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379 Cards in this Set
- Front
- Back
Head of a phospholipid is
|
lipophobic = hydrophilic
|
|
Tail of a phospholipid is
|
hydrophobic = lipophilic
|
|
Function of glycocalyx?
|
short chain of carbohydrates that functions in cell-to-cell binding and
recognition. |
|
Proteins extending from the vesicle membrane _______, bind with plasma membrane proteins, the ______ (t for target), this causes the lipid layers of the vesicle and cell membrane to join together.
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Proteins extending from the vesicle membrane vSNAREs, bind with plasma membrane proteins, the tSNAREs (t for target), this causes the lipid layers of the vesicle and cell membrane to join together.
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In endocytosis, _________, found on the cytoplasmic side of the infolding is responsible for deforming the membrane.
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Clathrin protein
|
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In phagocytosis, parts of plasma membrane form _______ and flow around large molecules such as bacteria or cellular debris and engulf it.
By this way, a membranous vesicle, called a ______ is formed. |
-pseudopodes/pseudopodia
-phagosome |
|
main function of cells lining the small intestine, absorption
of the nutrients |
pinocytosis
|
|
Free ribosomes make the protein used ________.
Ribosomes attached on the surface of rER make the proteins used ____________ or ______________. |
-in the cytosol
-for cell membrane or exported out of the cell |
|
__________ is a ribosome-studded system of membrane-walled envelopes in cytosol, called ________.
|
-rough ER
-cisternae |
|
___________ produces steroids and lipids; ______ is the precursor to steroids
|
-smooth ER
-Cholesterol |
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___________ is a stack of 3-10 disc-shaped envelopes, or ________, which are bound by membrane
|
-golgi
-cisternae |
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Cisternae have a ______ and a _________ face
|
-cis (convex)
-trans (concave) |
|
__________ inner membrane is folded into projections called cristae
|
mitochondria
|
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_______ are spherical, membrane-walled sacs containing digestive enzymes called _________
|
-lysosomes
-Acid hydrolases |
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Lysosomes fuse with _________ and empty their enzymes into them.
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phagosomes
|
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___________ a fatal genetic lipid storage disorder in which harmful quantities of a fatty substance called ___________ build up in tissues and nerve cells in the brain.
|
-Tay-Sachs
-ganglioside GM2 |
|
In Tay-Sachs, __________
accumulate in the cell membrane specially on neurons, resulting in mental retardation, blindness, spastic movements and death within 1.5 years from birth. |
glycolipids
|
|
In ________ the lack of the ____________ enzyme causes harmful substances to build up in the liver, spleen, bones, and bone marrow. The substances prevent cells and organs from working properly.
|
-Gaucher's
-glucocerebrosidase |
|
Gaucher's type 1
|
involves bone disease, anemia, an enlarged spleen and thrombocytopenia; affects both children and adults.
|
|
Gaucher's type 2
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usually begins in infancy with severe neurologic involvement. This form can lead to rapid, early death
|
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Gaucher's type 3
|
disease may cause liver, spleen, and brain problems. Patients may live into adulthood.
|
|
Symptoms of gauchers
|
Bone pain and fractures
Enlarged spleen Enlarged liver Lung disease Seizures |
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_________ are membrane-walled, enzyme-containing sacs and contain oxidase and catalase enzymes.
________ use oxygen to neutralize aggressively reactive substances called free radicals, by converting them to hydrogen peroxide. |
-peroxisomes
-oxidases |
|
___________ are cylindrical structures made of ___________. They radiate out from the centrosome region close to the nucleus. They give the cell its shape and they organize the distribution and transport of various organelles within the cytoplasm
|
-microtubules
-tubulin protein |
|
________ are fine filaments of contractile protein called _______; they are labile
|
-microfilaments (actin filaments)
-actin |
|
_________ are tough insoluble and stable protein fibers which act to resist tension placed on the cell.
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intermediate filaments
|
|
________ is a spherical structure in the
cytoplasm near the nucleus. It consists of an outer cloud of protein called ______ and an inner pair of __________ |
-the centrosome
-matrix and an inner pair of centrioles |
|
Matrix protein is involved in?
|
the elongation of microtubules and mitotic spindle of microtubules radiates from it in dividing cells.
|
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Impermanent structures in the cytoplasm such as lipid droplets and glycogen containing glycosomes.
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Cytoplasmic inclusions
|
|
centrioles?
|
paired perpendicular cylindrical bodies composed of micotubules
|
|
________ are paired cylindrical bodies perpendicular to one another and each composed of _______ of microtubules
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-centrioles
-nine triplets |
|
______ make spindles
|
asters
|
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______ and _____ also contain microtubules
|
cilia and flagellum
|
|
_____________ has pores and
is continuous with endoplasmic reticulum |
nuclear envelope
|
|
dark staining body within the nucleus; contains parts of chromosomes and is
cell’s ribosome producing machine (has genes that code for rRNA |
nucleolus
|
|
_____is the granular thread-like
material in the nucleus composed of DNA (Deoxyribonucleic acid) and histone proteins |
chromatin
|
|
chromatin is
|
non dividing
|
|
DNA helix wraps around clusters of _______ spherical proteins called ______
|
-eight
-histones |
|
Each cluster of DNA and histones is called a _________.
|
nucleosome.
|
|
centrioles begin to replicate in?
they finish in? |
G1
G2 |
|
enzymes for cell division are synthesized in?
|
G2
|
|
In _______microtubule arrays called ________, extending from the centrosome.
|
-prophase
-asters |
|
the chromatids are held together by __________ and a protein complex called ________
|
-centromere
-cohesin |
|
spindles push the centrioles farther apart. spindles connected to the chromosome are called ______ and others are called ______
|
-kinetochores
-polar spindles |
|
_________, an enzyme which cleaves ________, start to separates the chromatids
|
-Separase
-cohesin |
|
Is anaphase short or long?
|
short
|
|
For a short period, the cell has 2 nuclei until it is completely separated by the process of ?
|
CYTOKINESIS
|
|
synapis? what is it and when?
|
pairing of 46 homologs at arms-end. occurs in Meiosis 1
|
|
crossing over occrus when?
|
meiosis 1
|
|
ploidy after meiosis 1?
meiosis 2? |
-haploid replicated
-haploid unreplicated |
|
does synapsis or crossing over occur in meiosis 2?
|
no b/c meiosis 2 is like mitosis
|
|
Ploidy of the following:
Down syndrome? Klinefelter? Turners? |
Down syndrome (trisomy 21)
Klinefelter syndrome (XXY) Turner syndrome (XO) is monosomy |
|
Diseases like turner's and Klinefelter occur because?
|
because of non-disjunction in meiosis 2
|
|
Klinefelter genotype and phenotype?
|
genotype is male
phenotype is female |
|
Monosomy signs and symptoms?
|
Turner's signs and symptoms:
Webbed neck Mental retardation Speech and learning problems Deafness |
|
What can restrict aging according to the mitochodrial theory?
|
-Vitamin C & E
-restriction of caloric intake |
|
Genetic theories of aging proposes that aging is programmed into our genes ; aka?
|
senescence
|
|
apoptotic bodies
|
membrane enclose cell framents after apoptosis
|
|
common features of apoptotic cells?
|
condensed chromatin, broken up nucleus and membrane
|
|
Certain ________, such as _________, may also activate _________ that degrade regulatory and structural proteins in the nucleus and cytoplasm, leading to the morphological changes characteristic of apoptosis.
|
-cytokines
-tumor necrosis factor (TNF) -caspases |
|
Too much apoptosis?
|
Alzheimer disease
|
|
too little?
|
cancer and other autoimmune diesease
|
|
difference between benign and malignant neoplasm
|
benign is encapsulated and slow growing
malignant isn't encapsulated and grows fast |
|
_________ or ________may lead to the formation of oncogenes.
|
Genetic accidents or viruses
|
|
Notable diseases caused by oncogenes?
|
Bladder cancer and acute myelogenous leukemia are caused by occogenes
|
|
Muscle is contractile tissue of the body and is derived from the ___________ of embryonic germ cells
|
mesodermal layer
|
|
Simple epithlelium = ?
Stratified = ? |
Simple epithlelium = one layer
Stratified = multiple layers |
|
There is only a single layer of cells, but the position of the nuclei gives the impression that it is stratified.
|
Pseudostratified with cilia/pseudostratified columnar epithelium
|
|
Location and Function of simple squamous
|
diffusion
located in alveoli, lining of body cavities, and capliaries |
|
Location and Function of simple cuboidal
|
secretion and absorption
glands and ducts, kidney tubules, surface of female ovaries and male testes |
|
simple cuboidal epithelium also constitute the ___________ which produces the egg cells in the female ovary and the sperm cells in the male testes.
|
-germinal epithelium
|
|
Location and Function of simple columnar - non-ciliated
|
secretion
lines most of digestive tract (stomach to rectum) |
|
Location and Function of simple columnar - ciliated
|
secretion
lines uterine tubes; bronchioles |
|
Location and Function of stratified squamous - non-keratin
|
protection
vagina |
|
Location and Function of stratified squamous - keratin
|
protection
epidermis of skin |
|
Location and function of stratified cuboidal
|
protection and secretion
large exocrine gland ducts (sweat glands and male urethra) |
|
Location and function of stratified columnar
|
protection and secretion
large exocrine gland ducts (salivary glands and male urethra) |
|
Location and function of pseudostratified columnar - non-ciliated
|
RARE
male epididymis; male vas deferins |
|
Location and function of pseudostratified columnar - ciliated
|
Secretion
Lines upper respiratory tract including nasal cavity, part of pharynx, larynx and bronchi |
|
Location and function of transitional epithelium
|
relaxtion and stretching to accommodate urine volume changes
lines urinary bladder, ureters, part of urethra |
|
most common form of secretion?
|
merocrine secretion
|
|
merocrine secretion
|
form membrane-bound secretory vesicles internal to the cell. These are moved to the apical surface where the vesicles coalesce with the membrane on the apical surface to release the product.
|
|
apocrine secretion
|
apical portions of cells are pinched off and lost during the secretory process. This results in a secretory product that contains a variety of molecular components including those of the membrane.
|
|
example of apoceine secretion
|
mammary glands
|
|
holocrine secretion
|
involves death of the cell. The secretory cell is released and as it breaks apart, the contents of the cell become the secretory product.
|
|
most complex secretory product?
examples? |
-holocrine
-sweat glands located in the axillae, pubic areas, and around the areoli of the breasts; Sebaceous glands also |
|
tight junctions are formed by _______ and ________ proteins
|
claudin and occludin
|
|
two disc like plaques connected across intracellular space
|
demosomes
|
|
In a desmosome, ______inserts into plague at cytoplasmic side; the palques are connected across intracelluar junction by ________
|
-keratin
-cadherins |
|
________ are passageways between two adjacent cells. They are made up ____ proteins called ______ to make a pore called _____
|
They are made up 6 proteins called connexins to make a pore called connexon
|
|
Basal lamina + reticular fibers =?
|
basement membrane
|
|
marfan syndrome
|
is an autosomal dominant genetic disorder of the connective tissue characterized by disproportionately long limbs, long thin fingers, a relatively tall stature, and a predisposition to cardiovascular abnormalities, specifically those affecting the heart valves and aorta
|
|
Marfan syndrome has been linked to a defect in the gene on ________ which encodes a ______ called ________.
|
-chromosome 15
-glycoprotein -fibrillin-1 |
|
__________ syndrome is a group of rare genetic disorders affecting humans and domestic animals caused by a defect in ________ synthesis .
|
-Ehlers-Danlos
-Collagen I and III |
|
Most common location of gauchers
|
bone marrow
|
|
About 20% of the extracellular fluid is contained the _________________, where it comprises the fluid portion of the blood aka _________.
|
-vessels of cardiovascular system
-plasma |
|
fluids, as interstitial, or tissue, fluid, within a matrix of glycoproteins and proteoglycans
|
extracellular matrix
|
|
extracellular matrix consists of the protein fibers ______ and ________
|
-collagen
-elastin |
|
Intergrins
|
are a class of glycoproteins that extend from the cytoskeleton within a cell, through its plasma membrane, and into the exracellular matrix. By binding to components within the matrix, they serve as adhesion molecule between cells and the extracellular matrix
|
|
Does permeability increase with concentration difference?
oil/water partition coefficient? |
-no it decreses
-yes |
|
Example of competition in carrier-mediate transport?
|
galactose is a competitive inhibitor of glucose transport in the small intestine.
|
|
Insulin binds to target cell receptor -> activates ______, which then _________
|
activates GLUT4 which inserts into the membrane and allows glucose to enter
|
|
Specific inhibitors of Na+, K+-atpase are ?
|
the cardiac glycoside drugs ouabain and digitals.
|
|
Ca2+ ATPase in most cells?
Ca2+ ATPase in SR of muscle cells cells? |
-Pumps calcium to ECF
-pumps calcium to the lumen of the SR or ER |
|
H+/K+ ATPase location/function?
Inhibited by? |
-in gastric parietal cells transports H+ into lumen of the stomach against its electrochemical gradient.
-It is inhibited by omeprazole. |
|
examples of cotransport
|
Na+-glucose cotransport in the small intestine and Na+-K+-2Cl- cotransport in the renal thick ascending limb.
|
|
example of countertransport
|
Na+-Ca2+ exchange
|
|
colligative property can be measured by freezing point depression
|
Osmolarity
|
|
The higher the osmotic pressure of a solution ?
|
the greater the water flow into it.
|
|
oncotic pressure
|
is the osmotic pressure created by proteins (plasma proteins).
|
|
Reflection coefficient (RC)
|
is a number between zero and one that describes the ease with which a solute permeates a membrane.
|
|
If the RC is one
|
the solute is *impermeable*. Therefore, it is retained in the original solution, it creates an osmotic pressure, and it causes water flow. Serum albumin (a large solute) has a reflection coefficient of nearly one.
|
|
If RC is zero
|
the solute is *completely permeable*. Therefore, it will not exert any osmotic effect, and it will not cause water flow. Urea (a small solute) has a reflection coefficient of close to zero and it is, therefore, an ineffective osmole.
|
|
If the reflection coefficient is one, the solute will exert _______ effective osmotic pressure. If the reflection coefficient is zero, the solute will exert _______ effective osmotic pressure.
|
-maximal
-no |
|
genetic defect in CF involves
|
a particular glycoprotein that forms chloride (Cl-) channels in the apical membrane of the epithelial cells. This protein known as CFTR ( for cystic fibrosis transmembrane conductance regulator)
|
|
CF mechanism
|
CTFR gene is mutated or alterated -> CFTR cannot control excess production of chloride -> patient has excess excretion of Cl into lumen of different organs -> sodium follows Cl -> osmotic pressure increases in the lumen and causes reabsorption of fluid and excretion of fluid into lumen -> leads to local inflammation and accumulation of neutrophils and other WBCs and formation of mucus inside the lumen -> causes obstruction of the lumen -> if occurs in the respiratory system the pt will have respiratory disorder -> if it occurs in the lumen of spermaticor the patient will have infertility -> if it occurs in the pancreatic lumen and causes pancreatitis -> if it occurs in the small or large intestine it causes diarrhea
|
|
_______ and primarily ________ transmit change in osmolarity to CNS
|
Glosopharyngeal nerve (cranial 9)
Vegus nerve (cranial 10) |
|
central osmoreceptor is located in the ______. The two nuclei are ____ and _____.
|
-hypothalamus
-supraotic -paraventricular |
|
two hypothalamic nuclei secrete ADH which has receptors on
|
collecting tubule of nephron
|
|
ADH binds to receptor and causes stimulation of the _______, which reabsorbs water from the urine into the blood stream -> ADH corrects dehydration via reabsorption of fluid and decreases osmotic pressure and dilutes concentrated blood.
|
peritubullar capillary
|
|
_______ may occur, for example, when a damaged _______ as in ________ is unable to produce sufficient amounts of ________, the major protein in the blood plasma
|
-edema
-liver as in cirrhosis -albumin |
|
Ligand-gated channels
|
open or closed by hormones, second messengers, or neurotransmitters.
|
|
equilibrium potential of Na
|
+65mV
|
|
equilibrium potential of Ca
|
+120mV
|
|
equilibrium potential of K
|
-85mV
|
|
equilibrium potential of Cl
|
-85mV
|
|
Inward current is ?.
Inward current ________ the membrane potential. |
Inward current is the flow of positive charge into the cells. Inward current depolarizes the membrane potential.
|
|
Outward current ________ the membrane potential.
|
hyperpolarizes
|
|
Action potentials have
|
stereotypical size and shape, are propagating, and are all-or-none
|
|
_________ blocks action potentials in nerves by binding to the voltage-gated, fast sodium channels in nerve cell membranes, essentially preventing any affected nerve cells from firing by blocking the channels used in the process.
|
Tetrodotoxin
|
|
Inhibitory neurotransmitters ________ the postsynaptic membrane; excitatory neurotransmitters _________ the postsynaptic membrane.
|
-hyperpolarize
-depolarize |
|
___________ catalyzes the formation of Ach from acetyl coenzyme A (CaA) and choline in the presynaptic terminal.
|
Choline acetyltransferase
|
|
Ach is stored in synaptic vesicles with _____ and ______ for later release.
|
ATP and proteoglycan
|
|
One-half of the choline is taken back into the presynaptic ending by ___________ and used to synthesize new Ach
|
Na+-choline cotransport
|
|
Ach inhibitors- ________ and ________ blocks choline reuptake and depletes the presynaptic endings of Ach stores.
|
neostigmine, and Hemicholinium
|
|
myasthenia gravis
|
-caused by presence of antibodies to the Ach receptors.-characterized by skeletal muscle weakness and fatigability resulting from a reduced number of Ach receptors on the muscle end plate.
-The size of the EPP is reduced; therefore, it is more difficult to depolarize the muscle membrane to threshold and to produce action potentials.-Treatment : AChE inhibitors (neostigmine) |
|
inhibitory neurotransmitters?
|
gama-aminobutyric acid (GABA) and glycine.
|
|
dopamine produced by basal ganglia of brain (limbec system) controls pleasure feelings. What increases dopamine in this area of the brain?
|
– cocaine increases dopamine in this part of the brain
|
|
dopamine produced by hypothalamus has endocrine effect – what is it?
|
decreases prolactin excretion (prolactin produces milk in females during breast feeding; small amount of prolactin is in males and important for sexual behior – like kindness)
|
|
dopamine deficiency in _____ causes problem solving disorders?
|
frontal lobe (ADD)
|
|
dopamine deficiency in _____ causes parkinsons
|
brain stem
|
|
tumor causes excess prolactin - what can treat it?
|
dopamine
|
|
increased prolactin has what effect on sex hormones?
|
decreases them
females can't get pregnant males act like girls |
|
excess dopamine can cause
|
schizophrenia
|
|
norepi is removed from the synapse by reuptake or is metabolized in the presynaptic terminal by __________ and ___________
|
-monoamine oxide (MAO)
-catechol-O-methyltransferase (COMT) |
|
Metabolites of norepi breakdown?
|
a. 3,4-Dihydroxymandelic acid (DOMA
b. Normetanephrine (NMN) 3-Methoxy-4-hydroxyphenylglycol (MOPEG) 3-Methoxy-4 hydroxymandelic acid, or vanillylmandelic acid (VMA) |
|
In __________, urinary excretion of VMA is increased.
|
In pheochromocytoma, urinary excretion of VMA is increased.
|
|
Epinephrine is synthesized from norepinephrine by the action of _____________
|
phenylethanolamine-N-methyltransferase.
|
|
dopamine is metabolized by
|
COMT and MAO
|
|
D1 receptors ______ adenylate cyclase via a _________.
D2 receptors ______ adenylate cyclase via a _________. |
- D1 active via Gs protein
-D2 inhibit via Gi protein |
|
-Parkinson’s disease involves _______ of dopaminergic neurons that use the ______ receptors.
-Schizophrenia involves _______ levels of ______ receptors. |
-degradation of D2
-increased levels of D2 receptors |
|
-is present in high concentrations in the brain stem.
-is formed tryptophan. -is converted to melatonin in the pineal gland. |
serotonin
|
|
-is formed from histidine.
-is present in the neurons of the hypothalamus. |
histamine
|
|
-is the most prevalent excitatory neurotransmitter in the brain.
-has a kainate receptor, which is an ion channel for Na+ and K+. |
glutamate
|
|
inhibitory neurotransmitter with two types of receptors?
|
GABA
|
|
GABA-a receptor function?
What drugs work here? |
The GABAa receptor increases Cl- conductance and is the site of action of benzodiazepines and barbiturates.
|
|
GABA-b receptor function?
|
The GABAb receptor increases K+ conductance.
|
|
-is an inhibitory neurotransmitter found primarily in the spinal cord and brain stem.
-increases Cl- conductance. |
glycine
|
|
water accounts for ________of total weight for an adult
|
65-75%
|
|
properties of acids
|
-taste sour
-react strongly with metals (Zn + HCl) -are dangerous and can burn your skin |
|
properties of bases
|
-taste bitter
-feel slippery -are very dangerous and can burn your skin |
|
plasma buffer?
|
bicarb/carbonic acid
|
|
________ is an inherited autosomal recessive trait that affects the way the sugar is broken down, due to the lack of the enzyme __________
|
-galactosemia
-galactose-1-phosphate uridyl transferase. |
|
signs and symptoms of galactosemia?
|
-swollen and inflamed liver -kidney failure
-ovarian failure in girls -mental growth retardation-cataracts in the eyes |
|
treatment of galactosemia?
|
diet
|
|
Many drug molecules are partially bound to _________ in the plasma.
|
serum albumins
|
|
if protein and caloric intake are both inadequate, a condition known as ________ occurs; presents with a stoppage of growth, extreme muscle loss, and weakness
|
-marasmus
|
|
marasmus is characterised by energy deficiency aka
|
Cachexia.
|
|
___________ are the most important factor that can increase a person's cholesterol level
|
saturated fatty acids
|
|
What are the ketone bodies called?
|
acetoacetate
acetone B-hydroxybutryate |
|
________ is not technically a ketone but a carboxylic acid
|
beta-hydroxybutyrate
|
|
h BGL can cause nausea and vomiting bc the excess glucose irritates?
|
the vomiting center in the medula oblongata
|
|
ketosis?
ketoacidosis? |
ketosis - excess ketone bodies; not always harmful; no harmful change in pH
ketoacidosis - harmful; lowers pH to bad level |
|
ketone bodies are the by-product of?
|
muscle & fat breakdown
|
|
When ketone is excreted, ______is excreted along with it.
|
sodium
|
|
Symptoms of glucose and ketone-body overload that you didn't know?
|
pupil dilation
|
|
what ketone body is excreted through the lung and causes fruity smell?
|
acetone
|
|
any member of a group of lipid compounds that are derived enzymatically from fatty acids and have important functions in the animal body; are found in virtually all tissues and organs.
|
prostaglandins
|
|
role of prostaglandins
|
-cause constriction or dilatation in vascular smooth muscle cells -sensitize spinal neurons to pain -constrict smooth muscle -regulate inflammatory mediation -regulate calcium movement -regulate hormone regulation -control cell growth
|
|
what irritates females abd cavity during mensturation?
|
prostaglandins
|
|
___________ can be inorganic (e.g., metal ions such as Ca+, Mg2+).
|
Cofactors
|
|
________ are organic molecules, derived from water soluble vitamins such as niacin and riboflavin, that are needed for the function of particular enzymes
|
Coenzymes
|
|
coenzmes participate in enzyme-catalyzed reactions by transporting _________ and _______ from one enzyme to another.
|
-hydrogen atoms
-small molecules |
|
A pair of Hydrogen atoms in each pyruvate from glucose is used to
|
reduce NAD to NADH
|
|
glycolysis general reaction?
|
Glucose + 2NAD + 2 ADP + 2Pi
= 2pyruvic acid + 2 NADH + 2ATP |
|
Lactic acid/fermentation purpose
|
NADH reduces pyruvate to another molecule and goes back to NAD+ to form glycolysis again b/c the ETC isn't available w/o oxygen
|
|
The addition of two hydrogen atoms to pyruvic acid produces ?
|
lactic acid.
|
|
glycogenesis
|
formations of glycogen from glucose using an ATP
glucose -> glucose-6-phosphate -> glucose-1-phosphate -> glycogen |
|
the enzyme _______ removes the phosphate groups from glucose-1-phosphate as it polymerizes glucose to form glycogen.
|
glycogen synthase
|
|
The conversion of ______ to _________ is called glycogenolysis
|
-glycogen
-glucose 6-phosphate |
|
In glycogenolysis the enzyme _______ catalyzes the breakdown of glycogen to glucose1-phosphate
|
-glycogen phosphorylase
|
|
Only in ________, can the glucose 6-phosphate also be used to produce free glucose for secretion into the blood.
|
-the liver
-most tissues use glucose-6-phosphate |
|
What enzyme does the liver have that allows it to create glucose for secretion
|
glucose-6-phosphatase
|
|
two hormones that control glycogenolysis?
they stimulate? |
-glucagon & epi
-stimulate glycogen phosphorylase and inhibit glycogen synthetase |
|
gluconeogenesis
|
conversion of noncarbohydrate molecules (not just lactic acid but also amino acids and glycerol) through pyruvic acid to glucose
|
|
Enzyme in liver that converts lactic acid to pyruvic acid?
|
lactic acid dehydrogenase (LDH)
|
|
Two-way traffic between skeletal muscles and the liver is called ______.
|
The cori cycle
|
|
complexes I, II, III, and IV, plus two individual molecules, coenzyme Q and cytochrome c
|
the electron transport chain
|
|
ETC makes ____ATP?
Total aerobic respiration makes? |
32 ATP
36 ATP |
|
ETC occurs at?
|
the inner membraine
protons flow from intermembrane space thru the ATP synthase to the matrix |
|
In a process known as ________ enzymes remove two-carbon acetic acid molecules from the acid end of a fatty acid chain.
|
B-oxidation
|
|
The efferent fibers have their cell bodies in the ________, and they reach the sympathetic ganglia on both sides of the ________.
|
- spinal cord
-vertebral column |
|
The parasympathetic efferents reach their ganglia ____________
|
at or near the organs
|
|
sympathetic effect on sphincter?
|
closes them
|
|
sympathetic effect on glands, sphincter, and bladder
|
increased
glandular activity, sphincters open, bladder wall is relaxed (detrusor muscle) |
|
Preganglionic fibers synapse directly on ________ in the adrenal medulla.
|
chromaffin cells
|
|
-The chromaffin cells secrete _________(80%) and _______ (20%) into the circulation.
|
epinephrine (80%)
norepinephrine (20%) |
|
___________ is a tumor of the adrenal medulla that secretes excessive amounts of catecholamines and with increased excretion of __________
|
-Pheochromocytoma
-3-methoxy-4-hydroxymandelic acid (VMA). |
|
In the abd cavity some preganglionic fibers should pass through sympathetic chain without having synapse and should have synapse with ___________
|
paraverterbral ganglia (celiac, superior mesenteric, and inferior mesenteric) that supply the GI nervous system
|
|
efferent sympathetic cell bodies are in the ________ of the spinal chord
|
lateral horn
|
|
Peptidergic neurons in the parasympathetic nervous system release peptides such as _________ and __________
|
vasoactive inhibitory peptide and substance P
|
|
alpha 1 receptor locations?
|
vascular smooth muscle of the skin and splanchnic regions, the gastrointestinal (GI) and bladder sphincters, and the radial muscle of the iris.
|
|
alpha 1 receptor produces
|
-produce excitation (contraction ,constriction).
|
|
Alpha 1 receptors are equally sensitive to norepi and epi but only _________ is high enough in concentration to stimulate
|
norepi
|
|
mechanism of Alpha 1 receptors
|
G protein alpha stimulator, Phospholipase C, formation of inositol 1,4,5-triphospate (IP3) and increase in intracellular (Ca+).
|
|
Alpha 2 receptors are located in
|
presynaptic nerve terminals, platelets. Fat cells, and the walls of the GI tract.
|
|
result of alpha 2 stimulation?
|
-often produce inhibition (relaxation or dilation).
|
|
Alpha 2 mechanism
|
G protein alpha inhibitor, inhibition of adenylate cyclase and decrease in cyclic adenosine monophosphate (CAMP).
|
|
Beta 1 receptors are located in ?
|
the sinoatrial (SA) node, atrioventricular (AV) node, and ventricular muscle of the heart.
|
|
Beta 1 produces?
|
-produce excitation (increased heart rate, increased conduction velocity, increased contractility).
|
|
B1 receptors are sensitive to both norepinephrine and epinephrine, and are more sensitive than_________receptors.
|
-are sensitive to both norepinephrine and epinephrine, and are more sensitive than alpha1 receptors.
|
|
Beta 1 Mechanism of action:
|
activation G protein alpha stimulator, activation of adenylate cyclase and increase in cAMP.
|
|
Beta 2 receptors are located on
|
vascular smooth muscle of skeletal muscle, bronchial smooth muscle, and in the walls of the GI tract and bladder.
|
|
Beta 2 receptors produce
|
-produce relaxation (dilation of vascular smooth muscle, dilation of bronchioles, relaxation of the bladder wall.)
|
|
Beta 2 receptors are more sensitive to ________ than _______
|
epinephrine than to norepinephrine.
|
|
Beta 2 receptors are more sensitive to epinephrine than the ______
|
alpha 1 receptors.
|
|
Beta 2 Mechanism of action:
|
activation G protein alpha stimulator, activation of adenylate cyclase and increase in cAMP.
|
|
Location of nicotinic receptors
|
autonomic ganglia of the sympathetic and parasympathetic nervous systems, at the neuromuscular junction, and in the adrenal medulla. The receptors at these are similar, but not identical
|
|
stimulation of nicotinic receptors
|
produce excitation
|
|
Mechanism of action for nicotinic receptors?
|
Ach binds to alpha subunits of the nicotinic Ach receptor, The nicotinic Ach receptors are also ion channels for Na+ and K+
|
|
Location of muscarinic receptors?
|
heart, smooth muscle, and glands.
|
|
function of muscarinic receptors?
|
parasympathetic = rest and digest
|
|
relaxing mechanism of muscarinic?
|
Heart SA node: inhibition of adenylate cyclase, which leads to opening of K+ channels, slowing of the rate of spontaneous Phase 4 depolarization, and decreased heart rate
|
|
excitatory mechanism of muscarinic?
|
Smooth muscle and glands: formation of IP3 and increase in intracellular (Ca2+).
|
|
Medulla contains what autonomic centers
|
-Vasomotor center
-Respiratory center -Swallowing, coughing, and vomiting center |
|
Pons contains what autonomic centers
|
Pneumotaxic center
|
|
Midbrain contains what autonomic centers
|
-Micturition center
|
|
Hypothalamus contains what autonomic centers
|
-Temperature regulation center
-Thirst and food intake regulatory centers |
|
mostly presynaptic
|
A2
|
|
Stimulates insulin release
|
B2
|
|
mechanism of muscarinic receptors
|
Mechanism of action: increased intracellular calcium
|
|
mechanism of nicotinic receptors
|
Produce excitation (opening of Na-K channels, depolarization)
|
|
What receptor inhibits insulin secretion?
|
alpha
|
|
what receptor stimulates insulin excretion?
|
beta
|
|
Fastest fiber type?
Slowest fiber type? |
A-alpha is fastest
C is slowest |
|
Fiber of intrafusal fibers?
|
A-gamma
|
|
respond repetitively to a prolonged stimulus
|
Slowly adapting, or tonic, receptors
|
|
show a decline in action potential frequency with time in response to a constant stimulus.
|
Rapidly adapting, or phasic, receptors
|
|
examples of Rapidly adapting, or phasic, receptors
|
pacinian corpucle, light touch
|
|
examples of Slowly adapting, or tonic, receptors
|
muscle spindle, pressure, slow pain
|
|
Cell bodies of the primary afferent neurons are in _______ or ________
|
dorsal root or spinal cord ganglia.
|
|
second order neruon location?
special feature? |
located in brain or spinal cord
usually cross midline |
|
third order neuron location?
|
relay nuclei of thalamus
|
|
Fourth order neuron location?
|
appropriate area of cortext
|
|
dorsal column system
|
processes sensations of fine touch, pressure, two-point discrimination, vibration
|
|
second order neurons of the dorsal column system have no synapse in the _______ cross the midline in the _______
|
-spinal chord
-brain stem medulla |
|
anterolateral
|
-processes sensations of temperature, pain, and light touch.
|
|
second order neurons of the anterolateral column system cross the midline in the _______ and have no synapse in the _______
|
spinal chord
brainstem |
|
Neurotransmitters for nociceptors include ________. Inhibition of the release of it is the basis of pain relief by ______.
|
-substance P
-opioids |
|
Fast pain is carried by group ________ fibers. It has a rapid onset and offset, and is localized.
|
A-delta fibers
|
|
Slow pain is carried by _______. It is characterized as aching, burning, or throbbing that is poorly localized.
|
C fibers
|
|
carries taste sensations from the anterior two thirds of the tongue and soft palate
|
Cranial nerve VII, the facial nerve
|
|
carries taste sensations from the posterior one third of the tongue.
|
Cranial nerve IX the glossopharyngeal nerve
|
|
a branch of _______ carries some taste sensations from the back of the oral cavity (i.e. pharynx and epiglottis).
|
the vagus nerve
|
|
Salt taste receptor is stimulated by
|
Na influx followed by the opening of calcium channels
|
|
sour taste resceptor is from
|
H+ ions
|
|
bitter taste receptors act thru G protiens that release
|
gustducin
|
|
ageusia is associated with what condition?
|
Bell's palsy
|
|
What can cause Bell's palsy
|
neruological disorder/damage to nerve or herpes zoster virus
|
|
A condition characterized by a burning sensation on the tongue
|
glossodynia
|
|
The axons of the olfactory nerves are _______ fibers and are among the smallest and slowest in the nervous system
|
unmyelinated C
|
|
Cranial nerve ____, aka ______ carries info from olfactory receptor to olfactory bulb
|
CN 1, olfactory
|
|
Olfactory epithelium is also innervated by cranial _________ (trigeminal), which detects noxious or painful stimuli, such as ammonia
|
cranial nerve 5 (trigeminal)
|
|
fractures of the cribiform plate affect _______ and not ______
so you can still smell what? |
-cranial nerve 1 and not cranial nerve 5
-ammonia |
|
olfactory mechanism
|
G-olf protien activates adenylate cyclase which increases cAMP which opens Na channels
|
|
tough white fibrous layer that maintains, protects and supports the shape of the eye
|
sclera
|
|
The front of the sclera is transparent and is called the ______
|
cornea.
|
|
middle thin layer of the eye; vascular layer of the eye
|
choroid
|
|
ciliary body secretes small amounts of fluid that enter the posterior chamber and then the anterior chamber, the fluid should pass thru the _________and be drained into venous system.
|
canal of shlem
|
|
If there is a congenital problem that causes obstruction of canal of schlem or obstruction due to infection/tumor then ?
|
fluid can’t be released into venous system and causes glaucoma which increases the intraocular pressure from the excess accumulation of fluid in the eye; can cause blindness by damaging the retina and the optic nerve near the retina.
|
|
blind spot of retina?
|
optic disk, no receptors, where optic nerve leaves
|
|
The cornea and the lens of the eye focuses the light onto a small area of the retina called the __________ where the cone cells are densely packed
|
fovea centralis
|
|
How many rods are in the fovea?
|
none
|
|
__________cells form the optic nerve
|
Axons of ganglion cells
|
|
rhodopsin = ____ and _____
|
scotopsin
and retinal (vitamin A aldehyde) |
|
Light converts ______ to ______
|
11-cis-retinal to all-trans-retinal
|
|
What causes night blindness
|
Vitamin A deficiency
|
|
all-trans retinal goes thru a series of intermediates to form
|
meta-rhodopsin 2
|
|
metarhodopsin 2 activates_____ which activates ______
|
G protein alpha (transducin) which actives phosphodiesterase (PDE)
|
|
PDE decreases
|
cGMP
|
|
If the neurotransmitter is exitatory, then the response of the bipolar or horizontal cell to light is .
|
hyperpolarization (counter intuitive)
|
|
If the neurotransmitter is inhibitory, then the response of the bipolar or horizontal cell to light is .
|
depolarization (counter intuitive)
|
|
The most common cause of nyctalopia is ___________,
|
retinitis pigmentosa
|
|
retinitis pigmentosa?
|
a disorder in which the rod cells in the retina gradually lose their ability to respond to the light
|
|
_________ is the inability of the brain to make sense of or make use of some part of otherwise normal visual stimulus, and is typified by the inability to recognize familiar objects or faces
|
Visual agnosia
|
|
normal. Light focuses on the retina
|
Emmetropia
|
|
Hypertropia-
corrected with what lens? |
farsighted. light focuses behind the retina and is corrected with a convex lens.
|
|
Myopia-
corrected with what lens? |
nearsighted. Light focuses in front of the retina and is corrected with a biconcave lens.
|
|
Astigmatism.
corrected with what lens? |
Curvature of the lens is not uniform and is corrected with a cylindric lens.
|
|
The _______ is the smallest named bone in the human body. The stapes transfers the vibrations of the _______to the _________, a portion of the inner ear to which it is connected
|
-stapes
-incus to the oval window |
|
The _________ and ______ contain perilymph, which has a high _____ concentration.
|
-scala vestibuli and scala tympani
-Na+ |
|
The ________ contains endolymph, which has a high _____
|
-scala media
-K+ |
|
The spiral ganglion contains the cell bodies of the ________ nerve aka _______ which synapse on the hair cells.
|
auditory nerve aka CN VIII
|
|
The base of the basilar membrane (near the oval and round windows) is narrow and stiff. It responds best to ______frequencies.
|
high
|
|
The apex of the basilar membrane (near the helicotrema) is wide and compliant. It responds best to _____ frequencies.
|
low
|
|
Temporal lobe of brain; superior temporal gyrus area for T1 and T2
|
flip and read back again
|
|
_______ and ________ are the most common bacterial causes of otitis media
|
-Streptococcus pneumoniae and Haemophilus influenzae
-the common cold |
|
The ________ detect angular acceleration or rotation
|
semicircular canals
|
|
The ______ and _______ detect linear acceleration
|
utricle and saccule
|
|
The receptors are hair cells located at the end of each semicircular canal. Cilia on the hair cells are embedded in a gelatinous structure called the __________
|
cupula
|
|
If the stereocilia are bent toward the kinocilium, the hair cell _________. If the stereocilia are bent away from the kinocilium, the hair cell ________.
|
-depolarizes (excitation)
-hyperpolarizes (inhibition) |
|
cell body of the neuron and dendrites contain ________ but the axon does not
|
Nissl bodies (rER)
|
|
Form a single layer of cuboidal cells lining the
central cavities of the brain and spinal cord. They have microvilli also |
ependyma
|
|
proliferation of __________ during damage prevents regeneration of axons on CNS
|
astrocytes
|
|
________ is hyperplasia and hypertrophy of astrocytes that occur in reaction to CNS injury.
|
Gliosis
|
|
Astrocytomas and glioblastomas are tumors of
|
astrocytes
|
|
multiple sclerosis
|
occurs between ages of 20-40 year, demyelination in CNS, usually starts with optic nerve, spinal cord and cerebellum. Axonal degeneration as a result of demyelination and/or early in the course of the disease is part of the disability.
|
|
Schwan cells form mylen over how many cells? oligs over how many?
|
Shwann = 1
oligs = many |
|
white matter is from? deeper or outter?
|
from axons and is deeper in brain
|
|
grey matter is from? deeper or outer?
|
from cell bodies/dendrites and is outer
|
|
important in the embryonic development of sensory neurons and sympathetic ganglia
|
Neurotrophin-3
|
|
The composition of CSF is approximately the same as that of the ________ of the brain, but differs significantly from blood.
|
interstitial fluid
|
|
CSF and Blood have similar concentrations for?
|
Na+
Cl- HCO3- Osmolarity |
|
CSF has less of what components than the blood has?
|
K+
Ca2+ Glucose Cholestrol* Protein* |
|
CSF has more of what components than the blood has?
|
Mg2+
Creatinine |
|
CSF has none of what?
|
Cholestrol*
Protein* |
|
chemical synapses have what directionality?
Electrical? |
-chemical = unidirectional
-electrical = bidirectional |
|
dopamine is found in high concentration at
|
the basal ganglia and hypothalamus
|
|
norepi is found in the CNS at
|
the hypothalamus
|
|
Glycine is found principally in
|
synapses in the spinal cord
|
|
Glutamate?
|
is an excitatory amino acid neurotransmitter in many central nervous neurons.
|
|
Electrical synapses are _______ junctions, which are made of the monomer _________ to form one ________
|
-gap junctions
-connexin -connexon |
|
what drug block Dopamine receptors postsynaptically
|
Phenothiazines
schizophrenia |
|
what type of nerves are easier to block?
|
-bigger nerves
|
|
General anesthetics block _______
Local anesthetics block ______ |
-General anesthetics block synaptic transmission.
-Local anesthetics block nerve conduction |
|
If neurons of the brainstem that make serotonin—serotonergic neurons—are abnormal, there is a risk of
|
SIDS
|
|
does oral serotonin enter sertogenic pathways?
|
no it doesn't pass the BBB
|
|
dopamine deficiency in what area of the brain can cause a behavioral disorder? what disorder is an example?
|
-prefrontal cortext
-ADD |
|
The neurotransmitter most often associated with EPSPs is the amino acid _______, and is the main excitatory neurotransmitter in the central nervous system.
|
glutamate
|
|
The most common inhibitory neurotransmitters in the nervous system are ______ and ______.
mechanism of inhibition? |
-GABA and glycine
-open Cl channels |
|
________ forms part of the "lipostat" system along with leptin and corticotropin-releasing hormone (CRH).
|
neuropeptide Y
|
|
NPY has been associated with a number of physiologic processes in the brain, including
|
the regulation of energy balance, memory and learning, and epilepsy
|
|
leptin is produced by _______ and crontrols the release of ________
|
-adipose tissue
-release of corticotropin releasing hormone and appetite |
|
endothelium-derived relaxing factor is biosynthesized from arginine and oxygen
|
NO
|
|
function of NO
|
blood vessel dilatation, neurotransmission, modulation of the hair cycle, and penile erections
|
|
special feature of NO in high altitude populations?
|
increased NO helps avoid hypoxia
|
|
Origin on bone is at _______ movable attachment
Insertion is on _____ movable attachment |
-less
-more |
|
Muscle cell Plasma membrane is called a __________
Muscle cell Cytoplasm is called _______ |
-sarcolemma
-sarcoplasm |
|
A myofibril is a long row of repeating segments called ________
|
sarcomeres
|
|
Z disc (Z line)
|
boundaries of each sarcomere
|
|
Thin (actin) filaments
|
extend from Z disc toward the center of the sarcomere
|
|
Thick (myosin) filaments
contain what type of enzymes? |
located in the center of the sarcomere
Overlap inner ends of the thin filaments contain ATPase enzymes |
|
A bands
|
full length of the thick filament, includes inner end of thin filaments
|
|
H zone
|
center part of A band where no thin filaments occur
|
|
M line
|
in center of H zone, contains tiny rods that hold thick filaments together
|
|
I band
|
region with only thin filaments, lies within two adjacent sarcomeres
|
|
Impulses in muscle contraction are further conducted by________, which are deep invaginations of the sarcolemma
|
t tubules
|
|
Tn C (troponin C)
|
binds to calcium, initiates muscle contraction
|
|
Tn T (troponin T)
|
binds troponin complex to tropomyosin
|
|
Tn I (troponin inhibitor)
|
inhibits actin binding to myosin heads in resting muscle
|
|
group IIb afferents that detect tension?
|
golgi tendon organ
|
|
group II afferents that are distributed throughout muscle. They detect vibration.
|
Pacinian corpuscles
|
|
group III and IV afferents) detect noxious stimuli.
|
Free nerve endings
|
|
-make up the bulk of muscle.
-are innervated by alpha-motoneurons. -provide the force for muscle contraction. |
extrafusal fibers
|
|
-are smaller than extrafusal muscle fibers.
-are innervated by gamma-motoneurons. -are encapsulated in sheaths to form muscle spindles. -run in parallel with extrafusal fibers. But not for entire length of the muscle. |
intrafusal fibers
|
|
extrafusal fibers are innervated by __________ motorneurons
intrafusal fibers are innervated by __________ motorneruons |
alpha
gamma |
|
Function of gamma-motoneurons
|
-innervate intrafusal muscle fibers.
-adjust the sensitivity of the muscle spindle so that it will respond appropriately during muscle contraction. |
|
Stimulation of group Ia afferents stimulates __________ in the spinal cord. This stimulation in turn causes contraction and shortening of the muscle. Thus, the original stretch is opposed muscle length is maintained.
|
-alpha-motoneurons
|
|
In smooth muscle .Ca++ combines with a protein _________
|
calmodulin
|
|
the calmodulin-Ca++ combines with and activates _____________, then it binds to _______
|
myosin light-chain kinase
actin |
|
myosin light-chain kinase is ?
|
an enzyme that catalyzes the phosphorylation of myosin light chains
|
|
Troponin c is activated by ________ and ________ in smooth muscle
|
calcium and calmodulin
|
|
HTN can be caused by excess Ca++ which constricts blood vessels. treatment?
|
calcium channel blockers
|
|
The affected muscles enlarge with fat and connective tissue but the muscle fibers actually degenerate
|
muscular dystrophy
|
|
Sex-linked recessive inherited disease, males are most exclusively affected, 1/3500 boys, diagnosed between age 2-10, muscle weakens, first pelvic muscles affected, then muscles of shoulder and head, rarely live over 20 years.
|
Duchenne muscular dystrophy
|
|
In Duchene dystrophy, Fibers lack a submembrane protein called ________
|
dystrophin
|
|
inherited disorder in which the muscles contract but have decreasing power to relax. With this condition, the muscles also become weak and waste away.
|
Myotonic dystrophy
|
|
Myotonic dystrophy can cause
|
mental deficiency, hair loss and cataracts.
|
|
The myotonic dystrophy gene, found on ___________, codes for a protein kinase that is found in skeletal muscle, where it likely plays a regulatory role.
|
-chromosome 19
|