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Cardiovascular System in Vertebrates (notes)
Consists of heart, vessels, blood
Heart has…
1/2 atria chambers that receive blood
1/2 ventricle chambers that pump OUT blood
Many have two other chambers
Sinus venosus — receiving upstream from atrium
Conus Arteriosus — directs blood out of heart
mammals lose as they develop
Arteries carry blood away from heart
Branch into arterioles which then branch into capillaries
Capillaries are microscopic, sites of exchange, leaky
tight junctions are not so tight
Capillaries join together to form venules which then join to form veins
Veins carry blood toward heart
Circulation in Actinopterygii (notes)
Two chambered heart (one atrium, one ventricle) on ventral (bottom) side of the body
Blood from body —> sinus venosus (low pressure, low oxygen) —> atrium —> ventricle —> Conus arteriosus (high pressure, low oxygen)
ventricle puts blood under pressure
Blood flows from conus arteriosus into ventral aorta (main artery)
Ventral aorta has four branches on each side that branch upward —afferent branchial arteries
lead into gill arches —> gill filaments —> gill lamellae —> capillaries in gills
Blood passes from afferent branchial arteries to efferent branchial arteries
(high pressure, low oxygen) —> (low pressure, high oxygen) after moving through capillaries
Blood now moves up to dorsal aorta (main artery)
most goes posterior to tail
some goes to brain though
Initially 2 dorsal aortae side by side that fuse into one (just past the gills)
Other arteries that branch from dorsal aorta that go through capillary beds throughout body
low pressure, high O2 —> lost to low pressure, low O2
Low pressure blood moves through body through muscle contractions
Then cycle restarts
Circulation in Frogs (notes)
Three chambered heart (2 atria (left & right, 1 ventricle)
2 Circuits (Double Circulation) IN ALL TETRAPODS
Pulmocutaneous circuit: heart (right) —> respiratory organ —> heart (right)
Systemic circuit: heart (left) —> tissue/organs —> heart (left)
high pressure, low O2 as it leaves right ventricle, goes into capillaries of respiratory organs (lungs/skin), low pressure, high O2
blood goes back into heart to left ventricle with low pressure, high O2, then gets pushed into aorta (main artery) — 2 aorta arches that fuse into 1
Ridges separate sides of the ventricle, there’s slight mixing of blood from left and right sides but not enough to affect their health
Circulation in Reptiles (notes)
Ridge separating ventricles is better developed in non-archosaur reptiles
Similar circulation system to amphibians
Archosaurs have 4 chambered hearts fully separated by walls (ex. crocs, birds, dinos)
Can shunt blood when they dive — stops sending blood to the lungs
shunts pulmonary artery to aorta to BYPASS pulmonary circuit
Right side receives from systemic and pumps into pulmonary circuit
Left side receives pulmonary and pumps into systemic circuit
Circulation in Mammals & Archosaurs (notes)
Four chambered heart (2 atria, 2 ventricles)
Atria receive blood only
Ventricles pump blood
No mixing of O2 rich and O2 depleted blood
Double circulation — restores pressure after blood passes through capillaries
Evolution of vertebrate circulation (notes)
Sharks: 6 aortic/gill arches
Teleost Fish (Actinopterygii): lost 2 front arches
Lung fish: retained arch 2 but lost front arch
6th arch shunts blood through gills/lungs
Amphibians: lost arches 1,2,5
arch 3 separated from dorsal aortae (goes anterior) — carotid artery to brain
arch 4 is aortic arches
arch 6 = pulmonary arteries to lungs
Reptiles (non archosaur): lost arches 1,2,5
arch 3 separated from dorsal aortae (goes anterior) — carotid artery to brain
arch 4 is aortic arches (R & L)
arch 6 = pulmonary arteries to lungs
Birds (archosaurs): lost 1,2,5 fully
LOST left of 4 = aortic arch
arch 3 = carotid artery to brain
right side of arch 4 = aortic artery
arch 6 = pulmonary artery to lungs
Mammals: lost 1,2,5
LOST bottom right of 4 = aortic arch
arch 3 = carotid artery to brain
left side of arch 4 = aortic artery
arch 6 = pulmonary artery to lungs
Subclavian arteries = go to pectoral limbs
Teleost, Amphibians previously posterior
Birds and Mammals now anterior
Mammal — the left subclavian artery branches directly off the aortic arch
Birds — subclavian arteries branch directly from carotid artery
Receives blood from head and upper limbs
Superior Vena Cava
Receives blood from trunk and legs
Inferior Vena Cava
Receives blood from right lung
Right Pulmonary Veins
Receives blood from left lungs
Left Pulmonary Veins
Receives blood from the pulmonary circuit
Left Atrium
Receives blood from the systemic circuit
Right Atrium
Pumps blood to the pulmonary circuit
Right Ventricle
Pumps blood to the systemic circuit
Left Ventricle
Where does left ventricle pump blood out to?
Aorta
Artery that leads blood to the liver
Hepatic Artery
Vein that receives blood from the liver
Hepatic Vein
a different path that leads into the liver and is bound on each end with capillary beds
Hepatic Portal Vessel
Hepatic Portal Vessel and Hepatic Artery exit where?
Through Hepatic Vein —> Vena Cava
Where blood flows to capillary beds in the kidneys
Renal Artery
From where blood goes from capillary beds in the kidney to then after, into the the Inferior Vena Cava
Renal Vein
Blood does NOT move through…
more than one systemic capillary bed or organs
Trace the pathway followed by a short chain fatty acid to a toe cell
Oral cavity
Pharynx
Esophagus
Stomach
Small intestine
Apical PM of mucosa cell
Basal PM of mucosa cell
Interstitial Fluid
Basal PM of capillary cell
Apical PM of capillary cell
Hepatic Portal Vessel
Hepatic Capillary
Hepatic Vein
Vena Cava
Right Atrium
Right Ventricle
Pulmonary Artery
Lung Capillary
Pulmonary Vein
Left Atrium
Left Ventricle
Aorta
Artery in toe
Capillary in toe
Apical PM of Capillary
Basal PM of Capillary
Interstitial Fluid
PM of toe cell
Rhythmic Pumping (notes)
Systole = when blood is pumped from the heart or Contraction
Diastole = when heart fills with blood or Relaxation
Valves prevent backflow of blood in heart
Atrioventricular Valves (AV) = between atrium and ventricles
Semilunar Valves (SV) = between ventricles and arteries exiting the heart (aorta/pulmonary artery)
Lub Dub heart sounds caused by the closing of valves
Lub = atrioventricular valves
Dub = semilunar valves
Cardiac Output
Volume of blood pumped per minute by left ventricle
Cardiac Output = heart rates * stroke volume
Heart rate = BPM
Stroke Volume = blood pumped by left ventricle per contraction
Control of Heart Rhythm (notes)
Myogenic hearts
most mammals/vertebrates
no nerve impulse for every contraction
self rhythm — input from nervous system to modulate what’s going on but they are self excitable
Sinoatrial (SA) node in right atrium sends electrical signal without input from brain causing muscles in atria to contract
Pacemaker
Gap junctions allow small molecules to pass through w/o plasma membranes — where charges move through
Atrium contract before ventricles with a delay of 0.1s — Atrioventricular Node (AV)
electric currents detected at surface —EKG
Neurogenic hearts
nerve impulse required for every contraction of heart
Electrical signals of the heart/brain are…
movement of charges (charged ions)
Arteries and Veins layer makeup
3 layers
outer layer of connective tissue
middle layer of smooth muscle — vasoconstriction and vasodilation
inner layer of single, simple, squamous epithelium called ENDOTHELIUM
When smooth muscle decrease diameter of blood vessel
Vasoconstriction
When smooth muscle relaxes and increases diameter of blood vessel
Vasodilation
Capillary makeup
1 layer of endothelium
tight junctions aren’t very tight
has pores between cells that allow exchange between IF and blood
______ have valves along system to prevent backflow
Veins
Blood Flow (notes)
Flow rate remains constant always because narrower canals have faster Velocity
Velocity
high in arteries
low in capillaries
total cross section area is larger so velocity drops
moderate in veins — regains speed
Blood Pressure = hydrostatic force that blood exerts against a vessel wall
pressure is high in arteries (ventricles creates greater blood pressure which directly move to aorta/artery)
drops as it moves through capillaries and never regained
in veins pressure is NEAR zero
valves prevent backflow
blood flow to capillaries controlled by nerves and hormones
Exchange in Capillary Beds (notes)
O2 and CO2 diffuse down concentration gradient
However small materials can leave through leaky capillary walls as pressure from blood pushes things out
small materials include salts, water, amino acids, and vitamins
concentration of small materials equal inside and outside
large materials include blood proteins
Because large materials aren’t naturally diffusing out, blood proteins stay in blood and contribute to osmotic pressure
Direction of Flow in Capillaries (notes)
Dependent on the balance between hydrostatic pressure and osmotic pressure
Osmotic Pressure depends on solute concentration
overall solute conc. (includes small and large materials): there’s more solutes in the blood
Osmotic Pressure in blood > in interstitial fluid
Arteriole side of capillary bed = net flow out
Venule side of bed = net flow in
85% of fluid leaving arteriole end of capillary reenters at venule end
15% eventually returned by lymphatic system = parallel circulatory system without RBC
low pressure — no O2 content
has valves to prevent backflow
propagated along by contraction of skeletal muscles
will enter back into bloodstream near shoulders
has lymph nodes for immune function to filter and attack bacteria or viruses (WBC)
Movement of Fluid Between Capillaries and Interstitial Fluid
As blood enters capillary (arterial end)
blood pressure is 32 mm Hg (based on hydrostatic pressure: force that blood exerts against a vessel wall)
Osmotic pressure is 22 mm Hg (based on blood proteins/remains constant)
32 mmHg - 22 mmHg = 10 mmHg net pressure moves out
Because materials move out, blood pressure drops to 15 mmHg
15 mmHg - 22 mmHg = -7 mmHg net pressure moves in
This is towards the venous end of capillary as blood moves out
Blood (notes)
connective tissue consisting of…
cells (45%)
liquid matrix called plasma (55%) that suspends cells
Plasma
90% water
electrolytes — inorganic salts (ions), maintains osmotic balance
plasma proteins — escort lipids, antibodies, clotting factors
serum — plasma without clotting factors
nutrients
metabolic wastes
gases
hormones
Cellular Elements
erythrocytes = RBC
no mitochondria to use up O2!
contains 250 × 10^6 molecules of hemoglobin
leukocytes = WBC
include lymphocytes and neutrophils
platelets = cell fragments used in clotting
Cellular Components of Blood
Multipotent Stem Cell in Red Marrow (in bone)
branches into…
Myeloid stem cell
Lymphoid stem cell
Myeloid — innate (first line of defense)
platelets
erythrocytes
basophil
eosinophil
neutrophil
monocyte/macrophage
Lymphoid — adaptive (acquired defense)
Lymphocytes: B and T
Blood Clotting (notes)
Injured blood vessel —> chemicals release
platelets attach by being made to be “sticky”
clotting factors are activated — Prothrombin (inactive) to Thrombin (enzyme)
Thrombin targets fibrinogen (zymogen) peptide linkage which activates it to fibrin
Once activated fibrin is not soluble and precipitates out, it forms a net that holds platelets in place
Clotting occurs with trapped cells
Cardiovascular Diseases (notes)
heart attack = death of heart muscle due to blockage of coronary arteries
blockage prevents certain sections of muscles from getting nutrients it needs —> that part of the muscle dies
stroke = death of neural tissues in brain
could be caused by clogged artery or breakage of artery
heart muscle and neurons not replaceable
Thrombus = clot
Embolus = moving clot
thrombus breaks off and floats until it plugs up stream of capillary beds
Atherosclerosis = plaques in inner walls of arteries
chronic disease
clot that accumulates fatty acids, macrophages, and cholesterol —> cutting down diameter of artery
Arteriosclerosis = plaque hardens by calcium deposits
Fat connection: too much cholesterol ☹
LDL (low density lipoproteins) in blood lead to deposition of fats and cholesterol in plaque
Hypertension (high blood pressure) promotes atherosclerosis
Osmoregulation (notes)
Maintaining homeostasis requires maintaining correct water and salt balance
avoid wide fluctuations in ion conc. and pH
animals can’t survive large fluctuations
too much H2O = cells burst
too much H2O loss = cells shrivel and die
Osmosis: diffusion H2O across semipermeable membrane from high water conc. to low water conc.
hyposmotic = low solute
isosmotic = equal solute
hyperosmotic = high solute
Osmoconfomers (notes)
Animals who evolved in the ocean are considered osmoconformers
Does not adjust internal osmolarity
extracellular fluid/interstitial fluid is isosmotic to ocean water (equal solute conc)
many differ in ion ratios from sea water: ionoregulators and ionoconformers
Ionoconformer = exact same concentration and ratios of ions from surroundings (interstitial fluid is basically sea water)
Ionoregulators = requires energy expenditure for ions to be pumped across membranes against their gradients
Osmoconformers-ionoregulators ECF has the same total ion conc. as sea water
Osmoregulators (notes)
internal ECF not isosmotic to sea water
ALL osmoregulators are ionoregulators
requires energy!
adjusts internal osmolarity by adjusting solute concentration
special transport epithelium required to regulate ion conc., pH, and water conc.
NO PUMPS for water on cell/tissue level
water moved by osmotic gradients
SOME marine, ALL freshwater, and all terrestrial animals
Vertebrates: evolutionary example
Marine vertebrates originally isosmotic (hagfish, lampreys. ancestors of Gnathostomata)
Gnathostomes moved in to FRESH water habitats
I.F. has become hyperosmotic (adapted from salt—>fresh water)
water will actively move into body through skin but mostly through gills
Adaptations:
large amounts of dilute urine (prevents overhydration as water keeps coming in)
uptake of salts to ensure they maintain proper amounts of ions
decrease solute conc. of body fluids (lowers energy expended to maintain homeostasis)
Some groups move back to ocean (SALT water)
I.F. has become hyposmotic
water will actively move out of body
Adaptations:
drinks large amounts of water (balance out water lost)
pumps excess salt out through gills (to balance the increased salt intake from drinking sea water)
small amount of concentrated urine
Salmon gills readapted each time they move from freshwater, salt water, and freshwater again
Metabolic Waste (notes)
Metabolism of proteins and nucleic acids produces nitrogenous wastes
NH3 highly toxic
amino acids have to be deaminated —> collection of NH3 must be rid of because it’s virtually useless
NH3 is very soluble in water
In small animals, simple diffusion gets rid of metabolic waste
In large animals, cells are not in contact with environment
requires special organs to remove waste
Excretion = rids body of waste material INSIDE body
Elimination = rids body of undigested waste that was never in your body in the first place
Excretion of nitrogenous waste evolved secondarily
Aquatic animals usually excrete NH3
Terrestrial animals
to get rid of metabolic waste, salt and water loss always occurs
Some animals combine 2 waste products
Urea = CO2 and NH3 which is less toxic and conserves water
Uric Acid = far less toxic than NH3, low solubility in water (solid waste, less water wasted, more energy required)
Most animals have a combo of Urea, Uric Acid, and NH3 in different amounts
Primary Osmoregulatory Adaptations of Arthropods, Vertebrates, etc., to conserve water
Behavioral Adaptations — thirst, brain pushes you to drink water
Excretory organs conserve water
mostly birds and mammals — hyperosmotic urine
Impervious covering that prevents water loss
Arthropods — waxy layer on exoskeleton, cuticle
Vertebrates — layers of dead keratinized cells
base cells are cuboidal and divide, pushing other cells up which eventually die and accumulate
Organs for osmoregulation/excretory systems
Dependent on transport epithelium
solutes/ion actively pumped
Water follows osmotic gradients
Types:
A. Protonephridia
B. Metanephridia
C. Malpighian tubules
D. Mammalian Kidney
Protonephridia
simplest system
branched system of closed tubes lacking internal openings — only has openings to outside body
tubes of simple cuboidal epithelia
Primarily used for osmoregulation (excretion by simple diffusion across body wall)
Ex. Flatworms (Platyhelminthes)
protonephridia inside body capped by flame bulb cell
cilia beat INSIDE fame bulb to produce pressure to move fluid through tubules
opening on wall of body where urine is excreted
Processes:
Filtration (non selective, except for size) —
nothing can differentiate small molecules: amino acid, salt, nitrogenous waste molecule
Reabsorption (selective, returns to hemolymph) —
requires active transport
pumps move glucose back from urine into hemolymph
Secretion (selective, adds to filtrate) —
materials that are too concentrated in hemolymph, filtering doesn’t work (ex. hydrogen ions)
actively transported across protonephridia
Initial fluid is hemolymph but just the small particles which moves through the protonephridia where it is chemically changed by reabsorption and secretion so that when it reaches the opening, what comes out is the finished, hypsomotic urine
Metanephridia
Slightly more complex than protonephridia
in annelids, Oligochaeta — right and left metanephridia on each segment
Openings both on inside of body and body wall
Nephrostome — opening into interstitial fluid
in one segment, it’s surrounded by capillary beds
second segment purifies I.F. in preceding segment
Has some filtration, reabsorption of salts and other metabolites, and secretion
Hyposmotic dilute urine + nitrogenous waste handled (unlike in protonephridia)
Nephridiopore — opening to outside
one on each side of each segment
Malpighian Tubules
In insects
Filters hemolymph
Blind tubes connected to junction between midgut and hindgut
Driving force is H+ ATPase in apical membrane of epithelium
Malpighian Tubule Secretion
H+ ATPase (apical): pumps H+ into lumen of tube
HIGH [H+] in lumen, LOW [H+] in cell
H+/K+ cotransporter (apical): protons naturally follow gradient back INSIDE cell, meanwhile co-transporting K+ OUT of cell and into lumen
HIGH [K+] in lumen, LOW [K+] in cell
Chlorine Channel: Chlorine follows and neutralizes positive charge
K+/Na+/2Cl- cotransporter (basal): moves 1 K+, 2 Cl-, 1 Na+ into lumen
balanced charges
driving force is K+ gradient, naturally moves into cell
2 Cl- and Na+ move through channels into lumen
As this occurs, water moves through aquaporins (pores for water)
Water follows salts, as it moves into lumen, other nutrients may flow in too (bulk flow)
Water can only move DOWN tube into gut
Some stuff can be reabsorbed in proximal tubule
amino acids, sugars
Primary urine enters midgut — rich in K+, Na+, Cl-
Water and salts reabsorbed in rectum
Malpighian Tubules Reabsorption in Hind Gut
Cl- ATPase (apical) — creates low conc. of Cl- inside lumen, high conc. of Cl- inside cell
Chlorine Channel (basal)— facilitates movement of Cl- from inside cell to hemolymph
Na+/K+ ATPase (basal) — 3 Na+ pumped out to hemolymph and 2 K+ pumped in
creates low Na+ concentration in cell
Sodium Channel (apical) — facilitates movement of High [Na+] in lumen to Low [Na+] in cell
As Na, K, and Cl moves, water moves down gradient into cell
Water gets removed from lumen/gut, waste becomes more concentrated
Uric acid precipitates
K+ channels (apical and basal) — maintains balance as other ions move?
Mammalian Kidneys
Compact organ with excretory tubes
For excretion and osmoregulation (major organ for balancing pH)
Blood goes into renal artery —> kidneys (where blood is filtered) —> renal vein —> vena cava
Filtered waste goes from kidneys —> ureter —> bladder —> urethra —> urine
Structure: 2 major layers
outer cortex
inner medulla
contains nephrons (filtering unit?) and collecting ducts (simple cuboidal epithelium)
Nephron
Bowman’s Capsule (simple squamous) empties into proximal tubule
It makes two sharp turns forming the Loop of Henle — proximal tubule descends down into medulla and then ascends up into distal tubule
Distal tubule connects to collecting duct that goes deep into medulla —> renal pelvis —> ureter —> bladder
Kidney Blood Supply into Nephron
Afferent arteriole —> Glomerulus (bowman’s capsule capillary beds) —> Efferent arteriole —> Peritubular Capillaries (capillary beds that surround proximal and distal tubules) —> Vasa Recta (net of capillary beds that surround Loop of Henle) —> venule —> renal vein
Loop of Henle and Vasa Recta run counter current to each other