CoverModule 1.0. Homeostasis, Membranes, Electrophysiology and ANS (Essay Questions)1.1. Homeostasis1.1.1. Homeostasis Defined1.1.2. Homeostatic Control Systems1.1.3. Feedback Response Loop1.2. Cell Transport; Water & Solutes1.2.1. Fluid Compartments1.2.2. Osmosis1.2.3. Diffusion of Solutes1.2.4. Active Transport1.2.5. Bulk Transport1.3. Electrophysiology1.3.1. Ions and Cell Membranes1.3.2. Membrane Potentials1.3.3. Graded Potential1.3.4. Action Potentials1.3.5. Refractory Periods1.3.6. Propagation of an Action Potential1.4. THE SYNAPSE1.5. THE AUTONOMIC NERVOUS SYSTEM1.5.1. Organization of the Nervous System1.5.2. Structural Organization of the ANS1.5.3. The SNS and the PNS1.5.4. The Enteric Nervous System1.5.5. Physiology of the ANS1.5.6. Neurotransmitters of the ANS1.5.7. Receptors of the ANS1.5.8. Actions of the Autonomic Nervous System1.5.9. Table of Actions for the SNS and PNS and Some Common DrugsModule 2.0. Skeletal Muscle and Special Senses2.1. Structural Organization of Skeletal Muscle2.2.1. Neuromuscular Junction, Excitation-Contraction Coupling2.2.2. Muscle Contractures and Cramps2.3. Whole Muscle Contraction, Fiber Type, Fatigue and Muscle Pharmacology2.3.1. Motor Units2.3.2. Factors that Influence the Force of Contraction2.3.3. Energy Source for Muscle Contraction2.3.4. Skeletal Muscle Fiber Types2.3.5. Fatigue2.3.6. Muscle Pharmacology2.4. Smooth Muscle2.4.1. Smooth Muscle Contraction2.5. Control of Body Movement2.5.1. Voluntary Control of Muscle2.5.2. Reflexes2.6. Taste and Smell2.6.1. Taste2.6.2. The Sense of Smell2.7. Vision2.7.1. Structure of the Eye2.7.2. Focusing Light on the Retina2.7.3. Converting Light to Action Potentials2.7.4. The Retina2.7.5. Phototransduction2.7.6. Receptive Fields2.8. Hearing and Equilibrium2.8.1. The Nature of Sound2.8.2. The Hearing Apparatus2.8.3. Sound Vibrations to Action Potentials2.8.4. The Sense of Balance and EquilibriumModule 3.0. Cardiovascular System3.1. Structure of the Heart3.1.1. Chambers and Circulation3.2. Cardiac Cell Action Potentials3.2.1. Action Potentials in Cardiac Muscle Cells3.2.2. Action Potentials in Cardiac Autorhythmic cells3.2.3. Cellular Mechanisms of Inotropy and Chronotropy3.3. Electrophysiology of Heart Muscle3.3.1. Heart Conduction System3.3.2. Electrocardiogram (ECG)3.3.3. Abnormal ECG - Current of Injury3.4. The Cardiac Cycle3.4.1. Cardiac cycle3.4.2. Cardiac Measurements and Pressure Volume Loops3.5. Blood vessels and Blood Pressure3.5.1. Arteries and Veins3.5.2. Capillaries3.5.3. Blood Pressure Regulation and Shock3.5.4. Capillary Exchange3.5.5. Myogenic and Paracrine Regulation of Vasoconstriction and Vasodilation3.6. Blood3.6.1. Composition of Blood3.6.2. Hematopoeisis3.6.3. Breaking Down Red Blood Cells3.6.4. HemostasisModule 4.0. Urinary and Respiratory Systems4.1. Function and Structure of the Kidney4.1.1. Urinary System Function4.1.2. Functional Anatomy of the Urinary System4.1.3. The Nephron: Functional Unit of the Kidney4.1.4. The Renal Corpuscle: Bowman's Capsule4.2. Physiology of Urine Production4.2.1. Filtration4.2.2. Renal Clearance4.2.3. Tubular Reabsorption4.2.4. Urine Concentration and Dilution4.2.5. Hormonal Regulation of Urine Production4.3. Acid/Base Balance4.3.1. Buffers4.3.2. Acid/Base Disturbances4.4. The Respiratory System4.4.1. Respiratory System Structure and Function4.4.2. Respiratory Membrane4.4.3. Respiratory pressures and Inspriation/Expiration4.4.4. Alveoli and Surfactant4.4.5. Pneumothorax4.5. Gas Exchange and Transport4.5.1. Gas Laws4.5.2. Partial Pressure Gradients in the Lung4.5.3. Alveolar Gas Equation4.5.4. Oxygen and Carbon Dioxide Transport in the Blood4.5.5. Alveolar Ventilation4.5.6. Ventilation/Perfusion Ratio4.6. Chronic Bronchitis and Emphysema4.6.1. Respiratory Control by the Medulla Oblongata4.6.2. Chemicals that Regulate VentilationModule 5.0. Digestive, Endocrine and Reproductive Systems5.1. Functional Anatomy of the Digestive System5.1.1. Layers of the Digestive Tract5.1.2. Enteric Nervous System5.1.3. Organs of the Digestive System5.2. Digestion5.2.1. Carbohydrates5.2.2. Proteins5.2.3. Lipids5.2.4. Lipoproteins5.3. Regulation of Digestive Secretions5.4. Endocrine System5.4.1. Overview of the Endocrine System5.4.2. Hormone Receptors5.4.3. Hormones of the Body5.4.4. Other Hormones: Melatonin and Pheromones5.5. The Hypothalamus and Pituitary Gland5.5.1. Structure and Function of the Hypothalamus and Pituitary Gland5.5.2. The Posterior Pituitary5.5.3. The Anterior Pituitary5.5.4. Growth Hormone5.5.5. Prolactin5.5.6. Thyroid Hormones5.5.7. Adrenal Hormones5.6. Pancreas5.6.1. Insulin and Glucagon5.6.2. Diabetes Mellitus5.7. Reproductive System Anatomy5.7.1. Female Reproductive Anatomy5.7.2. Male Reproductive Anatomy5.7.3. Sexual Development at Puberty5.7.4. Male Reproductive Endocrine Axis5.7.5. Spermatogenesis5.7.6. Female Reproductive System: Oogenesis5.7.7. Ovulation and Fertilization5.7.8. The Ovarian Cycle5.7.9. The Uterine Cycle5.7.10. PregnancyAppendix A. GenderAppendix B. The Placebo EffectB.2.1. The Placebo EffectB.2.2. Examples of the Placebo EffectB.2.3. How do Placebos Work?B.2.4. Are Placebos Ethical?B.2.5. How do we validate actual effectiveness of placebosB.2.6. Tips for evaluating scientific evidenceB.2.7. What about Faith Healings
2.7.4

The Retina

The structure of the eye responsible for converting light waves into action potentials is the retina. The neural layer of the retina is composed of three main types of cells: the photoreceptors, the bipolar neurons and the ganglion cells. The photoreceptors, as the name implies, have the responsibility of capturing the light and converting it to an electrical signal. There are two types of photoreceptors in the retina, the rods and the cones. The rods see only in black and white and are mainly responsible for our night vision. The cones, on the other hand, can see in color and are responsible for color vision as well as sharp vision. Each eye contains about 120,000,000 rods and 6,000,000 cones. Although they detect light of different wavelengths, structurally, rods and cones are similar. They are composed of an outer segment that touches the pigment epithelium and is composed of numerous flattened discs stacked on each other (think of a stack of dinner plates). The only difference is that in the rods, all of the discs are the same size while in the cones they gradually decrease in diameter as they move to the end of the cell. This results in the shape for which the cones were named. The outer segment connects to the inner segment which houses the nucleus and other organelles of the cell. The inner segment, in turn connects to the synaptic terminal which forms the connection between the photoreceptor and the bipolar neuron (see the images below).

image073.jpg
Image by BYU-I Becky T. W18

The bipolar neurons, so named because they have one dendrite and one axon, are the connections between the photoreceptors and the ganglion cells. The axons of the ganglion cells form the optic nerve which exits the eye via the optic nerve. Two other cell types are shown in the image above. The horizontal cells can be seen in the layer where the photoreceptors synapse with the bipolar neurons and the Amacrine cells can be seen in the layer where the bipolar cells synapse with the ganglion cells. These two cells are involved in modulating the visual signals.

The distribution of the photoreceptors in the retina is not uniform. In the fovea centralis we find only cones. Moving more out from the fovea we start to see rods intermixed with the cones. The further out from the fovea we move the greater the number of rods and the fewer the number of cones.

In the image above note that the photoreceptors are located at the back of the retina. Light entering the eye must pass through the ganglion cells and the bipolar neurons before it gets to the photoreceptors. This doesn’t seem to be the best arrangement. However, at the fovea, the ganglion cells and the bipolar neurons radiate away from the cones in the fovea. Think of the crown of your head. All of the hairs radiate out from this point exposing the scalp. Because of this arrangement light striking the fovea has direct access to the photoreceptors, enhancing vision in this region of the retina.

Now let’s examine the unique characteristics of the different photoreceptors, starting with the rods. The rods are very sensitive to light and will respond to a single photon of light. In addition, they are part of convergent circuits in which several rods will converge on a single bipolar neuron and several bipolar neurons will converge on one ganglion cell. This allows for the summation of signals from several rods resulting in an action potential being sent to the brain. These properties make the rods ideal for seeing in very dim light, therefore rods are responsible for our night vision. During the day when there is plenty of light, the rods are essentially inactivated due to a process called bleaching (more on this later). You are aware of how hard it is to see in a darkened theater when you first enter from bright light. After you have been there for a while and the rods become active we can see quite well in the room. Indeed, after about 40 minutes in the dark room our eyes are about 25,000 times more sensitive than they were when we first entered the room. There are two downsides to the use of rods, however. First, they do not see in color, rods see only in black and white. Second, due to the convergence their visual fields are quite large. Light striking any of the rods that converge on one ganglion cell will produce the same “pixel.” Therefore, vision with rods is very sensitive but not very acute (sharp). Cones, on the other hand, have essentially the opposite characteristics. First, there is very little convergence in their circuitry. Light striking two cones located next to each other would produce two different pixels in the brain. This allows for very sharp (acute) vision for images striking the fovea since there are only cones in the fovea. Second, the cones are much less sensitive than rods. At night, the intensity of light usually is not sufficient to stimulate the cones. Third, the cones are responsible for our color vision. We have three types of cones that respond to light in the red, green or blue wavelengths. By mixing the input from these three cones, humans can perceive about 1,000,000 different hues of color. You may know someone who is “color blind.” Color blindness is most often due to a genetic condition where the subject does not produce one or more of the cones. The most common condition is red-green colorblindness, where the person lacks either the red or green cone. Individuals with this condition can see colors, but they have a difficult time distinguishing between shades of green and red. The genes for the green and red cones are found on the X chromosome, therefore males have a much higher incidence of color blindness since males only have one X chromosome. Women have two X chromosomes so even if they inherit a defective gene there is a good chance the gene on the other X chromosome will be normal. For a women to be red-green colorblind, both her father and her mother would have to have the condition. Another type of color blindness called Blue-yellow color blindness involves genes for the blue cones, but these genes are not on the X chromosome so it occurs at the same rate in both males and females.

End-of-Chapter Survey

: How would you rate the overall quality of this chapter?
  1. Very Low Quality
  2. Low Quality
  3. Moderate Quality
  4. High Quality
  5. Very High Quality
Comments will be automatically submitted when you navigate away from the page.