Monday, December 6, 2010

Specific Neurotransmitters

Acetylcholine
Chemical Structure: an ester of acetic acid and choline ("cholinergic")
Place of Action: Both CNS and PNS; only transmitter used in motor movement; important nervous transmitter
Main Effects of Postsynaptic Neurons: excites muscles; assists our brain and nervous action
Disorders (Too Much/Little): memory loss (Alzheimer), and muscle fatigue/weakness (myasthenia gravis)


Norepinephrine
Chemical Structure: Adrenergic
Place of Action: sugar stores (in all cells), 
Main Effects of Postsynaptic Neurons: increased heart rate
Disorders (Too Much/Little):

Dopamine
Chemical Structure:
Place of Action:
Main Effects of Postsynaptic Neurons:
Disorders (Too Much/Little):

Serotonin
Chemical Structure:
Place of Action:
Main Effects of Postsynaptic Neurons:
Disorders (Too Much/Little):

GABA
Chemical Structure:
Place of Action:
Main Effects of Postsynaptic Neurons:
Disorders (Too Much/Little):

Glutamate
Chemical Structure:
Place of Action:
Main Effects of Postsynaptic Neurons:
Disorders (Too Much/Little):

Glycine
Chemical Structure:
Place of Action:
Main Effects of Postsynaptic Neurons:
Disorders (Too Much/Little):

Endorphins
Chemical Structure:
Place of Action:
Main Effects of Postsynaptic Neurons:
Disorders (Too Much/Little):

screw it. just gonna take a hit for the 1-2 questions this will be on the test. not wasting an hour looking this up

Sunday, December 5, 2010

Neuroanatomy Unit III Sect. I

Going clear back to the beginning of Unit III and working my way through. Hopefully I've made it easy to understand where I'm at.


 Name three main functions of nervous system.
Sensory input- gathering information
Integration- interpretation
Motor output- making the body respond to those stimuli


 Describe anatomical organization of nervous system (central and peripheral) and
its components.
Central Nervous System (CNS)- brain and spinal cord
Peripheral NS- everything that used to communicate with the brain and spine


 Describe physiological organization of peripheral nervous system (afferent, efferent). Explain the role of afferent division of PNS and compare its visceral and somatic components. Explain the role of efferent division of PNS and compare its autonomic (visceral) and somatic components. Name two branches of autonomic nervous system and explain their roles in regulation of body functions.
PNS has two parts:
Afferent- carrying impulses to the CNS, has both conscious and unconscious components
Efferent- carrying impulses to the PNS, also has intentional (ie somatic) and automatic parts
The autonomic part is then split into sympathetic (emergencies) and parasympathetic (relaxation) systems


 Describe the cellular components of a neuron (body, axon, dendrite, axon hillock
and synaptic knob).
Neuron body- contains nucleus and organelles, conducts charge to some degree
Axon- carries impulse away from neuron body
Dendrite- carries impulse into neuron body
Axon hillock- where axon begins, sending off the initial charge
synaptic knob- end of axon, releasing neurotransmitters when activated


 Describe three types of neurons based on their structure, explain their function.
Unipolar- axon divides into two, found in the brain and spine
Bipolar- has both a long axon and a long dendrite, found in eye and nose (sensory)
Multipolar- many small dendrites and a long axon, most common


 Give functional classification of neurons (motor, sensory and interneurons). Give
example using reflex arc.
Word for word:
Sensory- afferent neurons
Motor- efferent neurons
Interneurons- associated neurons
Touching a stove triggers reflexive arch, the hard wired, unconscious response necessary when an immediate response is required.


 Explain the following terms: electricity, voltage (potential difference), current, resistance, polarity, electrical gradient, and chemical gradient.
Electricity- stationary or moving electrons and protons
Voltage- electric potential: the difference in electrical charge between two points in a circuit expressed in volts
Current- a flow of electricity through a conductor; "the current was measured in amperes"
Resistance- a material's opposition to the flow of electric current
Polarity- having a pair of equal and opposite charges
Electrical gradient- the difference in electrical charge (valence) across the membrane
Chemical gradient- a difference in the bulk concentration of an ionic species on either side of the membrane


 Name different types of plasma membrane ion channels and explain how they function; give examples. Compare intracellular and extracellular concentration of sodium, potassium and chloride ions. Comment on the membrane permeability for these ions at rest. Explain physiological bases for resting membrane potential.
What ion is mostly responsible for it? Is the resting membrane potential a truly
restful state or is it an active process? What is the role of sodium-potassium
pump in this process? What is the numerical value of resting membrane potential
in a neuron?
There are passive and active ion channels. Passive means that the ions flow with the gradient (electrical and chemical). Most of the time the sodium (Na) and potassium (K) are flowing in these directions. Since these ions (Na and K) they don't want to go up the gradient, they have to be actively transported by pumps in order to reset the cell.
Normally there is too much K inside the cell and too much Na outside the cell. This is what creates the gradients.
Potassium is responsible for the resting membrane potential because it flows out more than sodium flows in.
Maintaining a resting state requires a good effort because these two ions are always trying to slip in/out and having to be pumped back.
Resting membrane potential= -70mV

Unit III for my own Reference

Unit III - Neurophysiology
 Name three main functions of nervous system.
 Describe anatomical organization of nervous system (central and peripheral) and
its components.
 Describe physiological organization of peripheral nervous system (afferent,
efferent).  Explain the role of afferent division of PNS and compare its visceral
and somatic components. Explain the role of efferent division of PNS and
compare its autonomic (visceral) and somatic components.  Name two branches
of autonomic nervous system and explain their roles in regulation of body
functions.
 Describe the cellular components of a neuron (body, axon, dendrite, axon hillock
and synaptic knob).
 Describe three types of neurons based on their structure, explain their function.
 Give functional classification of neurons (motor, sensory and interneurons).  Give
example using reflex arc.
 Explain the following terms: electricity, voltage (potential difference), current,
resistance, polarity, electrical gradient, and chemical gradient.
 Name different types of plasma membrane ion channels and explain how they
function; give examples.  Compare intracellular and extracellular concentration of
sodium, potassium and chloride ions.  Comment on the membrane permeability
for these ions at rest.  Explain physiological bases for resting membrane potential.
What ion is mostly responsible for it?  Is the resting membrane potential a truly
restful state or is it an active process?  What is the role of sodium-potassium
pump in this process?  What is the numerical value of resting membrane potential
in a neuron?
 Define depolarization and hyperpolarization and explain how they are affected by
the change in the membrane permeability of different ions.
 Explain how is the permeability of sodium and potassium voltage-gated channels
regulated.  Describe three states of sodium voltage-gated channels.
 Define action potential.  Name the phases of action potential in a neuron. Explain
their ionic bases. Where action potential is normally generated? What is the role
of sodium-potassium pump in this process?
 Explain the “All or None” principle. Give examples of subthreshold and threshold
impulses.  Will the stronger stimulus case a larger action potential? How is the
strength of a stimulus transmitted in the nervous system?
 Define absolute and relative refractory period.  Explain the ionic bases for these
phenomena.
 Define the terms insulator and conductor.  Give examples.
 Explain how the action potential is spreads along the axon, why does it normally
spread in only one direction, why it is said to be self-propagating and nondecremental?
 Explain the structure and function of myelin.  Compare the speed of conductance
in myelinated and unmyelinated axons.  Explain physiological bases for saltatory
conduction.
 Compare A, B and C fibers.
 Explain what causes action potentials? Is it a spontaneous change or is it caused
by the change in the environment?  Compare graded and action potential.  Name
two types of graded potentials.  BIO 231  Dr. Tanya McVay
 Define receptors and classify them according to the type of energy to which they
respond.  Describe how generator potentials are produced and explore their effects
on action potential production.
 Compare phasic and tonic receptors. Define sensory adaptation.
 Explain how different types of stimuli are conveyed to CNS: type of sensation,
place of origin of sensation and strength of stimulus.
 Explain how the stimulus is passed from one neuron to the other.  Compare
chemical and electrical synapses.
 Identify the parts of the synapse. Explain the mechanism of synaptic transmission.
What is the role of calcium ion in this process?  What is the role of
neurotransmitter?
 Explain how is synaptic transmission terminated.  What are the means by which
the neurotransmitter is removed from the synaptic cleft?
 Explore the following neurotransmitters based on their chemical structure, place
of action, main effects on postsynaptic neurons: Acetylcholine, norepinephrine,
dopamine, serotonin, GABA, glutamate, glycine and endorphins.  Name disorders
associated with their inadequate production.
 Compare excitatory postsynaptic potentials and inhibitory postsynaptic potentials.
 Name three types of synapses based on their location on a neuron.  
 Compare graded potentials (generator and postsynaptic) and action potentials.
 Define neuronal pool and explain how neuronal recruitment relates to the strength
of the stimulus.  Name four types of neuronal circuits.  Explain the difference
between the serial and parallel processing.

Pancreas and Minor Endocrine Glands

Ok so since the final is tomorrow I guess that I should start putting up the other sections!


 Explore gross and microscopic anatomy of pancreas. Compare hormones to
enzymes produces there. List hormones of the pancreas*. Recall the normal
fasting level of blood glucose and explain how insulin* and glucagon* maintain
this concentration. Relate insulin insufficiency to diabetes type I and II. What are
the symptoms in patients with this disorder and how do they relate to insulin
function? What preventative measures can be taken by diabetic patients and
people at risk?
Anatomy- because the pancreas has both endocrine and exocrine glands it has both types of setup on the microscopic level. The outside of cell groups are exocrine, that all circle/focus around a central canal that they disperse their hormones into. The middle area, aka the Islets of Langerhans, is an endocrine area.
Hormones of pancreas:
     Glucagon- raises blood sugar levels. Breaks down glycogen, fatty acids and fat into sugar. Acts on 2nd messenger (cAMP).
     Insulin- "Store fuel for later." Activates tyrosine kinase in cells that makes them increase glucose uptake, increase glycogen synthesis, increase ATP amounts from glucose, increase amino acid uptake and protein production, and increase fat production.
     Somatostatin- an inhibitory hormone
     Pancreatic polypeptide- self regulate the pancreas secretion activities
Normal fasting sugar level- 80mg/dL
Insulin and glucagon maintain homeostasis through humoral regulation. Not much more to say on that...
Diabetes mellitus- lack of insulin production, forcing body to use fatty acids as food. Manifests in frequent peeing, sugary urine, constant thirst, and constant hunger. All of this is because the body cannot hold onto sugars.
     Type 1- autoimmune destruction of pancreatic B cells (the insulin producers)
     Type 2- abnormal insulin that is either not recognized or is destroyed by immune system
Preventative measures: lose weight (most important since obesity and diabetes work together well) by eating healthy and exercising. Remind them that they have the power to keep their diabetes under control and the horrible things that can happen if they don't :D


 List minor endocrine glands, their hormones and major effects on the body.
The only list I could find to address this is under the heading, General Organization of the Endocrine System (Unit IV Lec. I). If there are more please let me know.
Adipose tissue- lipton (appetite control) and resistin (controls energy homeostasis)
Intestinal wall- cholecystokinin (triggered by fats, tells gallbladder to release digestive enzymes)
Stomach- gastrin (stimulates gastric acid production), histamine (triggers inflammatory response), endorphins (happy drug), serotonin (another happy hormone), cholecystokinin (fat digestion), and somatostatin (inhibitory hormone)
Kidney- erythropoietin (red blood cell production) and calcitriol (tells body to absorb calcium and put it in the blood)
Heart- Atrial natriuretic peptide and brain type natriuretic peptide both lower blood pressure
I'm pretty sure she said that we only have to know the main one but since she didn't have the "most important one" in her notes I covered all of them.

Tuesday, November 30, 2010

Study Guide for Dec 1 Quiz

Quiz 7 (or something)- Happening December 1


So I'm skipping a large part of the study guide, going straight to the part that has to do with this week's test. Call it egotistical but I want a good grade. Later I'll go back at least to section III before the final (since apparently III and IV make up roughly 70% of the test).

 Name factors that determine strength of physiological response caused by
hormone.
Strength of hormonal a response is dependent on how receptive the target cell is, and how concentrated the dosed hormone is released in the blood (the more the greater the response).

 List the three ways the body regulates hormonal production. Explain humoral,
neural and hormonal regulations of hormone production. Compare negative and
positive feedback mechanisms. Give examples of hormones in each category.
The body regulates hormones in these three ways:
1. Humoral stimulation, or in other words, the body constantly "tasting" the blood to make sure it has the right composition.
2. Neural stimulation- this system generally just tends to do it's thing automatically. By sending out it's own transmitters it can manipulate the endocrine system.
3. Endocrine stimulation- One endocrine gland affects another endocrine gland, which affects another endocrine gland. In a snowball sort of way, every endocrine gland can influence another.
Fortunately there are blocks in place to prevent it from getting too unruly. Positive Feedback simply means that the endocrine glands feed off another in a self perpetuating cycle. Negative Feedback conversely means that one endocrine gland in the perpetuating loop has had enough and tells the others to close shop.

 Explain the types of hormone interaction at the target cells.
Easy! McVay loves to cover this one as it's the basis for hormone-cell interaction. Simply put, amino acid-based hormones (amino acids, peptides, poly-peptides, and proteins) are all dissolved in the plasma of the blood and attach to the surface of the target cell when passing by. On the other hand, the more complex molecules like steroids and other fatty molecules (anyone know any others?) require special protein transports to get to their destinations. Upon arrival steroids will pass through the membrane (because like dissolves/passes through like) and begin transcription.

 Name an endocrine gland responsible for neural regulation of endocrine system.
Explain how releasing and inhibiting factors regulate hypophyseal activity
(hypothalamo-pituitary axis). List hormones of hypothalamus* and their effects
on pituitary gland.
Hypothalamus regulates both neural and endocrine systems. Apparently the pituitary gland is the puppet of the hypothalamus, doing its bidding like the mind controlled servant that it is. The two function together quite well- the hypothalamus releases hormones that switches both anterior and posterior pituitarys on, the anterior pituitary releases its hormones into the body, the hypothalamus is satisfied with the reaction and produces inhibiting "factors" (hormones).
Listing the hormones and their effects is well above my pay-grade. (will probably come back to this)

 Recall anatomy of pituitary gland and hypophyseal portal system. Explore the
differences between neurohypophysis and adenohypophysis.
Not only does the hypothalamus reign supreme over the pituitary gland but it does it in two separate ways: through hormonal regulation (on the anterior pituitary) and neural stimulation (on the posterior pituitary, which I believe does have a small hormone gap the jump as part of the process, which then starts off the neural response).
Adenohypophysis= anterior pituitary
Neurohypophysis= posterior and is considered part of the hypothalamus because of its neuronal connection.

 List hormones of anterior pituitary* and explain their role in regulation of
endocrine system. What abnormalities result from inadequate production of these
hormones? Based on the function of these hormones, predict the symptoms in
patients with these abnormalities.
All hormones of the anterior pituitary (AP) are called Adenohypophysis. They are also more commonly referred to as trophic hormones, and are listed next:
Growth hormone (GH)- not only affects epiphyseal plates but every cell in the body. Causes production of somatomedins by muscle, liver, and bone (also promotes growth and mediates GH). Too little can lead to pituitary dwarfism. Too much causes gigantism (children) and acromegaly (adults).
Prolactin- stimulates milk production and parental behavior (aka child attachment). Hypothalamus sends Prolactin-releasing hormone (PRH, a seratonin) or Prolactin-inhibiting hormone (PIH, a dopamine) to anterior pituitary (AP) as part of regulation. Prolactin is known to cause tumors in the AP, which can cause headaches, inappropriate lactation, off-beat menstrual cycles, and male impotence.
Adrenocorticotropic hormone (ACTH)- stimpulates production of glucocorticoids (cortisol, corticosteron) by the adrenal cortex (which is also partly covered later!). Hypothalamus releases corticotropin releasing hormone (CRH) to increase ACTH production, which follows the circadian rhythm. In other words, ACTH helps as wake up in the morning and taper off at night by flowing or limiting the amount of energy to us, and it is all controlled by CRH from the hypothalamus.
Thyroid stimulating hormone (TSH)- released by AP. As usual it starts with hypothalamus that releases thyrotropin-releasing hormone, which in turn causes AP to release TSH, which activates thyroid, which makes thyroxin that affects target cell and turns off (negative response) AP and hypothalamus.
Gonadotropins- includes Luteinizing Hormone (LH, promotes synthesis of gonadal hormones in ovaries and testes) and Follicle-Stimulating Hormone (FSH, promotes development of egg and sperm). Both are only used after puberty starts, and are activated by Gonadotropin-Releasing Hormone (GnRH).

Something that I've noticed is that everything that comes from the hypothalamus has "Releasing Hormone" as part of the name. This makes it easy to identify whether it is coming from the hypothalamus or the AP.

 List hormones of posterior pituitary*. Describe the role of oxytocin during labor
and milk ejection. Explain why the production of oxytocin* increases during/
after labor. Explain the role of ADH in fluid/electrolyte balance. What
abnormalities result from inadequate production of this hormone? Apply your
knowledge of effects of ADH on target cells to predict symptoms in patients with
inadequate production of this hormone.
The two major hormones of the posterior pituitary are Oxytocin and Antidiuretic hormone (ADH).
Oxytocin is important during birth because it increases uterine contractions via a positive feedback cycle that begins with dilation of the cervix. It is important during breast feeding because it causes the smooth muscle to push the milk out. Lastly, it is the bonding hormone for moms, causing them to become more effectionate with the newborn. This can be helpful when the mother experiences post-partum depression, getting a distant mom to start feeling close with the newborn.
In males it causes ejaculation lol.
Antidiuretic means "retain water" ("against peeing"). When osmorecepters taste too many electrolytes in the blood (humoral regulation) then ADH is sent to the kidneys to retain water. More water is absorbed back into the body and extra concentrated pee is produced. ADH also causes vasoconstriction, raising blood pressure.
If a person cannot produce enough ADH then there is a good chance they will develop diabetes insipidus, where the body can't produce concentrated urine and constantly suffers from an electrolyte balance.
Too much ADH leads to sodium/electrolyte deficiencies, water retention, and other problems having to deal with holding onto too much water and not enough other stuff.
Both posterior pituitary gland hormones are produced in the hypothalamus (paraventricular nucleus and supraoptic nucleus, which are names of different types of nuclei that are both found in the hypothalamus). Both also use the PIP2 mechanism to affect the target cells.


 Explore anatomy of thyroid gland. List three hormones* produced there. Explain
how thyroid hormones (T3, T4) are produced and regulate metabolic rates in the
body. Apply your knowledge of effects of thyroid hormones on target cells to
predict symptoms in patients with inadequate production of these hormones.
What are these abnormalities?
It's below the Adams apple on both sides with a small connection between both sides. Study the images to get the microscopic structure.
It produces triiodothyronine (T3) (10%), thyroxine (T4) (90%) and calcitonin. Iodine is mixed with the colloid inside of the thyroid gland to produce T4. T3 is much more powerful than T4 although it is produced much less frequently, but is converted frequently to T3, especially in the kidneys and liver. Although it is an amino-based hormone it is one of the few that cannot travel alone in the bloodstream and must attach to other proteins (usually liver proteins like albumin and thyroxin) to reach target cells (and affects the nucleus of the celll). It is required by all cells, and is used to increase metabolic activity. This means it throws the cell into gear, consuming oxygen, sugars, ATP, fat, and producing more heat.
It also regulates growth and development, which is important the fetus and infants (lack= cerebral damage).
Deficiencies manifest in Simple Goiter, dwarfism, and retardation.


 Explain the role of calcitonin* and parathyroid* hormone in regulation of calcium
blood concentration. Predict the outcomes for the patient with hypoparathyroidism.
Calcitonin and parathyroid work constantly to keep the blood concentrations of calcium in check. Calcitonin targets osteoblasts, telling them to take calcium out of the blood to store in bone. Conversely, parathyroid hormone targets the osteoclasts, making them dissolve bone for use in the blood. It also tells the kidneys to hold onto calcium during filtration.
Hypothyroidism is a deficiency of calcium in the blood. This affects everything that uses calcium, including muscles, brain, and nervous system. It's used a lot!

 Explore gross and microscopic anatomy of adrenal gland. List three zones of
adrenal cortex and give examples of hormones* produced there. What is the role
of aldosterone* in regulating blood pressure and electrolyte balance? Apply you
knowledge of aldosterone’s function to explain symptoms of Conn’s syndrome.
The outer section is called the cortex, the inner the medulla. Each part produces very different hormones.
Three zones of cortex:
1. Zona glomerulosa- mineralcorticoids
2. Zona fasciculata- glucocorticoids
3. Zona reticularis- gonadocorticoids
All are considered "corticosteroids"
Aldosterone causes water retention (same effect as ADH) by telling the kidneys to retain sodium- water follows the sodium (Na+) along the concentration gradient. It also tells the kidneys to get rid of potassium (K+). Consequently the extra fluid in the system raises blood pressure.
Conn's syndrome is overproduction of Aldosterone, which leads to too much water and Na+ in the body and a lack of K+. This causes hypertension, edema, and muscle weakness (action potential can't be generated).


 Explain the circadian rhythms in production of cortisol*. Apply you knowledge of
hormone’s effects to explain symptoms of Addison’s and Cushing’s syndrome.
Cortisol is released in accordance with our circadian rhythm, putting out more while we're awake and turning off at night (or whenever we sleep...). It gets the body to take energy from all the sources, sugar, fat, and proteins, and use it for activity. Production is regulated by ACTH (found in the anterior pituitary section), and returns a negative feedback to ACTH. Oddly enough cortisol also suppresses our immune response.
Addison's syndrome (lack of adrenal gland hormones)- hypoglycemia, hyperpigmentation (don't know why...), dehydration, and excessive acid and K+ in blood.
Cushing's syndrome (excessive corticosteroids)- excessive sugar in blood, obesity, poor wound healing, hypertension, stretch marks, and masculine hair growth.




 Explain how hormones of adrenal medulla* help body to cope with stress. What
abnormality results from overproduction of these hormones?
Epinephrine (80%) and norepinephrine (20%) cause an increase in heart rate and contractibility, increased blood pressure, peripheral vasoconstriction (which is just another way of increasing blood pressure...), and hyperglycemia. Glucocoricoids are much more effective but these are good for quick situations.
Overproduction can be cause by tumors on adrenal medulla, leading to hyperglycemia, tachycardia (fast heart rate), and hypertension.
All hormones of adrenal gland prepare for stress!

Readers, sorry if this was a long dry read! It was definitely a long, dry write. There are a lot of hormones to be known for this quiz. It's crazy how much material can pile up from not having a quiz for two weeks.
Hang in there though! Term is almost over :)

Friday, November 26, 2010

For my own reference

Just putting all the sectino IV study guide here for my own quick reference

Unit IV
* For all hormones mentioned below, study:
 Site of production
 Chemical structure (amino acid, protein, steroid)
 Target cells
 Type of receptors on the target cells
 Mechanism of action
 Effects on the target cells
 Regulation of production
It might be worthwhile to create a table with these categories and fill it out as you
prepare for class.
 Define the function of the endocrine system
 Compare endocrine vs. exocrine glands. What are the paracrine and autocrine
cells? Give examples of the glands that function exclusively in endocrine mode,
endocrine and exocrine modes, have endocrine and neural components, and have
minor endocrine components.
 Define hormone and name its main characteristics. Classify hormones based on
their chemical structures.
 Explain why only the target cells are sensitive to the hormonal stimulation. Give
examples of effects in target cells induced by this stimulation.
 Name mechanisms of action by which hormones stimulate target cells. What
properties of hormones determine whether they stimulate intracellular or surface
receptors?
 Explain tyrosin kinase mechanism of action (bypassing 2nd messenger). Give
examples of hormones that act that way.
 Explain 2nd messenger mechanism of action. What is the role of cAMP? Give
examples of hormones that act that way.
 Explain PIP/calcium mechanism of action (3rd messenger). What substances act
as 2nd and third messengers? Give examples of hormones that act that way.
 Explain intracellular receptor stimulation mechanism of action (gene stimulation).
Give examples of hormones that act that way.
 Name factors that determine strength of physiological response caused by
hormone.
 List the three ways the body regulates hormonal production. Explain humoral,
neural and hormonal regulations of hormone production. Compare negative and
positive feedback mechanisms. Give examples of hormones in each category.
 Explain the types of hormone interaction at the target cells.
 Name an endocrine gland responsible for neural regulation of endocrine system.
Explain how releasing and inhibiting factors regulate hypophyseal activity
(hypothalamo-pituitary axis). List hormones of hypothalamus* and their effects
on pituitary gland.
 Recall anatomy of pituitary gland and hypophyseal portal system. Explore the
differences between neurohypophysis and adenohypophysis.
 List hormones of anterior pituitary* and explain their role in regulation of
endocrine system. What abnormalities result from inadequate production of these
hormones? Based on the function of these hormones, predict the symptoms in
patients with these abnormalities.
BIO 231 Dr. Tanya McVay
 List hormones of posterior pituitary*. Describe the role of oxytocin during labor
and milk ejection. Explain why the production of oxytocin* increases during/
after labor. Explain the role of ADH in fluid/electrolyte balance. What
abnormalities result from inadequate production of this hormone? Apply your
knowledge of effects of ADH on target cells to predict symptoms in patients with
inadequate production of this hormone.
 Explore anatomy of thyroid gland. List three hormones* produced there. Explain
how thyroid hormones (T3, T4) are produced and regulate metabolic rates in the
body. Apply your knowledge of effects of thyroid hormones on target cells to
predict symptoms in patients with inadequate production of these hormones.
What are these abnormalities?
 Explain the role of calcitonin* and parathyroid* hormone in regulation of calcium
blood concentration. Predict the outcomes for the patient with
hypoparathyroidism.
 Explore gross and microscopic anatomy of adrenal gland. List three zones of
adrenal cortex and give examples of hormones* produced there. What is the role
of aldosterone* in regulating blood pressure and electrolyte balance? Apply you
knowledge of aldosterone’s function to explain symptoms of Conn’s syndrome.
 Explain the circadian rhythms in production of cortisol*. Apply you knowledge of
hormone’s effects to explain symptoms of Addison’s and Cushing’s syndrome.
 Explain how hormones of adrenal medulla* help body to cope with stress. What
abnormality results from overproduction of these hormones?
 Explore gross and microscopic anatomy of pancreas. Compare hormones to
enzymes produces there. List hormones of the pancreas*. Recall the normal
fasting level of blood glucose and explain how insulin* and glucagon* maintain
this concentration. Relate insulin insufficiency to diabetes type I and II. What are
the symptoms in patients with this disorder and how do they relate to insulin
function? What preventative measures can be taken by diabetic patients and
people at risk?
 List minor endocrine glands, their hormones and major effects on the body.

Thursday, November 18, 2010

Act 1: Scene 1

Alright, maybe my relationship with A&P is more love than hate, and sometimes being a little more theatrical makes life easier to deal with. In a lot of ways I really do love learning about the body. There is so much to it and yet it all works together in near-perfect harmony- it is an interesting and fascinating creation. Still, A&P is a crazy, in-depth class that is (I think) fairly rapidly teaching many students here at OIT a great deal about the body.

For those of you who are way to brain-fried to even remember what A&P stands for, it has the long and drawn out title of Anatomy and Physiology. The anatomy is part of that represents "gross anatomy," or for some, "memorizing all the parts of the body while leaving no room in one's head for learning how they work together."

Physiology is, of course, how those body parts work together. It's learning how ion channels make muscles and nerves work. It's memorizing laundry lists of chemicals and other microscopic... things and how they interact. Oh, and it's the hard part of A&P.

One of McVay's favorite questions to ask in lecture (lecture=physiology, lab=anatomy) (sorry for bringing math into this...) is, "Why do you give a damn?" -usually when trying to stress the importance of our knowing the current material for future careers. Sometimes though, even after she's explained how this trippy concept works and how it applies to the drugs we will be giving our future patients (just as an example), it is still hard to always care. Not because it isn't interesting, but because there is just so much physiology to have to learn and understand at the end of every day.

Well, that and she keeps quizzing us on some really crap stuff.
Which is why I have created this blog- to help all those (and especially myself!) solidify all the ideas and concepts that we have to know. To give my fellow students & friends another tool in their arsenal for combating the monster. To make sure that nobody (namely me) has to ever say again, "I can't believe she's quizzing us on that paragraph from last weeks material! How am I supposed to remember a week ago?" Because as Gandalf of LOTR could relate, some days (of A&P) feel as long as life of the earth.

Throughout this blog I will mainly be covering McVay's study guide. I will attempt to answer each part in great detail and add as much as possible from what she says in class (and maybe other sources too if we're all lucky).

I would love any additional insight to this joint study guide that anyone has to offer. Please feel free to make comments, correct me on anything, or bring any new insight to the table.

A&P, you're going down.
~Jared