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Understanding Pathophysiology 8TH Edition MCCANCE, HUETHER Test Bank

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TEST BANK FOR UNDERSTANDING PATHOPHYSIOLOGY 8TH EDITION MCCANCE, HUETHER MULTIPLE CHOICE 1. Which statement best describes the cellular function of metabolic absorption? a. Cells can produce proteins. c. Cells can take in and use nutrients. b. Cells can secrete digestive enzymes. d. Cells can synthesize fats. ANS: C In metabolic absorption, all cells take in and use nutrients and other substances from their surroundings. The remaining options are not inclusive in their descriptions of cellular metabolic absorption. PTS: 1 REF: Page 2 2. Most of a cell’s genetic information, including RNA and DNA, is contained in the: a. Mitochondria c. Nucleolus b. Ribosome d. Lysosome ANS: C The nucleus contains the nucleolus, a small dense structure composed largely of RNA, most of the cellular DNA, and the DNA-binding proteins, such as the histones, which regulate its activity. The other options do not contain most of a cell’s genetic information. PTS: 1 REF: Page 2 3. Which component of the cell produces hydrogen peroxide (H2O2) by using oxygen to remove hydrogen atoms from specific substrates in an oxidative reaction? a. Lysosomes c. Ribosomes b. Peroxisomes d. Oxyhydrosomes ANS: B Peroxisomes are so named because they usually contain enzymes that use oxygen to remove hydrogen atoms from specific substrates in an oxidative reaction that produces H2O2, which is a powerful oxidant and potentially destructive if it accumulates or escapes from peroxisomes. Ribosomes are RNA-protein complexes (nucleoproteins) that are synthesized in the nucleolus and secreted into the cytoplasm through pores in the nuclear envelope called nuclear pore complexes. Lysosomes are saclike structures that originate from the Golgi complex and contain more than 40 digestive enzymes called hydrolases, which catalyze bonds in proteins, lipids, nucleic acids, and carbohydrates. Oxyhydrosomes are involved in enzyme production. PTS: 1 REF: Page 8 4. Which cell component is capable of cellular autodigestion when it is released during cell injury? a. Ribosome c. Smooth endoplasmic reticulum b. Golgi complex d. Lysosomes ANS: D The lysosomal membrane acts as a protective shield between the powerful digestive enzymes within the lysosome and the cytoplasm, preventing their leakage into the cytoplasmic matrix. Disruption of the membrane by various treatments or cellular injury leads to a release of the lysosomal enzymes, which can then react with their specific substrates, causing cellular self-digestion. The other options do not correctly describe this process. PTS: 1 REF: Pages 7-8 5. What is the sequence of steps in the development of a digestive enzyme by the pancreas cells from the initial transcription to the release from the cell? a. The enzyme is transcribed from DNA by RNA in the nucleus, proceeds to the ribosome for synthesis, and is transported in a secretory vesicle to the cell membrane. b. The enzyme is transcribed from RNA by DNA in the nucleus, proceeds to the lysosome for synthesis, and is transported in an encapsulated membrane to the cell membrane. c. The enzyme is transcribed by the mitochondria in the nucleus, proceeds to the ribosome for synthesis, and is transported in a cytoskeleton to the cell membrane. d. The enzyme is transcribed from DNA by RNA in the nucleus, proceeds to the Golgi complex for synthesis, and is transported in a cytosol to the cell membrane. ANS: A The enzyme is transcribed from DNA by RNA in the nucleus, proceeds to the ribosome for synthesis, and is transported in a secretory vesicle to the cell membrane. The other options do not correctly describe this process. . PTS: 1 REF: Page 7 | Figure 1-5 6. During which phase of the cell cycle is DNA synthesized? a. G1 c. G2 b. S d. M ANS: B The four designated phases of the cell cycle are: (1) the G1 phase (G = gap), which is the period between the M phase (M = mitosis) and the start of DNA synthesis; (2) the S phase (S = synthesis), during which DNA is synthesized in the cell nucleus; (3) the G2 phase, during which RNA and protein synthesis occurs, the period between the completion of DNA synthesis and the next phase (M); and (4) the M phase, which includes nuclear and cytoplasmic division. PTS: 1 REF: Page 37 7. What organic compound facilitates transportation across cell membranes by acting as receptors, transport channels for electrolytes, and enzymes to drive active pumps? a. Lipids c. Proteins b. Proteases d. Carbohydrates ANS: C Proteins act as (1) recognition and binding units (receptors) for substances moving in and out of the cell; (2) pores or transport channels for various electrically charged particles called ions or electrolytes and specific carriers for amino acids and monosaccharides; and (3) specific enzymes that drive active pumps that promote the concentration of certain ions, particularly potassium (K+), within the cell while keeping concentrations of other ions, for example, sodium (Na+), below the concentrations found in the extracellular environment. The other options do not correctly describe this process. PTS: 1 REF: Page 13 | Page 15 8. Understanding the various steps of proteolytic cascades, such as caspase-mediated apoptosis and complement cascades, may be useful in designing drug therapy for which human diseases? a. Cardiac and vascular disorders b. Autoimmune and malignant disorders c. Gastrointestinal and renal disorders d. Endocrine and gastrointestinal disorders ANS: B Understanding the various steps involved in this process is crucial for designing drug interventions. Dysregulation of proteases features prominently in many human diseases, including cancer, autoimmunity, and neurodegenerative disorders. The other options do not correctly describe this process. PTS: 1 REF: Page 15 9. Which structure prevents water-soluble molecules from entering cells across the plasma membrane? a. Carbohydrate chains c. Membrane channel proteins b. Glycoprotein channels d. Lipid bilayer ANS: D The bilayer’s structure accounts for one of the essential functions of the plasma membrane. It is impermeable to most water-soluble molecules (molecules that dissolve in water) because the water-soluble molecules are insoluble in the oily core region. The bilayer serves as a barrier to the diffusion of water and hydrophilic substances while allowing lipid-soluble molecules, such as oxygen (O2) and carbon dioxide (CO2), to diffuse through it readily. The other options do not correctly describe this process. PTS: 1 REF: Pages 12-13 10. The fluid mosaic model explains: a. How a cell membrane functions b. Why our bodies appear to be solid c. How tissue is differentiated d. How fluid moves between the intracellular and extracellular compartments ANS: A The fluid mosaic model accounts for the flexibility of cellular membranes, their self-sealing properties, and their impermeability to many substances. The remaining options do not explain the mosaic model. PTS: 1 REF: Page 12 | What's New box 11. Which form of cell communication is used to communicate within the cell itself and with other cells in direct physical contact? a. Protein channel (gap junction) b. Plasma membrane–bound signaling molecules (involving receptors) c. Hormone secretion such as neurotransmitters d. Extracellular chemical messengers such as ligands ANS: A Cells communicate by using hundreds of kinds of signal molecules, for example, insulin. Cells communicate in three main ways; they display plasma membrane–bound signaling molecules (receptors) that affect the cell itself and other cells in direct physical contact. The other options do not correctly describe this process. PTS: 1 REF: Page 20 12. Which mode of chemical signaling uses blood to transport communication to cells some distance away?

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PATHOPHYSIOLOGY THE BIOLOGICAL 8TH EDITION MCCANCE
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PATHOPHYSIOLOGY 8TH EDITION MCCANCE HUETHER TEST BANK
m m m m m m




CHAPTER 1: CELLULAR BIOLOGY
M M M




MULTIPLE mCHOICE



1. Which mstatement mbest mdescribes mthe mcellular mfunction mof mmetabolic mabsorption?
a. Cells mcan mproduce mproteins. c. Cells mcan mtake min mand muse mnutrients.
b. Cells mcan msecrete mdigestive menzymes. d. m Cells mcan msynthesize mfats.

ANS: m C

In mmetabolic mabsorption, mall mcells mtake min mand muse mnutrients mand mother msubstances
mfrom mtheirm
surroundings. mThe mremaining moptions mare mnot minclusive min mtheir
mdescriptions mof mcellular mmetabolic mabsorption.




PTS: m m m 1 REF: m Page m2



2. Most mof ma mcell’s mgenetic minformation, mincluding mRNA mand mDNA, mis mcontained min mthe:
a. Mitochondria c. Nucleolus
b. Ribosome d. m m m Lysosome

ANS: m C

The mnucleus mcontains mthe mnucleolus, ma msmall mdense mstructure mcomposed mlargely mof
mRNA, mmost mof mthe mcellular mDNA, mand mthe mDNA-binding mproteins, msuch mas mthe


mhistones, mwhich mregulate mits mactivity. mThe mother moptions mdo mnot mcontain mmost mof ma


mcell’s mgenetic minformation.




PTS: m m m 1 REF: m Page m2



3. Which mcomponent mof mthe mcell mprodNuU
ceRsSIhNyGdTroBg.CenOM
peroxide m(H2O2) mby musing moxygen
mto mremove mhydrogen matoms mfrom mspecific msubstrates min man moxidative mreaction?
a. Lysosomes c. Ribosomes
b. Peroxisomes d. m Oxyhydrosomes

ANS: m B

Peroxisomes mare mso mnamed mbecause mthey musually mcontain menzymes mthat muse moxygen mto
mremove mhydrogen matoms mfrom mspecific msubstrates min man moxidative mreaction mthat



NURSINGTB.COM

,PATHOPHYSIOLOGY 8TH EDITION MCCANCE HUETHER TEST BANK
m m m m m m




mproduces mH2O2, mwhich mis ma mpowerful moxidant mand mpotentially mdestructive mif mit
maccumulates mor mescapes mfrom mperoxisomes. mRibosomes mare mRNA-protein mcomplexes


m(nucleoproteins) mthat mare msynthesized min mthe mnucleolus mand msecreted minto mthe


mcytoplasm mthrough mpores min mthe mnuclear menvelope mcalled mnuclear mpore mcomplexes.


m Lysosomes mare msaclike mstructures mthat moriginate mfrom mthe mGolgi mcomplex mand mcontain


mmore mthan m40 mdigestive menzymes mcalled mhydrolases, mwhich mcatalyze mbonds min mproteins,


mlipids, mnucleic macids, mand mcarbohydrates. mOxyhydrosomesm are minvolved min menzyme
mproduction.




PTS: m m m 1 REF: m Page m8



4. Which mcell mcomponent mis mcapable mof mcellular mautodigestion mwhen mit mis mreleased
m during mcellminjury?
a. Ribosome c. Smooth mendoplasmic mreticulum
b. Golgi mcomplex d. m Lysosomes

ANS: m D




NURSINGTB.COM

,PATHOPHYSIOLOGY 8TH EDITION MCCANCE HUETHER TEST BANK
m m m m m m




The mlysosomal mmembrane macts mas ma mprotective mshield mbetween mthe mpowerful mdigestive
menzymes mwithin mthe mlysosome mand mthe mcytoplasm, mpreventing mtheir mleakage minto mthe


mcytoplasmic mmatrix. mDisruption mof mthe mmembrane mby mvarious mtreatments mor mcellular


minjury mleads mto ma mrelease mof mthe mlysosomal menzymes, mwhich mcan mthen mreact mwith mtheir


mspecific msubstrates, mcausing mcellular mself-digestion. mThe mother moptions mdo mnot mcorrectly


mdescribe mthismprocess.



PTS: m m m 1 REF: m Pages m7-8



5. What mis mthe msequence mof msteps min mthe mdevelopment mof ma mdigestive menzyme mby mthe
m pancreasmcells mfrom mthe minitial mtranscription mto mthe mrelease mfrom mthe mcell?
a. The menzyme mis mtranscribed mfrom mDNA mby mRNA min mthe mnucleus, mproceeds
to mthemribosome mfor msynthesis, mand mis mtransported min ma msecretory mvesicle
m

mto mthe mcell mmembrane.

b. The menzyme mis mtranscribed mfrom mRNA mby mDNA min mthe mnucleus, mproceeds mto
mthe mlysosome mfor msynthesis, mand mis mtransported min man mencapsulated

mmembrane mto mthe mcellm membrane.
c. The menzyme mis mtranscribed mby mthe mmitochondria min mthe mnucleus, mproceeds mto
mthe mribosome mfor msynthesis, mand mis mtransported min ma mcytoskeleton mto mthe

mcell mmembrane.

d. The menzyme mis mtranscribed mfrom mDNA mby mRNA min mthe mnucleus, mproceeds mto
mthe mGolgi mcomplex mfor msynthesis, mand mis mtransported min ma mcytosol mto mthe mcell

mmembrane.



ANS: m A

The menzyme mis mtranscribed mfrom mDNA mby mRNA min mthe mnucleus, mproceeds mto mthe
mribosomem
for msynthesis, mand mis mtransported min ma msecretory mvesicle mto mthe mcell
mmembrane. mThe mother moptions mdo mnot mcorrectly m describe mthis mprocess.



NURSINGTB.COM

PTS: m m m 1 REF: m Page m7 m| mFigure m1-5



6. During mwhich mphase mof mthe mcell mcycle mis mDNA msynthesized?
a. G1 c. G2
b. S d. m M

ANS: m B

The mfour mdesignated mphases mof mthe mcell mcycle mare: m(1) mthe mG1 mphase m(G m= mgap), mwhich
mis mthe mperiod mbetween mthe mM mphase m(M m= mmitosis) mand mthe mstart mof mDNA msynthesis;


m(2) mthe mS mphasem(S m= msynthesis), mduring mwhich mDNA mis msynthesized min mthe mcell
mnucleus; m(3) mthe mG2 mphase, mduring mwhich mRNA mand mprotein msynthesis moccurs, mthe




NURSINGTB.COM

, PATHOPHYSIOLOGY 8TH EDITION MCCANCE HUETHER TEST BANK
m m m m m m




m period mbetween mthe mcompletion mof mDNA msynthesis mand mthe mnext mphase m(M); mand m(4)
m the mM mphase, mwhich mincludes mnuclear mand mcytoplasmic mdivision.



PTS: m m m 1 REF: m Page m37



7. What morganic mcompound mfacilitates mtransportation macross mcell mmembranes mby
macting masmreceptors, mtransport mchannels mfor melectrolytes, mand menzymes mto mdrive
mactive mpumps?

a. Lipids c. Proteins
b. Proteases d. m Carbohydrates

ANS: m C




NURSINGTB.COM

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