Human A&P 120
Mar. 2, 2008 REVIEW
OUTLINE for EXAM II
MATERIAL TO REVIEW from EXAM I:
From
LAB--BIOETHICAL PRINCIPLES: be able to apply
A.
AUTONOMY-- individual choice/freedom;autonomy of action should
not be subjected to controlling constraint by others
B. NON-MALEFICENCE:
Above all, do no harm; the first medical principle
C. BENEFICENCE--relationship
to others not just self; oft cited as the 2nd medical principle -- 1. Basic
version: help others only if they want help
-- 2. Strong version=PATERNALISM: higher authority enforces its idea of good
D. JUSTICE--equal
or fair treatment, equal rights, equal goods:
-- 1. Egalitarian--equal goods
-- 2. Libertarian--equal rights/freedoms
WHY needed?
There are optimal states for many things such as water content, temperature, etc.
1. HOW to keep at optimum? Basic Negative
Feedback System!
--VARIATIONS:
a) Dual effector control: 2 effectors that have opposite corrective effects
(e.g., furnace, airconditioner), or 1 effector that can be boosted or
inhibited--e.g., control by parasympathetic va sympathetic nerves);
b) effectors may be behaviors, e.g., seeking warm spots;
B. REGULATED CHANGE--not
everything has a constant optimum
WHY? Many
types of change are useful: growth, puberty, fight-or-flight, cycles, new
situationsÉ
HOW? 2
different mechanisms:
1. RESET System: changes the set point of a negative feedback system.
--a) temporary emergencies: e.g., fever;
stress
--b) cyclical "clocks": e.g., sleep/wake
cycle and hypothalamus SCN clock
2.
POSITIVE FEEDBACK System--one which accentuates a change
rather than reducing it.
Sometimes this is not adaptive but a dangerous malfunction. BUT sometimes it
can be useful for desired rapid changes: e.g., nerve APs!!!
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1. DELAY PROBLEM: Over and/or Undercompensations!
Delay problems are INHERENT
in a simple feedback system because there are always delays in getting a signal
from the disturbed state to the effector's response; if delays are too long
and/or disturbance too fast, the system may oscillate (over and
under-compensation)
-- What to do
about delays?
ANTICIPATION system --one which activates a feedback system before the disturbance
changes a regulated state; may use a sensor to measure the oncoming disturbance rather than the state itself. May be
innate physiology or learned behaviors. Examples: role of Motor
Cortex; Cerebellum; Memory in general
2. NEW-SITUATION PROBLEM: existing feedback system may not work well at high
altitude, with new diet or activity regime, etc. Solution =
ACCLIMATIZATION
or "ADAPTATION" system: change
effectiveness/capacity/ability of feedback component. E.g., buy a bigger air conditioner if
the climate is getting too hot for your old one
A. 2 LEVELS of EXPLANATION
in Biology: see lecture &
reading examples
1. "Proximate" or
mechanistic: "as is"; "how
does it work" analysis. Example: how
sensors "adapt"
2. Evolutionary=historical/selective reason; "why did it end up
this way" E.g, WHY sensors
"adapt"
B. Basic steps in Evolution
by Natural Selection -- review
if needed
–How
GENES are regulated by PROMOTERS & transcription proteins--apply
to MEMORY, hormones!
--LOCK and KEY concept for PROTEINS and molecules that they bind!
--Basic tissue
types and how they make organs
SELF-REGULATION:
Whole-Body Regulatory Systems
OVERVIEW: 1.
Old vs. new ideas: 3-part interaction of Neural, Endocrine, Immunal
2. HIERARCHICAL/distributed REGULATION!! Intrinsic vs Extrinsic multiple levels: Why this is important! Robotics, governments, human body--analogy of Individual->City govt->Count Govt-->State govt->Federal govt
I.
NERVES, NERVOUS SYSTEM
A.
OVERVIEW: Cells
1. NEURONS: know basic structure/parts (dendrites, cell body,
axons, axon ending with synapse)
2. GLIAL (specialized connective):
nourish, assist neurons; insulation--myelin speeds up signals;
--ORGANIZATION: CNS (brain, spine) and PNS in (sensory) and out (motor)=somatic, parasympathetic, sympathetic
--Study Methods: can study individual cells, and brain regions with scanners, stimulators
B. SIGNALS / COMMUNICATION: ELECTRICAL
NEURON
MEMBRANES: have leak
channels; gated channels; Na-K ATPase pump
1. RESTING
POTENTIAL, -70mV: a) Na/K ATPase pump -- moves 3Na+ out and 2K+ in
per cycle: so EXTRACELLULAR fluid
is dominated by Na+, INTRACELLULAR fluid by K+
b) Cell PROTEINS / DNA are negatively charged and trapped INSIDE the cell
c) Na+ has both ELECTRICAL and DIFFUSION gradient inwards, but gates are closed
d) K+ freely moves out through LEAK channels, but held
mostly inside
by negative charges
2. ACTION POTENTIAL (AP):--uses "VOLTAGE-GATED" channel proteins:
|
a) DEPOLARIZATION: some sort of stimulus causes Na+ to enter the neuron (via
elect. Attraction and diffusion); cell voltage rises above -70 mV IF cell voltage
does not reach its threshold,
some K+ leaves and cell goes back to resting; but if it does reach threshold (about -50mV), then b)---> |
b) AP RISE: Positive feedback propogation occurs: at -55mV, Na+
channels snap OPEN. More Na+ to
conduct/diffuse in. This cause nearby channels to reach -55 mV and to open.
And so on. Thus an all-or-none voltage spike (AP)
(about +30mV) propagates down
the cell |
|
c) REPOLARIZATION: at +30 mV, Na+
channels CLOSE and K+ channels
OPEN. K+, which is higher in the cell, then moves out by
conductance at first (repelled by positive charge of cell) and diffusion
later: |
d) Recovery When cell returns to resting
potential (-70mV), all channels close, and the Na/K pump
restores the original Na/K gradients . |
3. GRADED POTENTIALS occur in neurons where there are no voltage-gated channels; other channels let ions flow in but these then decay over distance.
C. SIGNALS / COMMUNICATION: SYNAPTIC TRANSMISSION: axon ending
1) Stimulus: AP
arrives ; 2) Ca++ channels open, and Ca++
ions flow (conduct) in; 3) Ca++ triggers exocytosis of neurotransmitter
(NT) vesicles produced by neuron; 4) Diffusion across synaptic
cleft; 5) Receptor binding
; 6) Receptor action, e.g.,let
Na into target cell: see details below*
7)
Shut-off: NT removed by reuptake
transporter, or enzymatic
breakdown
*Steps 5-6: RECEPTOR DETAILS: "lock and
key" analogy:
a)
Fast Excitatory: simulate the target by opening chemical-gated Na+
channels;
b)
Fast Inhibitory: inhibit the target by opening chemical-gated K+
or Cl- channels;
c)
Slow Modulating--"reprogram"
the target (altering activity of its proteins and/or genes)--
via
receptor-enzyme-2nd
messengers
More on RECEPTOR binding:
1)
"Same-key-different-locks" concept!! Acetylcholine (ACh) example: somatic/motor
nerves use ACh to stimulate skeletal muscles via fast Na channel; parasympathetic nerves use ACh to nhibit HEART via slow opening of K+ channels.
2)
Agonist and antagonist drugs:
AGONISTS mimic a natural NT, but may persist longer; ANTAGONISTS block a
natural NT's actions.
EXAMPLES of KEY NTs and DRUGS
1)
Glutamate = most common
fast excitatory (via Na channels): <---MSG = agonist; ketamines=antagonist
2)
GABA = widespread fast
inhibitory (via Cl- channels)
<---ethanol is agonist!!
So is [Valium]
3)
Serotonin: modulator,
prolonged stimulation of mood/serenity neurons <----Prozac blocks reuptake
--associated
with serenity/calmness; anti-aggression/anti- anxiety; depression if too low
4)
Adenosine from LAB= inhibitory (via K+ channels) <----caffeine is antagonist
SEE MORE LATER and from LAB
D.
INFORMATION and INTEGRATION:
--ALL-or-NONE ACTION POTENTIALS: how get GRADED information or commands?
1) Information sent by FREQUENCY of APs--how weak vs strong stimuli cause this
2) Multiple neurons to/from organs: example of MOTOR UNITS each controlling only a
small part of a muscle. Note: fineness of muscle motions requires many motor
units Émale vs female
--DECISIONS made by