chapter 11: blood 11.1 the composition and functions of blood 11.2 the blood cells 11.3 platelets...
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Chapter 11: Blood
11.1 The Composition and Functions of Blood
11.2 The Blood Cells
11.3 Platelets and Hemostasis
11.4 Capillary Exchange
11.5 Blood Typing and Transfusions
11.6 Effects of Aging
11.1 The Composition and Functions of Blood Objectives: Describe, in general, the composition of
_________________________. Divide the ___________________ of blood
into three categories, and discuss each category.
Describe the composition of _____________ and the specific functions of the plasma proteins.
Composition of Blood
Plasma (55%) WBCs and blood ____________________…top
Buffy coat Thin, shiny layer in middle
Formed elements (45%) RBCs, heavier because of _______________ Percentage of blood attributed to formed
__________________ is called the hematocrit.
Function 1: Transport
Moves from _________________ to all organs. Picks up __________________ from lungs and
nutrients from digestive tract and transports these to tissues.
Picks up cellular __________________, such as carbon dioxide
Transports hormones and messenger chemicals for various organs and _______________.
Function 2: Defense
Defends against pathogens (_________________ and viruses).
Removes ______________ and dying cells Some WBCs can ‘eat’ ____________________. Blood clotting to prevent blood loss. (platelets and
plasma __________________)
Function 3: Regulation Regulate body temperature by picking up heat
from ___________________ muscles. Uses concentration gradient (________________
__________) to transfer heat to other parts of the body.
Salts and plasma proteins keep osmotic __________________ in normal range.
Buffers in the blood keep the pH relatively constant at ___________
Plasma Composition
92% is __________________. 8% remaining is salts (ions) and ______________
molecules. Small: Glucose, amino acids, ______________ Large: _________________ and plasma proteins.
Plasma Proteins Functions Made in __________________ Help ________________ the blood and maintain
pH (homeostasis) Albumins contribute to the osmotic
__________________. Antibodies made by WBCs help fight infection
(gamma globulins) Transport different molecules. Fibrinogen and prothrombin are necessary for
______________________.
11.2 The Blood Cells
Objectives: Explain the hematopoietic role of _________
_____________in the red bone marrow. Describe the structure, function, and life cycle
of ______________ blood cells and _______________ blood cells.
Production of RBCs
Hematopoiesis: Process by which formed ___________________ are made (RBCs)
Multipotent stem cells: red ________________ marrow cells that mature into all the various types of blood cells.
May be able to ________________________ the body’s tissues in the laboratory.
Red Blood Cells Structure
Small, bioconcave disks that lack a _________________ when mature
Function Transport _________________________
Life Cycle Live only about _______________ days Aka erythrocytes, formed from red bone marrow stem cells Erythropoietin: hormone that helps induce RBC production;
abused by athletes Macrophages in _______________ and spleen engulf and
‘eat’ RBCs
White Blood Cells Structure
Larger, have a nucleus, lack hemoglobin, and are ___________________
Function Fight infection, destroy dead or dying body cells, and
recognize and kill ____________________ cells…all this helps maintain homeostasis
Life Cycle Produced by red bone marrow, can be found in tissue fluid
and ___________________ Many live only a few days when they fight infection Others live months or __________________
11.3 Platelets and Hemostasis
Objectives: Describe the structure, function, and life cycle
of _____________________. Describe the ______________ events of
hemostasis and the reactions necessary to coagulation.
Discuss __________________ of hemostasis.
Platelets
Structure ____________________________; fragmented from
megakaryocytes that develop in the red bone marrow Function
Necessary for hemostasis _______________________________________
Life Cycle Because they have no nucleus, they last at most
_____________ days
Hemostasis Vascular Spasm
Constriction of _________________ muscle layer in a broken blood vessel is the immediate response to injury
Platelets ______________________ seratonin that prolongs smooth muscle contraction
Platelet __________________________ Formation Platelets adhere to _____________________________ fibers that
are exposed when blood vessels break As platelets build up, a platelet plug forms
Coagulation Blood _____________________ Fibrinogen and prothrombin participate in blood clotting
Coagulation Requires protein clotting __________________; most
produced by liver Intrinsic mechanism: blood will coagulate in a
____________________________________ Extrinsic mechanism: activated when
______________ tissues release tissue thromboplastin Four steps: 1) Prothrombin activator is formed. 2)
Prothrombin activator converts prothrombin to thrombin. 3) Thrombin severs two short amino acid chains from each fibrinogen molecules; they join end-to-end, forming fibrin. 4) Fibrin threads wind around the platelet plug in the damaged area of the blood vessel and provide framework for clot.
Hemostasis Disorders Thrombocytopenia
__________________ platelet count autoimmune; your antibodies ________________
platelets Megakaryocytes in red bone marrow are destroyed
Hemophilia _______________________ (inherited) Deficiencies of clotting factors Hemophilia A: lack clotting factor _____________ and
is most severe
11.4 Capillary Exchange Objectives: Describe capillary _______________ within
the tissues.
Oxygen and nutrients leave a capillary. Cellular _______________ (carbon dioxide) enter the capillary.
In the lungs, it’s reversed. ______________ enters the blood and carbon dioxide leaves.
11.5 Blood Typing and Transfusions
Objectives: Explain the ______________ and Rh systems of
blood typing. Explain agglutination and its relationship to
__________________________.
ABO Blood Groups + Rh Factor
Type A and B blood are _____________________.
Type O blood is recessive. Rh positive is dominant and
Rh negative is ___________________.
Transfusions Agglutination: __________________ of RBCs Happens when transfusions are not
_______________________.
11.6 Effects of Aging Objectives: Name the blood ___________________ that are
commonly seen as we age.
Anemias, leukemias, and clotting disorders. _______________ deficiency anemia and pernicious
anemia (B12 deficient). Leukemia is ________________ that is genetic and
environmental. Thromboembolism occurs because arteries contain
________________________.