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A&P 2 Test 5
| Question | Answer |
|---|---|
| There is a higher composition of plasma proteins in __________ than there are in lymph and interstitial fluid. | plasma |
| _________ is clear, watery-appearing fluid found in the lymphatic vessels that is isotonic. | Lymph (or lymphatic fluid) |
| ________ _________ fills spaces between cells. Has a lower protein concentration. | Interstitial fluid |
| Both lymph and interstitial fluid closely resemble _______ __________ in composition. | blood plasma |
| Lymph and interstitial fluid contain a lower percentage of _______ than plasma | proteins |
| The average concentration of protein (4 grams/100 ml) in lymph taken from the ______ _______ is about twice that found in most interstitial fluid samples. | thoracic duct |
| Lymph is isotonic and almost identical in chemical composition to _______ _______ when comparisons are made between the two fluids taken from the same area of the body | interstitial fluid |
| Lymph from the __________ _________ ____________ empties into the right lymphatic duct and then into the right subclavian vein. | upper right quadrant |
| Lymph from the rest of the body empties into the ___________ duct and left subclavian vein. | thoracic |
| __________ are lymphatic capillaries in the villi found in the small intestines. | Lacteals |
| Lacteals absorb fats and other nutrients from the _________ _________ | small intestines |
| The milky lymph found in lacteals after digestion contains 1% to 2% fat and is called ________ | chyle |
| Interstitial fluid has much (lower/higher) lipid content than chyle. | lower |
| Lymphatics have (thinner/thicker) walls than veins | thinner |
| Lymphatics contain more _______ than veins | valves |
| Lymphatics contain ________ __________ located at certain intervals along their course | lymph nodes |
| The importance of the lymphatic system is maintaining a balance of fluid in the __________ environment. | internal |
| ___________ filters into interstitial spaces from blood flowing through capillaries | Plasma |
| Most ________ __________ is absorbed by tissue cells or reabsorbed by the blood before it flows out of the tissue. | Interstitial fluid (IF) |
| Where does the small percentage of the interstitial fluid left behind go? | It remains behind |
| __________ ____________ act as “drains” to collect the excess tissue fluid and return it to the venous blood just before it reaches the heart. | lymphatic vessels |
| The ____________ system maintains includes immunity. Note: Maintains fluid balance in the internal environment | lymphatic |
| __________ could cause tissue destruction | Edema |
| The __________ system is involved in immunity. | lymphatic |
| __________ ___________ are lymph organs that collect fluids draining from tissues of the body (lymph) and return it to the blood circulation | lymphatic vessels |
| ________ __________ are lymph organs that collect tissue fluid (forming lymph) & transport lymph to larger lymphatic vessels. | lymphatic capillaries |
| ________ ________ are lymph organs that collect lymph from network of lymphatic vessels and drain it into the blood circulation | Lymphatic ducts |
| __________ _________ are responsible for Hematopoiesis (WBCs), immunity, filter body fluids | Lymphoid organs |
| _______ ______ are lymph organs that are responsible for filtration of lymph before it enters bloodstream; mechanical filtration: removing particles; biological filtration: cells destroy and remove particles | lymph nodes |
| _________ _________ _________ are lymph organs that are responsible for immunity at common points of entry for pathogenic microbes | Aggregated lymph nodules (tonsils, Peyer patches) |
| The _________ is a lymph organ responsible for hematopoiesis--site of T-lymphocyte (T-cell) development; hormone production—thymosin regulates T-cell development | Thymus |
| The___________ is a lymph organ responsible for hematopoiesis (WBCs), Immunity, filtration of blood, tissue repairs, destruction of old RBCs & platelets, and blood reservoir | Spleen |
| The ____________ is the primary organ of the lymphatic system and it is an unpaired organ made up of two pyramidal lobes located in the mediastinum. | thymus |
| With advancing age, the thymus becomes yellowish as lymphoid tissue is replaced by _____. | fat |
| Lymph that empties into the right lymphatic ducts, then drains into the ______ ________ _______ | right subclavian vein |
| Lymph that empties into the thoracic duct, then drains into the _______ ______ _______ | left subclavian vein |
| Once the lymph drains into the left subclavian vein it joins the left ______ _______ _______ | internal jugular vein |
| In most people there are __________ separate lymphatic ducts that drain into the right subclavian vein rather than a single right lymphatic duct. | three |
| Lymph pressure gradient is established by the rise of ________ ___________ pressure | Interstitial fluid (IF) |
| Increased ________ ________ can increase IF pressure | muscle movement |
| Accumulation of additional interstitial fluid volume within _______ can increase IF pressure. | tissue |
| Process of __________ establishes a fluid pressure gradient for lymph. | inspiration |
| _________ _________ __________ increase lymph flow | Skeletal muscle contractions |
| Total volume of lymph depends on _________ of inspiration. | depth |
| Lymph entrance and return rates vary because it is _________________ on the amount of physical activity and other factors. | dependent |
| Studies have shown that thoracic duct lymph is literally “___________” into the venous system during the inspiration phase of pulmonary ventilation. | pumped |
| As muscles contract, they “_______” the lymphatic vessels and push the lymph forward. | milk |
| The actual pressure generated in the system remains very ________, and movement of lymph proceeds quite _________ compared to the circulation of blood. | low, slowly |
| ________ _________ and _________ ____________ __________ contribute to the blood pressure gradient in veins and also establish a lymph pressure gradient. | breathing movements and skeletal muscle contractions |
| _________________ is an abnormal condition in which swelling of tissues in the extremities occurs because of an obstruction of the lymphatics and the accumulation of lymph. | Lymphadema |
| _________________ develops when the blockage and edema become so severe that the affected extremities resemble an elephant’s limbs. | Elephantitis |
| Lymph circulation is maintained as it moves through the system in the right direction because of the large number of __________ that permit fluid flow only in the central direction | valves |
| A lymph node is roughly _____-_____ mm. | 1-20 mm |
| Activities that result in central movement, or flow, of lymph are called ________________ actions | lymphokinetic |
| Examples of such ________________ factors include interstitial fluid pressure, arterial pulsations, postural changes, and passive compression (massage) of the body soft tissues. | lymphokinetic |
| ______________ is the movement (flow) of lymph. | Lymphokinesis |
| The two functions of the lymph nodes are __________ and ____________. | defense and hematopoiesis. |
| _________ includes mechanical filtration stopping particles from passing any further in the body. Also is biological filtration the use of phagocytosis to destroy particles. | Defense |
| Lymph nodes serve as the site of the final stages of maturation for some types of ___________ and __________ that have migrated from bone marrow. | lymphocytes and monocytes |
| Most lymph nodes occur in __________, or ________ | groups, or clusters |
| ___________ Lymph Nodes are located just in front of the ear; these nodes drain the superficial tissues and skin on the lateral side of the head and face | Preauricular |
| _________ Group & ______________ Group (Submaxillary) lymph nodes are in the floor of the mouth; lymph from the nose, lips, and teeth drains through these nodes | Submental Group & Submandibular Group (Submaxillary): |
| __________ __________ Lymph Nodes are in the neck along the sternocleidomastoid muscle, these nodes drain lymph (which has already passed through other nodes) from the head and neck | Superficial Cervical |
| ___________ ___________ Lymph Nodes (Supratrochlear Lymph Nodes): Located just above the bend of the elbow; lymph from the forearm passes through these nodes | Superficial Cubital |
| ___________ Lymph Nodes are 20 to 30 large nodes clustered deep within the underarm and upper chest regions; lymph from the arm and upper part of the thoracic wall, including the breast, drains through these nodes | Axillary |
| ________ Lymph Nodes and _______ Lymph Nodes are in the pelvis and groin; lymph from the pelvic organs, legs, and external genitals drains through these nodes | Iliac Lymph Nodes and Inguinal Lymph Nodes |
| Preauriclar=________ | ear |
| SubMen/SubMan/SubMax = _________ | Mouth |
| Cervical = _______ | Neck |
| Cubital = __________ | Elbow |
| Axillary = ________ | Armpits |
| Inguinal = ________ | Groin |
| _______ are most numerous (or prevalent) phagocyte; usually first to arrive at site of injury; migrates out of bloodstream during diapedesis; forms pus; grandular WBCs | Neutrophils |
| _____________ meaning “large eater”) are phagocytic monocytes that have grown to several times their original size after migrating out of the bloodstream | Macrophages |
| Both _________ and _________ are a part of innate immune system. | Neutrophils and Macrophages |
| The lymphatic tissue of lymph nodes serves as the final maturation site for ___________ and ____________. | monocytes and lymphocytes. |
| _______ are granular leukocytes that are usually the first phagocytic cell to arrive at the scene of an inflammatory response. | Neutrophils |
| ________ are monocytes that have enlarged to become giant phagocytic cells capable of consuming many pathogens, often called by other, more specific names when found in specific tissues of the body. | Macrophages |
| Which one (neutrophils or monocytes) is produced by lymph nodes? | Monocytes are produced by lymph nodes. |
| More than ____% of the lymph from the breast enters the lymph nodes of the axillary region. Most of the remainder enters lymph nodes along the lateral edges of the sternum. | 85% |
| The breast has lymphatics that originate in and drain the skin ______the breast, except the areola and nipple, as well as lymphatics that originate in and drain the _________substance of the breast itself, as well as the skin of the areola and nipple | over, underlying |
| _______ ___________ has mechanisms that resist various threatening agents or conditions, not just certain specific agents. It kills everything and is very general. | Nonspecific immunity |
| Mechanical and chemical barriers, such as the skin & mucous membranes, are the body’s _______ _______ of defense. | first line |
| What are the four main inflammation mediators? | Histamine, Prostglandins, Kinins, and Leukotrienes |
| Most prevalent (or numerous) phagocyte? | Neutrophils |
| What are the 3 major types of interferon. | Immune, Leukocytes, and Fibroblasts |
| ________ is ingestion and destruction of microorganisms and small particles | Phagocytosis |
| After digestion, phagocyte proteins display bits of peptides on the surface that are later recognized by cells of the adaptive immune system as ________ | antigens |
| Phagocytosis is usually a part of _______ defense. | innate |
| Neutrophils (most numerous), Macrophage, Dendritic Cell are all ________ | Phagocytes |
| _______ inhibit the spread of viruses | Interferons |
| _________ are proteins synthesized and released into circulation by certain cells invaded by viruses to signal other nearby cells to enter a protective antiviral state | Interferons |
| Immune, Leukocytes, and Fibroblasts are examples of ____________ | interferons |
| What are all the cells that are involved in Nonspecific (Innate) Immunity? | Phagocytes (like Neutrophils, Macrophage, Dendritic), Complement enzymes, and Natural-Killer cells |
| _____________ is best described as an enzyme in the blood plasma. | Complement |
| Complements kill invading cells by drilling a hole in their ________ ___________. | plasma membrane |
| ____________ is a name given to about 20 inactive enzymes in the plasma on the cells surfaces. | Complement |
| Complements are triggered by _________ mechanisms-not a chemical barrier like hydrochloride acid or hydrolyzing enzymes. | immune |
| __________ is a normal mechanism that usually speeds up recovery from infection or injury usually showing signs of heat, redness, pain, and swelling. | Inflammation |
| ________ ________ elicits responses to counteract injury and promote a return to normal | Tissue damage |
| Many inflammation mediators are ___________ factors | chemotactic |
| _____________ promote prostaglandin production | Pyrogens |
| ________-________ is when the immune system attacks abnormal or foreign cells but spares the body’s own cells | Self-tolerance |
| _________ are molecules on the surface of foreign cells that are recognition markers | Nonself |
| _____________ is a substance that may be present to act as innate defense mechanism. First line of defense-mechanical and chemical barriers. | Sebum |
| Secretions such as sebum, mucus, acids, and enzymes ___________ inhibit the activity of pathogens | chemically |
| How can an enzyme destroy a pathogen? | Enzymes may hydrolyze pathogens. This is considered a chemical process. |
| How does hydrochloric acid play a role in immunity? | Hydrochloric Acid in gastric mucosa may destroy pathogens by lowering pH. |
| Look at and review #34 on the study guide | :) |
| How does a white blood cell ingests and destroys a microorganism? | They ingest and destroy by phagocytosis; they also release antibodies and antitoxins |
| _________ extend foot-like projections (pseudopods) toward microorganisms | Phagocytes |
| __________ encircle the microorganism in a phagosome | Pseudopods |
| ___________ drain the phagosome, which kills the microorganism | Lysosomes |
| _____________ activate complement after binding to an antigen by exposing complement-binding sites This triggers a cascade of reactions until each enzyme has functioned | Antibodies |
| ____________ is “cell bursting”; often occurs when ions and water rush into a cell, causing it to burst | Cytolysis |
| 2 year old female patient is battling leukemia. Unfortunately, she comes in contact with chicken pox. What would the oncologists do and why? | Due to her WBC being low from chemo, the oncologist would find some way to keep the disease from spreading and becoming infected. |
| B cell mechanisms are considered __________ _________ immunity. | antibody mediated |
| _____ cells produce antibodies that attack pathogens. | B cells |
| __________ are antigens that induce the immune system to make certain responses. | Macromolecules (large molecules_ |
| Many antigens that enter the body are macromolecules located in the walls or outer membranes of ______________ or the outer coats of ________. | microorganisms or viruses |
| ___________ are proteins that potentially trigger a specific immune response (macro molecules that induce the immune system to make certain responses) | Antigens |
| Most antigens are ________ _________ | foreign proteins |
| Each kind of antigen usually has specific and uniquely shaped ________ | epitopes |
| A ___________ ___________ survives for a long period in the lymph nodes and if later exposed to the same specific antigen, forms a clone of cells that rapidly produce a specific immune response. | memory cell |
| Memory cells become _______ _________ | plasma cells |
| Immunoglobulin ____ Makes up 75% of antibodies in the blood. * Most prevalent antibody * The predominant antibody of the secondary antibody response. | IgG |
| Immunoglobulin ______ is a major class of antibody in the mucous membranes, saliva, and tears | IgA |
| Immunoglobulin ____ is an antibody that naive B cells synthesize and insert into their own plasma membrane. * The predominant class produced after initial contact with an antigen | IgM |
| Immunoglobulin ___ is produced in small amount; produces harmful effects, such as allergies | IgE |
| Immunoglobulin ___ is found in small amounts in the blood; it's precise function is unknown. | IgD |
| _________ is a group of proteins that, when activated, work together to destroy foreign cells. | Complement |
| ________ immunity results from non-deliberate exposure to antigens | Natural |
| ________ immunity results from deliberate exposure to antigens | Artificial |
| ________ immunity is when the immune system responds to a harmful agent regardless of whether it was natural or artificial; lasts longer than passive immunity | Active |
| ________ immunity is when When immunity to a disease that developed in another individual or animal is transferred to an individual who was not previously immune; is temporary but provides immediate protection. | Passive |
| An example of passive immunity is _______-_______ | breast-feeding |
| Adaptive immunity is part of the ________ line of defense consisting of lymphocytes (White Blood Cells) | third |
| What are the two different classes of lymphocytes? | B-cells and T-cells |
| ____ cells produce antibodies that attack __________ | pathogens |
| _____ cell mechanisms attack pathogens more directly (cell-mediated immunity) | T cell |
| Activation of ____________ requires a specific antigen and a chemical signal | lymphocytes |
| A _______ is a compact form of DNA that exists only during cell division | Chromosome |
| A _______ is a strand form of DNA made up of subunits called nucleosomes | Chromatin |
| __________ are small spools of DNA wound around proteins called histones. | Nucleosomes |
| When its genetic codes are being expressed, DNA is in a threadlike form called ____________ | Chromatin |
| Each DNA molecule can be called either a _________ strand or a ___________, depending on the form it is in. | Chromatin strand or a chromosome |
| A ______ is when gametes produce only 23 chromosomes - exactly one half the original number. | Haploid |
| A _______ is when the 23 chromosomes from the ovum and the sperm unite at conception and make a zygote with 46 chromosomes. Thus the same number chromosomes as the parents | Diploid |
| ________ __________ happens when two members of a pair of homologous chromosome separate and then the maternal and paternal chromosomes get mixed up and distributed independently. | Independent assortment |
| independent assortment of chromosomes ensures that each offspring from a single set of parents is genetically _________ | unique |
| ________ __________ is when genes of an individual chromosome stay together | Genetic linkage |
| _______ ______ occurs when genes from one location cross to the same location on a matching chromosome | Crossing over |
| In ________ ________ genes from one chromosome are exchanged with matching genes in the other chromosome of a pairing during meiosis. | Crossing over |
| In _______ the enzyme tyrosinase is absent from birth because of a genetic mutation | albinism |
| In albinism the _________ cannot form melanin | melanocytes |
| Albino individuals have a characteristic absence of ____________ in their hair, skin, and eyes. | pigment |
| If both mom and dad give the recessive chromosome for albinism, the child (is/is not) albino | is |
| If mom gives an abnormal chromosome, and dad gives the normal chromosome for albinism, the child (is/is not) albino | is not, but a carrier |
| If mom gives normal chromosome, and dad gives normal chromosome form albinism (is/is not) albino. | is not |
| Recessive x-linked condition is red-green color blindness, which involves a deficiency of normal photopigments in the ___________. | retina |
| In red-green color blindness , male children of a parent who carries the recessive abnormal gene on an ______ chromosome may be color blind. | X chromosome |
| In red-green color blindness, a female can inherit this form of color blindness only if her (father/mother) is color blind and her (father/mother) is either color blind (homozygous recessive) or a color-blindness carrier (heterozygous). | father, mother |
| Male sex chromosome | XY |
| Female sex chromosomes | XX |
| Klinefelter's sex chromosomes | XXY |
| Turner's sex chromosomes | XO |
| Sickle cell trait provides ___________ to malaria. | resistance |
| Individuals who are heterozygous for sickle cells are (more/less) likely to survive and reproduce, spreading the abnormal gene further in the population | more |
| In ____________, recessive X-linked genes are masked by dominant genes in the other X chromosome. | females |
| In __________ inherit only one X chromosomes (from the mother), the presence of only one recessive X-linked genes is enough to produce the recessive trait. | males |
| Only females with ______ recessive X-linked genes can exhibit the recessive trait. | two |
| The X-linked recessive traits is more common in (males/females) | males |
| What is an example of the X-linked recessive traits? | red-green color blindness: a female carrier of the abnormal recessive gene on an X chromosome can produce male children who are color blind. |
| If a person is XXY (Trisomy), what are they diagnosed with and how would they present? | Klinefelter's syndrome: Occurs in males with a Y chromosome and at least two X chromosomes. They are always sterile, small testes, some development of breasts, long limb, low IQ. |
| If a person is XO (Monosomy), what are they diagnosed with and how would they present? | Turner’s syndrome: Occurs in females with only a X chromosome. They are always sterile, failure of ovaries and other organs would not mature, short in stature, webbed neck, learning disorders. |
| In Mitochondrial DNA, each __________ has its own DNA molecule | Mitochondrion |
| Inheritance of mtDNA occurs through the (mother/father) because sperm does not contribute mitochondria to the ovum during fertilization | mother |
| _______DNA contains the only genetic code for several important enzymes | Mitochondrial |
| _________ results from a mistake in meiosis called nondisjunction | Trisomy |
| ___________ is when a pair of chromosomes fails to separate. | Nondisjunction |
| Complete monosomy can occur because of meiotic nondisjunction, but only one complete monosomy (Turner syndrome) is viable in _________ | humans |
| _________ _______ results because of recessive genes in chromosome pair 7 | Cystic fibrosis |
| In ________ ________ Impairment of chloride ion transport across cell membranes causes exocrine cells to secrete a thick mucus and concentrated sweat (salty) | Cystic fibrosis |
| Thickened mucus may obstruct ___________ and ____________ tracts, leading to death | respiratory and gastrointestinal |
| Treatment for cystic fibrosis is _______ and other therapies. | drugs |
| Tay-Sachs Disease (TSD), Sickle Cell Anemia, Cystic Fibrosis, Phenylketonuria (PKU) are all disease that demonstrate a _________ gene inheritance and are _______ __________ | single, autosomal recessive |
| ____________ results from recessive genes that fail to produce phenylalanine hydroxylase | phenylketonuria or PKU |
| In PKU, Phenylalanine cannot be converted into ____________ and thus accumulates | tyrosine |
| High concentrations of phenylalanine destroy _______ _________ | brain tissue |
| Treatment of phenylketonuria includes what? | Diets low in phenylalanine |
| ________-_____________ disease is a recessive condition involving failure to make an essential lipid-processing enzyme | Tay-Sachs disease (TSD) |
| carrying one TSD gene may be protective against _____________ | tuberculosis (TB) |
| In _______ ________ disease, abnormal lipids accumulate in the brain, causing severe retardation and death by 4 years of age | Tay-Sachs disease (TSD) |
| TSD is predominant in the ____________ community | Jewish community |
| Is there any specific therapy available for Tay-Sachs disease? | No. |
| _________ is a chart that illustrates genetic relationships in a family over several generations; helpful in determining the possibility of producing offspring with certain genetic disorders | Pedigree |
| Using medical records and family histories, genetic counselors assemble the ___________ beginning with the client and moving backward through as many generations as are known. Squares represent males; circles represent females. | Pedigree |
| ________ __________ genes regulate cell division so it proceeds normally | Tumor suppressor genes |
| If a tumor suppressor gene is nonfunctional because of a genetic mutation, it allows cells to divide _____________. | abnormally |
| ________ _______________ attempts to add genetically altered cells to the body, rather than change existing body cells, as in gene replacement therapy. | Gene augmentation |
| Disorders that involve trisomy (extra chromosomes), monosomy (missing chromosomes), and broken chromosomes can be detected after a _____________ is produced | karyotype |
| The first step in producing a karyotype is getting a sample of ________ from the individual to be tested | cells |
| A _______ is ordered arrangement of photographs of chromosomes from a single cell. | Karyotype |