Neural Integration II: The Autonomic Nervous System and Higher-Order Functions
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1 16 Neural Integration II: The Autonomic Nervous System and Higher-Order Functions PowerPoint Lecture Presentations prepared by Jason LaPres Lone Star College North Harris
2 An Introduction to the ANS and Higher-Order Functions Somatic Nervous System (SNS) Operates under conscious control Seldom affects long-term survival SNS controls skeletal muscles Autonomic Nervous System (ANS) Operates without conscious instruction ANS controls visceral effectors Coordinates system functions Cardiovascular, respiratory, digestive, urinary, reproductive
3
4 Figure 16-1 An Overview of Neural Integration OVERVIEW OF NEURAL INTEGRATION CHAPTER 15 CHAPTER 16 Sensory processing centers in brain Sensory pathways Conscious and subconscious motor centers in brain Motor pathways Higher-Order Functions Memory, learning, and intelligence may influence interpretation of sensory information and nature of motor activities Somatic Nervous System (SNS) Autonomic Nervous System (ANS) General sensory receptors Skeletal muscles Visceral effectors (examples: smooth muscle, glands, cardiac muscle, adipocytes)
5 16-1 Autonomic Nervous System Organization of the ANS Integrative centers For autonomic activity in hypothalamus Neurons comparable to upper motor neurons in SNS
6 Figure 16-2a The Organization of the Somatic and Autonomic Nervous Systems Upper motor neurons in primary motor cortex Somatic motor nuclei of brain stem BRAIN Skeletal muscle Lower motor neurons SPINAL CORD Somatic motor nuclei of spinal cord Skeletal muscle Somatic nervous system
7 16-1 Autonomic Nervous System Organization of the ANS Visceral motor neurons In brain stem and spinal cord, are known as preganglionic neurons Autonomic ganglia Contain many ganglionic neurons Ganglionic neurons innervate visceral effectors Such as cardiac muscle, smooth muscle, glands, and adipose tissue
8 Figure 16-2b The Organization of the Somatic and Autonomic Nervous Systems Visceral motor nuclei in hypothalamus Preganglionic neuron Visceral Effectors BRAIN Smooth muscle Glands Cardiac muscle Adipocytes Ganglionic neurons Autonomic ganglia Preganglionic neurons Autonomic nuclei in brain stem SPINAL CORD Autonomic nuclei in spinal cord Autonomic nervous system
9 16-1 Divisions of the ANS The Autonomic Nervous System Operates largely outside our awareness Has two divisions 1. Sympathetic division Increases alertness, metabolic rate, and muscular abilities 2. Parasympathetic division Reduces metabolic rate and promotes digestion
10 16-1 Divisions of the ANS Sympathetic Division Kicks in only during exertion, stress, or emergency Fight or flight Parasympathetic Division Controls during resting conditions Rest and digest
11 16-1 Divisions of the ANS Sympathetic and Parasympathetic Division 1. Most often, these two divisions have opposing effects If the sympathetic division causes excitation, the parasympathetic causes inhibition 2. The two divisions may also work independently Only one division innervates some structures 3. The two divisions may work together, with each controlling one stage of a complex process
12 16-1 Divisions of the ANS Sympathetic Division Prepares body for crisis, producing a fight or flight response Stimulates tissue metabolism Increases alertness
13 The sympathetic nervous system prepares the body for situations requiring alertness or strength, or situations that arouse fear, anger, excitement, or embarrassment ( fight-or-flight situations). In these kinds of situations, the sympathetic nervous system stimulates cardiac muscles to increase the heart rate, causes dilation of the bronchioles of the lungs (increasing oxygen intake), and causes dilation of blood vessels that supply the heart and skeletal muscles (increasing blood supply). The adrenal medulla is stimulated to release epinephrine (adrenalin) and norepinephrine (noradrenalin), which in turn increases the metabolic rate of cells and stimulates the liver to release glucose into the blood. Sweat glands are stimulated to produce sweat. In addition, the sympathetic nervous system reduces the activity of various tranquil body functions, such as digestion and kidney functioning.
14 16-1 Divisions of the ANS Seven Responses to Increased Sympathetic Activity 1. Heightened mental alertness 2. Increased metabolic rate 3. Reduced digestive and urinary functions 4. Energy reserves activated 5. Increased respiratory rate and respiratory passageways dilate 6. Increased heart rate and blood pressure 7. Sweat glands activated
15 16-2 The Sympathetic Division Ganglionic Neurons Occur in three locations 1. Sympathetic chain ganglia (Visceral effectors in thoracic cavity, head, body wall, and limbs) 2. Collateral ganglia (Visceral effectors in abdominopelvic cavity) 3. Adrenal Medulla (Organs and systems throughout body)
16 Figure 16-3 The Organization of the Sympathetic Division of the ANS Sympathetic Division of ANS KEY Preganglionic Neurons Lateral gray horns of spinal segments T 1 L 2 Preganglionic fibers Ganglionic Neurons Sympathetic chain ganglia Collateral ganglia Adrenal medullae Target Organs Visceral effectors in thoracic cavity, head, body wall, and limbs Visceral effectors in abdominopelvic cavity Organs and systems throughout body Postganglionic fibers Hormones released into circulation
17 16-2 The Sympathetic Division Adrenal Medullae (Suprarenal Medullae) When stimulated, release neurotransmitters into bloodstream (not at synapse) Function as hormones to affect target cells throughout body
18 Figure 16-4c Sites of Ganglia in Sympathetic Pathways THE ADRENAL MEDULLAE Preganglionic fibers Endocrine cells (specialized ganglionic neurons) Adrenal medullae KEY Preganglionic neurons Ganglionic neurons Secretes neurotransmitters into general circulation
19 16-2 The Sympathetic Division Adrenal Medullae Neuroendocrine cells Secrete neurotransmitters epinephrine (E) and norepinephrine (NE) Epinephrine Also called adrenaline Is 75 80% of secretory output Remaining is norepinephrine (NE) Noradrenaline
20 16-2 The Sympathetic Division Adrenal Medullae Bloodstream carries neurotransmitters through body Causing changes in metabolic activities of different cells including cells not innervated by sympathetic postganglionic fibers Effects last longer Hormones continue to diffuse out of bloodstream
21 16-2 The Sympathetic Division Sympathetic Activation Change activities of tissues and organs by: Releasing NE at peripheral synapses Target specific effectors, smooth muscle fibers in blood vessels of skin Are activated in reflexes Do not involve other visceral effectors
22 16-2 The Sympathetic Division Sympathetic Activation Changes activities of tissues and organs by: Distributing E and NE throughout body in bloodstream Entire division responds (sympathetic activation) Are controlled by sympathetic centers in hypothalamus Effects are not limited to peripheral tissues Alters CNS activity
23 16-2 The Sympathetic Division Changes Caused by Sympathetic Activation Increased alertness Feelings of energy and euphoria Change in breathing Elevation in muscle tone Mobilization of energy reserves
24 16-3 Various Sympathetic Neurotransmitters Sympathetic Stimulation and the Release of NE and E Primarily from interactions of NE and E with two types of adrenergic membrane receptors 1. Alpha receptors (NE more potent) 2. Beta receptors Roles in circulation: E reacts with both α- and β receptors, causing vasoconstriction and vasodilation, respectively. Although α receptors are less sensitive to E, when activated, they override the vasodilation mediated by β- receptors. The result is that high levels of circulating E cause vasoconstriction. At lower levels of circulating epinephrine, β receptor stimulation dominates, producing an overall vasodilation. NE increases blood pressure through α- receptor activation.
25 16-1 Divisions of the ANS Parasympathetic Division Parasympathetic division stimulates visceral activity Conserves energy and promotes sedentary activities
26 The parasympathetic nervous system is active during periods of digestion and rest. It stimulates the production of digestive enzymes and stimulates the processes of digestion, urination, and defecation. It reduces blood pressure and heart and respiratory rates and conserves energy through relaxation and rest.
27 16-1 Divisions of the ANS Five Responses to Increased Parasympathetic Activity 1. Decreased metabolic rate 2. Decreased heart rate and blood pressure 3. Increased secretion by salivary and digestive glands 4. Increased motility and blood flow in digestive tract 5. Urination and defecation stimulation
28 16-4 The Parasympathetic Division Organization and Anatomy of the Parasympathetic Division Parasympathetic preganglionic fibers leave brain as components of cranial nerves III (oculomotor) VII (facial) IX (glossopharyngeal) X (vagus) Parasympathetic preganglionic fibers leave spinal cord at sacral level
29 Figure 16-7 The Organization of the Parasympathetic Division of the ANS Parasympathetic Division of ANS Preganglionic Neurons Nuclei in brain stem N III N VII Ganglionic Neurons Ciliary ganglion Target Organs Intrinsic eye muscles (pupil and lens shape) N IX Pterygopalatine and submandibular ganglia Nasal glands, tear glands, and salivary glands N X Otic ganglion Parotid salivary gland Intramural ganglia Visceral organs of neck, thoracic cavity, and most of abdominal cavity KEY Preganglionic fibers Postganglionic fibers Nuclei in spinal cord segments S 2 S 4 Pelvic nerves Intramural ganglia Visceral organs in inferior portion of abdominopelvic cavity
30 16-4 The Parasympathetic Division Oculomotor, Facial, and Glossopharyngeal Nerves Control visceral structures in head Synapse in ciliary, pterygopalatine, submandibular, and otic ganglia Short postganglionic fibers continue to their peripheral targets
31 16-4 The Parasympathetic Division Sacral Segments of Spinal Cord Preganglionic fibers carry sacral parasympathetic output Do not join ventral roots of spinal nerves, instead form pelvic nerves Pelvic nerves innervate intramural ganglia in walls of kidneys, urinary bladder, portions of large intestine, and the sex organs
32 Figure 16-8 The Distribution of Parasympathetic Innervation Pterygopalatine ganglion N III Lacrimal gland PONS N VII N IX Ciliary ganglion Submandibular ganglion Eye Salivary glands N X (Vagus) Otic ganglion Heart KEY Preganglionic neurons Ganglionic neurons Lungs
33 Figure 16-8 The Distribution of Parasympathetic Innervation KEY Preganglionic neurons Ganglionic neurons Lungs Autonomic plexuses (see Figure 16-10) Liver and gallbladder Stomach Spleen Pancreas Pelvic nerves Large intestine Small intestine Rectum Spinal cord S 2 S 3 S 4 Kidney Uterus Ovary Penis Scrotum Urinary bladder
34 16-4 The Parasympathetic Division Parasympathetic Activation Centers on relaxation, food processing, and energy absorption Localized effects, last a few seconds at most
35 16-4 The Parasympathetic Division Major Effects of Parasympathetic Division Constriction of the pupils (To restrict the amount of light that enters the eyes) And focusing of the lenses of the eyes on nearby objects Secretion by digestive glands Including salivary glands, gastric glands, duodenal glands, intestinal glands, the pancreas (exocrine and endocrine), and the liver
36 16-4 The Parasympathetic Division Major Effects of Parasympathetic Division Secretion of hormones That promote the absorption and utilization of nutrients by peripheral cells Changes in blood flow and glandular activity Associated with sexual arousal Increase in smooth muscle activity Along the digestive tract
37 16-4 The Parasympathetic Division Major Effects of Parasympathetic Division Stimulation and coordination of defecation Contraction of the urinary bladder during urination Constriction of the respiratory passageways Reduction in heart rate and in the force of contraction
38 16-8 Higher-Order Functions Memory Fact memories Are specific bits of information Skill memories Learned motor behaviors Short-term memories Information that can be recalled immediately Long-term memories Memory consolidation conversion from short-term to long-term memory Two types of long-term memory 1. Secondary memories fade and require effort to recall 2. Tertiary memories are with you for life
39 Figure Memory Storage Repetition promotes retention Long-term Memory Sensory input Short-term Memory Consolidation Secondary Memory Tertiary Memory Cerebral cortex (fact memory) Cerebral cortex and cerebellar cortex (skill memory) Permanent loss due to neural fatigue, shock, interference by other stimuli Temporary loss Permanent loss
40 16-8 Higher-Order Functions Cerebral Cortex Stores long-term memories Conscious motor and sensory memories referred to association areas Occipital and temporal lobes Special portions crucial to memories of faces, voices, and words A specific neuron may be activated by combination of sensory stimuli associated with particular individual; called grandmother cells
41 16-8 Higher-Order Functions Cerebral Cortex Visual association area Auditory association area Speech center Frontal lobes Related information stored in other locations If storage area is damaged, memory will be incomplete
42 16-8 Higher-Order Functions Cellular Mechanisms of Memory Formation and Storage Involves anatomical and physiological changes in neurons and synapses Increased neurotransmitter release Facilitation at synapses Formation of additional synaptic connections
43 16-8 Higher-Order Functions Cellular Mechanisms of Memory Formation and Storage Drugs stimulate CNS Caffeine and nicotine are examples Enhance memory consolidation through facilitation
44 16-8 Higher-Order Functions Cellular Mechanisms of Memory Formation and Storage Drugs stimulate CNS NMDA (N-methyl D-aspartate) Receptors Chemically gated calcium channels Activated by neurotransmitter glutamate Gates open, calcium enters cell Blocking NMDA receptors in hippocampus prevents long-term memory formation
45 16-9 Brain Chemistry Brain Chemistry Changes in normal balance between two or more neurotransmitters can profoundly affect brain function
46 16-9 Brain Chemistry Huntington s Disease Destruction of ACh-secreting and GABA-secreting neurons in basal nuclei Symptoms appear as basal nuclei and frontal lobes slowly degenerate Difficulty controlling movements Intellectual abilities gradually decline
47 16-9 Brain Chemistry Lysergic Acid Diethylamide (LSD) Powerful hallucinogenic drug Activates serotonin receptors in brain stem, hypothalamus, and limbic system
48 16-9 Brain Chemistry Serotonin Compounds that enhance effects also produce hallucinations (LSD) Compounds that inhibit or block action cause severe depression and anxiety Variations in levels affect sensory interpretation and emotional states
49 16-9 Brain Chemistry Serotonin Fluoxetine (Prozac) Slows removal of serotonin at synapses Increases serotonin concentrations at postsynaptic membrane Classified as selective serotonin reuptake inhibitors (SSRIs) Other SSRIs Celexa, Luvox, Paxil, and Zoloft
50 16-9 Brain Chemistry Parkinson s Disease Inadequate dopamine production causes motor problems Dopamine Secretion stimulated by amphetamines, or speed Large doses can produce symptoms resembling schizophrenia Important in nuclei that control intentional movements Important in other centers of diencephalon and cerebrum
51 16-10 Effects of Aging on the Nervous System Effects of Aging Anatomical and physiological changes begin after maturity (age 30) Accumulate over time 85% of people over age 65 have changes in mental performance and CNS function
52 16-10 Effects of Aging on the Nervous System Common Age-related Anatomical Changes in the Nervous System Reduction in Brain Size and Weight Reduction in Number of Neurons Decrease in Blood Flow to Brain Changes in Synaptic Organization of Brain Intracellular and Extracellular Changes in CNS Neurons
53 16-10 Effects of Aging on the Nervous System Reduction in Brain Size and Weight Decrease in volume of cerebral cortex Narrower gyri and wider sulci Larger subarachnoid space Reduction in Number of Neurons Brain shrinkage linked to loss of cortical neurons No neuronal loss in brain stem nuclei
54 16-10 Effects of Aging on the Nervous System Decrease in Blood Flow to Brain Arteriosclerosis Fatty deposits in walls of blood vessels Reduces blood flow through arteries Increases chances of rupture Cerebrovascular accident (CVA), or stroke May damage surrounding neural tissue
55 16-10 Effects of Aging on the Nervous System Changes in Synaptic Organization of Brain Number of dendritic branches, spines, and interconnections decreases Synaptic connections lost Rate of neurotransmitter production declines
56 16-10 Effects of Aging on the Nervous System Anatomical Changes Linked to functional changes Neural processing becomes less efficient with age Memory consolidation more difficult Secondary memories harder to access
57 16-10 Effects of Aging on the Nervous System Sensory Systems Hearing, balance, vision, smell, and taste become less acute Reaction times slowed Reflexes weaken or disappear Motor Control Precision decreases Takes longer to perform
58 16-10 Effects of Aging on the Nervous System Incapacitation 85% of elderly population develops changes that do not interfere with abilities Some individuals become incapacitated by progressive CNS changes
59 16-10 Effects of Aging on the Nervous System Senility Also called senile dementia Degenerative changes Memory loss Anterograde amnesia (lose ability to store new memories) Emotional disturbances Alzheimer s disease is most common
60 16-10 Nervous System Integration The Nervous System Monitors all other systems Issues commands that adjust their activities Like conductor of orchestra
61 16-10 Nervous System Integration Neural Tissue Extremely delicate Extracellular environment must maintain homeostatic limits If regulatory mechanisms break down, neurological disorders appear
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