. B., Knox, T. A. (1985). The colossal neuron: acting out physiological
psychology. Teaching of Psychology, 12, 153-156.
4. Action Potential–Epilepsy: In this activity, students simulate how an action potential starts
in a neuron using dried peas and beans to represent ions. The activity provides student with a
better understanding of how Na+ and K+ ions move across the membrane and the
mechanisms that allow a neuron to remain at rest. It also allows students to apply knowledge
of how the action potential works under normal conditions to what may be occurring during
epilepsy.
The exercise was developed by Thomas Conley and Beth Shepley for the Neuroscience
Laboratory and Classroom Activities Manual. The full instructions can be found at:
http://www.nabt.org/sites/S1/index.php?p=85
5. Neuron slide show: To demonstrate the many unique shapes of neurons in the nervous
system, supplement the images from the text with images downloaded from the following
Web site:
http://faculty.washington.edu/chudler/gall1.html
After students have viewed the slides, have them discuss the following two questions about
neurons.
6. To illustrate the difference between propagation of the action potential along unmyelinated
and myelinated axons, use the graphic found on
http://www.brainviews.com/abFiles/AniSalt.htm. The class can discuss other factors that
affect the speed of propagation along a neuron, such as the diameter of the neuron and why
some neurons are myelinated and some are unmyelinated.
7. To demonstrate the anatomy of a neuron, take an arm-length latex glove and blow it up (or
simply use your forearm.) The fingers represent the multiple dendrites that convey
information to the cell body (the hand). Information is consolidated at the cell body and an
action potential will be initiated at the axon hillock (the wrist). The arm is the axon, which
carries the action potential away from the cell body.
Suggested Other Multimedia Resources
1. “Nerve Impulse Conduction” (Insight Media, 29 min): Explores the electrochemical nature
of nerve impulses and discusses how certain drugs and chemicals interfere with this process.
2. “The Behaving Brain” (The Annenberg/CPB Collection, 30 min): Engages students in how
the brain works; includes a simple and easy overview of neuron structure and function. Part
of the Discovering Psychology series at http://www.learner.org/resources/series138.html.
3. “The Graphic Brain” (Timothy J. Teyler; Brooks/Cole): Provides modules covering many
neurophysiological phenomena, such as the movement of ions across an axon membrane,
the movement of the action potential along an axon, second-messenger activation, and
lateral inhibition as well as other computer-animated presentations.
4. “Neurons in Action: Computer Simulations with Neurolab” (John W. Moore and Ann E.
Stuart; Sinauer Associates): Allows students to perform virtual electrophysiology
experiments on neurons; enhances students’ understanding of the nerve impulses.
5. Many additional resources and tools are available on Cengage’s MindTap for this text.
http://faculty.washington.edu/chudler/introb.html#bb
This site was designed by Dr. Eric Chudler at the University of Washington and is one of the
best resources for teaching basic biological psychology on the Web. Although developed for
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secondary students, it provides a great overview for both the neuronal structure and
neurophysiology discussed in this chapter.
http://nerve.bsd.uchicago.edu/med98a.htm
This electronic textbook, The Nerve Impulse, is written by F. Bezanilla, and gives a
thorough overview of the molecular basis of the action potential and other membrane
properties.
http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/E/ExcitableCells
This online biology textbook is written by J. W. Kimball. The section on excitable cells
gives a concise overview of the signaling properties of neurons.
Cocaine
Along with its ability to induce euphoria, cocaine-like Novocaine is a local anesthetic.
Discuss the effect that systemically administered cocaine could have on the functioning of
the nervous system.
Glia
Given that glia have been shown to have more and more functions in the nervous system,
the original name of “glue” seems more and more inappropriate. What would be a better
description for glia, given what we now know about them?
Resting Potential
Neurons, by some estimates, spend up to 40% of their energy maintaining a resting
membrane potential of about -70 mV. Why is this a worthwhile investment? What would be
the impact on our behavior if the resting membrane potential was shifted either more
negative, to about -90 mV, or more positive, to about -65 mV? (Assume that everything else
about the neuron, including the threshold, remains unchanged.)
Blood-Brain Barrier
The blood-brain barrier protects the brain from infectious agents in the blood and also
regulates which ions or other charged molecules can enter the brain from the blood supply.
Despite these protective functions, the barrier does not exist in all parts of the brain. Why
might this be the case?
Answer: The structure of heroin and morphine obviously differ in regards to how they affect
the brain. Given that the blood-brain barrier is a web of tightly packed cells blocking
substances from entering the brain, it can be inferred that the structure of heroin is smaller,
or in some way more capable of being diffused through the blood-brain barrier.
Module 1.2
1. Suppose the threshold of a neuron were the same as the neuron’s resting potential. What
would happen? At what frequency would the cell produce action potentials?
Answer: The resting potential of a neuron is typically around -70 millivolts (mV). If the
threshold of a neuron is also -70 mV, or the same as the neuron’s resting potential, an action
potential will occur, and the membrane will open its sodium channels and permit sodium ions
to flow into the cell. The membrane will return to its resting potential, but the inside of the
neuron now has slightly more sodium ions and slightly fewer potassium ions than before.
Eventually, the sodium–potassium pump restores the original distribution of ions, but that
diffusion process takes time.
If the threshold is equal to the resting potential, the pump will not be able to keep up with this
action, and sodium will accumulate within the axon. Excessive buildup of sodium will be
toxic to the cell, and likely, lead to its death.
2. In the laboratory, researchers can apply an electrical stimulus at any point along the axon,
making action potentials travel in both directions from the point of stimulation. An action
potential moving in the usual direction, away from the axon hillock, is said to be traveling in the
orthodromic direction. An action potential traveling toward the axon hillock is traveling in the
antidromic direction. If we started an orthodromic action potential at the axon hillock and an
antidromic action potential at the opposite end of the axon, what would happen when they met at
the center? Why?
Answer: When the two impulses met in the center, both would stop, because the point at
which they met would be surrounded on both sides by axon areas in their refractory periods.
Here is one way to use antidromic impulses in research: Suppose you are interested in an
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axon that terminates in one part of the brain, and you want to know where the axon
originated. You could electrically stimulate that axon, then record from various places and
try to trace the antidromic impulse back to the origin of the axon. Of course, this will be
ineffective if the cell has a high spontaneous firing rate, because orthodromic impulses will
cancel the antidromic impulses at their point of collision.
3. If a drug partly blocks a membrane’s potassium channels, how does it affect the action
potential?
Answer: Potassium ions exit the cell more slowly than usual after an action potential.
Therefore, the action potential will be prolonged.