NERVOUS SYSTEM. Chapter 48-49

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NERVOUS SYSTEM Chapter 48-49

Nervous System Function: coordinates and controls bodily functions with nerves and electrical impulses The system is composed of different types of nerve cells called neurons One neuron may communicate with thousands of other neurons Communication between neurons can be long-distance electrical signals or short-distance chemical signals

Nervous System In all vertebrates, the nervous system shows a high degree of cephalization and distinct CNS and PNS components Central nervous system (CNS) The brain provides the integrative power that underlies the complex behavior of vertebrates The spinal cord integrates simple responses to certain kinds of stimuli and conveys information to and from the brain Brain Spinal cord Peripheral nervous system (PNS) Cranial nerves Ganglia outside CNS Spinal nerves Figure 48.19

Information Processing The nervous system processes information through detection, generation, transmission, and integration of signal information Essentially: Sensory input, integration, and motor output Sensory input Sensor Integration Motor output Figure 48.3 Effector Peripheral nervous system (PNS) Central nervous system (CNS)

Divisions of the Nervous System 2 main divisions are the Central and Peripheral Nervous systems CNS and PNS The CNS integrates and processes information from the body The PNS transmits information to and from the CNS

Peripheral Nervous System Divisions of PNS: Sensory and Motor division Sensory = sends signals to the CNS from receptors Motor = send signals away from the CNS to the parts of the body Motor division can be separated into the Somatic nervous system and the Autonomic nervous system SNS and ANS Autonomic nervous system divides into Parasympathetic and Sympathetic divisions

Peripheral Nervous System Somatic nervous system Carries signals to skeletal muscles and is voluntarily controlled Autonomic nervous system Involuntarily regulates the internal environment Carries signals to cardiac muscle, smooth muscle, and glands

Peripheral Nervous System The ANS division have antagonistic effects on target organs Sympathetic division: fight-or-flight response Parasympathetic division: promotes a return to selfmaintenance functions and resting and digesting

Parasympathetic division Sympathetic division Action on target organs: Action on target organs: Location of preganglionic neurons: brainstem and sacral segments of spinal cord Constricts pupil of eye Stimulates salivary gland secretion Dilates pupil of eye Inhibits salivary gland secretion Location of preganglionic neurons: thoracic and lumbar segments of spinal cord Neurotransmitter released by preganglionic neurons: acetylcholine Constricts bronchi in lungs Slows heart Cervical Sympathetic ganglia Relaxes bronchi in lungs Accelerates heart Neurotransmitter released by preganglionic neurons: acetylcholine Location of postganglionic neurons: in ganglia close to or within target organs Stimulates activity of stomach and intestines Stimulates activity of pancreas Thoracic Inhibits activity of stomach and intestines Inhibits activity of pancreas Stimulates glucose release from liver; inhibits gallbladder Location of postganglionic neurons: some in ganglia close to target organs; others in a chain of ganglia near spinal cord Neurotransmitter released by postganglionic neurons: acetylcholine Stimulates gallbladder Promotes emptying of bladder Lumbar Stimulates adrenal medulla Inhibits emptying of bladder Neurotransmitter released by postganglionic neurons: norepinephrine Figure 49.8 Promotes erection of genitalia Synapse Sacral Promotes ejaculation and vaginal contractions

Types of Neurons Neurons have a wide variety of shapes that reflect their input and output interactions Dendrites Axon Cell body Figure 48.5 (a) Sensory neuron (b) Interneurons (c) Motor neuron

Types of Neurons Sensory neurons transmit information from sensory receptors to the CNS Detects external stimuli and internal conditions Interneurons integrate the information in the CNS This can be in the spinal cord or connect up to the brain Motor neurons transmit information away from the CNS Neurons communicate with effector cells/organs (muscles and glands)

Stages of Information Processing Reflex arc body s automatic response to a stimulus This pathway includes: Receptor Sensory neuron Interneuron Motor neuron Effector organ

Reflex Arc This is a much faster response compared to the typical stimulus-response transmission pathways The reason is that reflex arcs do not involve the integration of the brain and have fewer neuron connections compared to other pathways Reflex arcs also do not require conscious control and involuntarily occur which leads to some of our innate responses

Reflex Arc 2 Sensors detect 3 Sensory neurons a sudden stretch in the quadriceps. convey the information to the spinal cord. Quadriceps muscle Cell body of sensory neuron in dorsal root ganglion 4 The sensory neurons communicate with motor neurons that supply the quadriceps. The motor neurons convey signals to the quadriceps, causing it to contract and jerking the lower leg forward. White matter Gray matter 5 Sensory neurons from the quadriceps also communicate with interneurons in the spinal cord. 1 The reflex is initiated by tapping the tendon connected to the quadriceps (extensor) muscle. Hamstring muscle Spinal cord (cross section) Sensory neuron Motor neuron Interneuron 6 The interneurons inhibit motor neurons that supply the hamstring (flexor) muscle. This inhibition prevents the hamstring from contracting, which would resist the action of the quadriceps. Figure 49.3

Neuron Structure Dendrites Cell body Axon hillock Nucleus Axon Signal direction Synapse Presynaptic cell Myelin sheath Postsynaptic cell Figure 48.4 Synaptic terminals

Neuron Structure Cell body = contains the organelles Dendrites = highly branched extensions that receive signals from other neurons Axon = cytoplasmic extension that transmits signals to other cells at synapses May be covered with Schwann cells which is a fatty cell wrapped around the axon to form the myelin sheath

Neuron Structure Nodes of Ranvier = space between the Schwann cells on the axon Axon terminals = contains the vesicles of neurotransmitters (chemical messengers that act as ligands)

Supporting Cells (Glia) Essential for the structural integrity of the nervous system and for the normal functioning of neurons CNS Astrocytes supplies nutrients to neurons in the CNS Oligodendrocytes protection Ependymal cells lines ventricles and has cilia to move cerebrospinal fluid Microglial cells protection against microorganisms and clean up cellular debris PNS Schwann cells protection

Axon Myelin sheath Schwann cell Nodes of Ranvier Node of Ranvier Layers of myelin Schwann cell Nucleus of Schwann cell Axon 0.1 µm

Nerve Physiology 4 Steps: - Resting membrane potential - Depolarization after threshold - Action Potential - Repolarization

Nerve Physiology Membranes of neurons are polarized due to an electrical potential difference called the resting membrane potential The inside of the cell is negative relative to the outside and is measured using a voltmeter The resting membrane potential is when a neuron is not transmitting a signal Resting membrane potential = - 70mV

Resting Membrane Potential In all neurons, the resting membrane potential depends on the ionic gradients that exist across the plasma membrane Ion pumps and ion channels maintain the resting potential of a neuron CYTOSOL [Na + ] 15 mm [K + ] 150 mm [Cl ] 10 mm [A ] 100 mm EXTRACELLULAR FLUID + [Na + ] 150 mm + + + + [K + ] 5 mm [Cl ] 120 mm Figure 48.6 Plasma membrane

Resting Membrane Potential The concentration of Na + is higher in the extracellular fluid than in the cytosol while the opposite is true for K + A neuron that is not transmitting signals contains many open K + channels and very few open Na + channels in its plasma membrane The diffusion of K + and Na + through these channels leads to a separation of charges across the membrane, producing the resting potential

Why is the charge -70 mv? Inner chamber Outer 90 mv chamber Inner +62 mv chamber Outer chamber 150 mm KCL + 5 mm KCL 15 mm NaCl + 150 mm NaCl + Cl + Potassium channel + K + Artificial membrane Cl Na + Sodium channel + Figure 48.7 (a) Membrane selectively permeable to K + (b) Membrane selectively permeable to Na +

Why is the charge -70 mv? K + is moved into the cell and Na + is moved outside due to the action of the Na/K pump If K + is allowed to flow back to equilibrium, the membrane would be at -90mV Separately, if Na + is allowed to flow to equilibrium, the membrane would be at +62 mv

Why is the charge -70 mv? Because there are more K + channels open compared to Na + channels AND there are negative proteins inside the cell, the charge difference settles to -70mV Basically, a few positive things are leaking back into the cell which cancels out some of the -90mV difference from the K+ flow

Action Potential Steps Gated ion channels open or close in response to the binding of a specific ligand or a voltage change The response is a change in the membrane potential When ion channels are stimulated, two different responses can occur: hyperpolarization or depolarization Both are called graded potentials because the magnitude of the change in membrane potential varies with the strength of the stimulus

Membrane potential (mv) Cell Responses Some stimuli trigger a hyperpolarization An increase in the magnitude of the membrane potential (larger negative difference from outside to inside) +50 0 50 Threshold Stimuli Resting potential Hyperpolarizations Figure 48.9 100 0 1 2 3 4 5 Time (msec) (a) Graded hyperpolarizations produced by two stimuli that increase membrane permeability to K +. The larger stimulus produces a larger hyperpolarization.

Membrane potential (mv) Cell Responses Other stimuli trigger a depolarization A reduction in the magnitude of the membrane potential (move towards a positive difference from outside to inside) Figure 48.9 +50 0 50 Threshold Stimuli Resting potential Depolarizations 100 0 1 2 3 4 5 Time (msec) (b) Graded depolarizations produced by two stimuli that increase membrane permeability to Na+. The larger stimulus produces a larger depolarization.

Membrane potential (mv) Cell Responses A stimulus strong enough to produce a depolarization that reaches the threshold will trigger an action potential Threshold = membrane voltage amount needed to cause an action potential - 55 mv Figure 48.9 +50 0 50 Stronger depolarizing stimulus Action potential Threshold Resting potential 100 0 1 2 3 4 5 6 Time (msec) (c) Action potential triggered by a depolarization that reaches the threshold.

Action Potential Steps An action potential is a brief all-or-none depolarization of a neuron s plasma membrane that carries information along axons Both voltage-gated Na + channels and voltage-gated K + channels are involved in the production of an action potential Voltage-gated channels rely of electrical signals rather than ligands

Action Potential Steps Depolarization Membrane Na + channels open which allows Na + to diffuse into the cell This causes the charge on the neuron membrane to change to positive inside and negative outside Action Potential Propagation of the signal is continued depolarization down the axon

Action Potential Steps Repolarization As the action potential subsides K + channels open, and K + flows out of the cell which changes the charge again on the membrane Na/K pump restores the ion concentration differences with the use of ATP This comes back to the resting membrane potential A refractory period follows the action potential during which a second action potential cannot be initiated

Conduction of Action Potentials An action potential can travel long distances by regenerating itself along the axon The opening of Na+ channels triggers the opening of even more channels The speed of an action potential increases with the diameter of an axon

Conduction of Action Potentials Action potentials in myelinated axons jump between the nodes of Ranvier in a process called saltatory conduction This allows the signal to travel faster down the axon Schwann cell Depolarized region (node of Ranvier) Myelin sheath Cell body Figure 48.13 + + + + + + + + + Axon

Synapse In an electrical synapse, electrical current flows directly from one cell to another via a gap junction The vast majority of synapses are chemical synapses In a chemical synapse, a presynaptic neuron releases chemical neurotransmitters, which are stored in the synaptic terminal The neurotransmitters will travel through the space between the cells called the synaptic cleft to bind to the post-synaptic neuron

5 µm Synapse Postsynaptic neuron Synaptic terminal of presynaptic neurons Figure 48.14

Synapse When an action potential reaches the terminal a voltage-gated Ca 2+ channel opens to allow Ca 2+ to flow into the axon terminal Ca 2+ acts a second messenger and causes the vesicles holding the neurotransmitters to fuse with the plasma membrane The final result is the release of neurotransmitters into the synaptic cleft

Synapse Presynaptic cell Postsynaptic cell Synaptic vesicles containing neurotransmitter Presynaptic membrane 5 Na + K + Neurotransmitter Postsynaptic membrane Voltage-gated Ca 2+ channel Ligandgated ion channel 1 Ca 2+ 2 4 Postsynaptic membrane 6 Synaptic cleft 3 Figure 48.15 Ligand-gated ion channels

Direct Synaptic Transmission The process of direct synaptic transmission involves the binding of neurotransmitters to ligand-gated ion channels Neurotransmitter binding causes the ion channels to open, generating a postsynaptic potential Postsynaptic potentials fall into two categories: Excitatory (stimulatory) or Inhibitory

Direct Synaptic Transmission After its release, the neurotransmitter diffuses out of the synaptic cleft May be taken up by the pre-synaptic cell or degraded by enzymes

Neurotransmitters Chemical messengers that act on cells to create a response The same neurotransmitter can produce different effects in different types of cells Types: Acetylcholine, biogenic amines, various amino acids and peptides, and certain gases

Neurotransmitters Acetylcholine is one of the most common neurotransmitters in both vertebrates and invertebrates Can be inhibitory or excitatory Used in muscle contraction Biogenic amines: include epinephrine, norepinephrine, dopamine, and serotonin Are active in the CNS and PNS

Neurotransmitters Various amino acids and peptides are active in the brain Gases such as nitric oxide and carbon monoxide are local regulators in the PNS

Structure of the Brain Cerebrum, cerebellum, brainstem, and diencephalon

Anatomy Gray matter no myelin sheath Located on outside in brain and inside in spinal cord White matter has myelin sheath Located on outside in spinal cord and inside in brain Gray matter White matter Ventricles Figure 49.5

Brainstem The brainstem consists of three parts: medulla oblongata, pons, and midbrain The medulla oblongata contains centers that control heart rate, blood pressure, breathing, swallowing, and vomiting The pons controls breathing The midbrain contains centers for passing ascending and descending signals

Arousal and Sleep A diffuse network of neurons called the reticular formation is present in the core of the brainstem A part of the reticular formation, the reticular activating system (RAS) regulates sleep and arousal Eye Reticular formation Input from touch, pain, and temperature receptors Input from ears Figure 49.10

Cerebellum The cerebellum is important for coordination and balance Also involved in learning and remembering motor skills

Diencephalon The embryonic diencephalon develops into three adult brain regions: epithalamus, thalamus, and hypothalamus The epithalamus includes the pineal gland (releases melatonin) and the choroid plexus (capillaries that produce cerebrospinal fluid) The thalamus sends sensory and motor information to the cerebrum

Diencephalon The hypothalamus regulates homeostasis Basic survival behaviors such as feeding, fighting, fleeing, and reproducing Part of the limbic center

Cerebrum The cerebrum contains right and left cerebral hemispheres Each consist of cerebral cortex overlying white matter and basal nuclei (regions of gray matter inside brain) centers for planning and learning movement sequences Left cerebral hemisphere Corpus callosum Right cerebral hemisphere Basal nuclei Figure 49.13

Cerebrum A thick band of axons, the corpus callosum provides communication between the right and left cerebral cortices In humans, the largest and most complex part of the brain is the cerebral cortex, where sensory information is analyzed, motor commands are issued, and language is generated

Cerebrum Each side of the cerebral cortex has four lobes Frontal, parietal, temporal, and occipital Frontal lobe Parietal lobe Frontal association area Speech Smell Hearing Auditory association area Speech Taste Somatosensory association area Reading Visual association area Vision Figure 48.27 Temporal lobe Occipital lobe

Cerebrum In the somatosensory cortex and motor cortex neurons are distributed according to the part of the body that generates sensory input or receives motor input Frontal lobe Parietal lobe Toes Genitalia Lips Jaw Tongue Figure 48.28 Primary motor cortex Tongue Pharynx Abdominal organs Primary somatosensory cortex

Emotions The limbic system is a ring of structures around the brainstem Thalamus Hypothalamus Prefrontal cortex Figure 48.30 Olfactory bulb Amygdala Hippocampus

Emotions This limbic system includes three parts of the cerebral cortex: amygdala, hippocampus, and olfactory bulb These structures attach emotional feelings to survival-related functions Structures of the limbic system form in early development and provide a foundation for emotional memory, associating emotions with particular events or experiences

Memory and Learning The frontal lobes are a site of short-term memory Interact with the hippocampus and amygdala to consolidate long-term memory Many sensory and motor association areas of the cerebral cortex are involved in storing and retrieving words and images

Neural Stem Cells The adult human brain contains stem cells that can differentiate into mature neurons The induction of stem cell differentiation and the transplantation of cultured stem cells are potential methods for replacing neurons lost to trauma or disease Figure 49.24