Human Physiology Flashcards
Structure of the digestive system, The blood system, Defence against infectious diseases, Gas exchange, Neurons and synapses, Hormones, homeostasis and reproduction
Outline the role of peristalsis in the digestive process
List the name, substrate and product of four pancreatic enzymes that hydrolyze food in the small intestine
List the name and substrate of the three major classes of enzymes secreted by the pancreas
List the name, substrate and product of six enzymes produced by gland cells in the small intestine wall
Describe why enzymes produced by gland cells in the small intestine wall often remain immobilized in the cell membrane
List three adaptations that increase the surface area for absorption on the small intestine
Draw the villi as viewed in cross section
Label the following on a diagram of a villi: capillary, epithelial cell, lacteal, and goblet cell
State the function of the following villi structures: capillary, epithelial cell, lacteal, and goblet cell
Define “absorption”
List materials absorbed by the villi cells of the small intestine
List four methods of membrane transport required to absorb nutrients
Describe the absorption of triglycerides
Describe the absorption of glucose
Describe the structure of starch
Outline the source, function and specificity of amylase
Outline the digestion of maltose, maltotriose and dextrins into glucose
Describe absorption of glucose by villus epithelial cells
State the role of the digestive system
Explain the use of dialysis tubing as a model for the small intestine
Describe transport of glucose into and through villi capillaries
Draw a diagram of the human digestive system
Outline the function of the following digestive system structures: mouth, esophagus, stomach, small intestine, pancreas, liver, gall bladder, and large intestine
Mouth:
Esophagus:
Stomach:
Small intestine:
Pancreas:
Liver:
Gall bladder:
Large intestine:
Outline the function of the four layers of tissue found in the wall of the small intestine
Explain the use of models in physiology research
Label the four layers of tissue found in the wall of the small intestine as viewed with a microscope or in a micrograph
State two examples of model systems used to study digestion
State limitations of using model systems in physiology research
State the function of arteries
Outline the role of elastic and muscle tissue in arteries
Describe the structure and function of the three layers of artery wall tissue
Describe the structure and function of capillaries
Describe the mechanism used to maintain blood flow in arteries between heartbeats
State the reason for toughness of artery walls
Define systolic and diastolic blood pressure
Define “vasoconstriction” and “vasodilation”
Vasoconstriction:
Vasodilation:
State the function of veins
Veins collect blood at low pressure from the tissues of the body and return it to the right atria of the heart.
Describe the cause and effect of diffusion of blood plasma into and out of a capillary network
Draw a diagram to illustrate the double circulation system in mammals
Outline the roles of gravity and skeletal muscle pressure in maintaining flow of blood through a vein
Outline the structure and function of a pocket valve
Compare the circulation of blood in fish to that of mammals
Explain the flow of blood through the pulmonary and systemic circulations
Outline the role of cells in the sinoatrial node
Explain why the mammalian heart must function as a double pump
Define “myogenic contraction”
Describe the propagation of the electrical signal from the sinoatrial node through the atria and ventricles
State the reason why the sinoatrial node is often called the pacemaker
Outline the structures and functions of nervous tissue that can regulate heart rate
Describe factors that will increase heart rate
Describe factors that will decrease heart rate
Outline conditions that will lead to epinephrine secretion
Explain the effect of epinephrine on heart rate
Describe the cause and consequence of atherosclerosis
Outline William Harvey’s role in discovery of blood circulation
Outline the effect of a coronary occlusion on heart function
Explain the pressure changes in the left atrium, left ventricle and aorta during the cardiac cycle
Explain the relationship between atrial and ventricular pressure and the opening and closing of heart valves
Explain the atrial, ventricular and arterial pressure changes as illustrated on a graph of pressure changes during the cardiac cycle
Identify the time of opening and closing of heart valves on a graph o f pressure changes during the cardiac cycle
Compare the diameter, relative wall thickness, lumen diameter, number of wall layers, abundance of muscle and elastic fibres and presence of valves in arteries, capillaries and veins
Given a micrograph, identify a blood vessel as an artery, capillary or vein
Label a diagram of the heart with the following structure names: superior vena cava, inferior vena cava, pulmonary semilunar valve, aorta, pulmonary artery, pulmonary veins, aortic semilunar valve, left atrioventricular valve, left ventricle, septum, right ventricle, left atrium, right atrium and right atrioventricular valve
Describe how Harvey was able to disprove Galen’s theory
Outline Galen’s description of blood flow in the body
Define “pathogen”
State that skin and mucous membranes form the first line of defense against pathogens
Outline the role of skin, sebaceous glands and mucous membranes in the defense against pathogens
Describe the blood clotting cascade, including the role of platelets, clotting factors, thrombin, fibrinogen and fibrin
State two benefits of blood clotting when skin is cut
Outline two roles of platelets in the blood clotting cascade.
State the white blood cells are the second line of defence against pathogens
Define “specific immune response”
Outline the function of phagocytic white blood cells in defense against pathogens
Contrast antigen and antibody
Antigen:
Antibody:
Describe the structure and function of antibodies
State the function of plasma cells and memory cells.
Explain why antibiotics are ineffective against viruses