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Unit 2
Renal Physiology
Objectives
Unit #2-Lecture 2
Lecture Objectives: Upon completion of this class material each student will be able to do the
following:
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Renal Physiology
Unit 2b
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2. Excrete urine (micturition)
II. Kidney
The functional unit is the nephron. There are approximately 2-2.5 million nephrons
combined in both kidneys, but we only need a portion for our kidney to function. All
nephrons start in the cortex of the kidney.
A. Types of Nephrons
1. Cortical
These are short and represent approximately 85% of all nephrons. Most of
this nephron is located in the cortex, but the bottom of the loop of henle is
located in the medulla.
2. Juxtamedullary
These are long and represent approximately 15% of all nephrons. The
bowman’s capsule is in the cortex, but the entire loop of henle is in the
medulla.
B. Juxtaglomerular Apparatus
This apparatus is one component of an important feedback mechanism
(tubuloglomerular feedback mechanism) that is involved in the autoregulation of `
renal blood flow and glomerular filtration rate (GFR).
The macula densa cells contact the EGM and the granular cells of the afferent and
efferent arterioles when they sense any type of change. The granular cells are
modified smooth muscle cells that manufacture, store and release renin. Renin is
involved in the formation of angiotensin II and ultimately in the secretion of
aldosterone.
Example
BP, GFR, Cl reabsorption
These decreases, especially Cl, are detected by the Macula Densa cells of
the Juxtaglomerular apparatus. The Macula Densa will release
prostaglandins that will stimulate the Granular Cells of the afferent and
efferent to release renin into the blood and this converts Angiotensinogen
to Angiotensin I. Angiotensin I is converted to Angiotensin II by and
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enzyme called Angiotensin Conversion Enzyme. Angiotensin II is a very
potent vasoconstrictor, which will lead to systemic vasoconstriction. This
will increase BP, GFR and Cl reabsorption. These increases will cause
renin to stop being released by the Granular cells.
V. Production of Urine
A. Primary Urine
Urine that is filtered by the glomerulus through the glomerular filter, which has
the layers:
Endothelial cells
Basement membrane
Slit pores of podocytes
The filtrate that is allowed to enter the nephron is Na, K, Cl, Ca, water, glucose
and proteins with a molecular weight of <20,000 daltons to pass. In order for
filtration to occur two factors must be met:
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1. Hydrostatic pressure at the end of the afferent arteriole is 45 mmHg.
The hydrostatic pressure in the bowman’s capsule is 10 mmHg. The
driving force is the difference in hydrostatic pressure.
2. The osmotic pressure of blood is 25 mmHg and the osmotic pressure
in the bowman’s capsule and interstitial fluid is 0 mmHg.
**The actual driving force of glomerular filtration is the difference between
hydrostatic pressure and osmotic pressure, this is called the Starling Hypothesis.
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move on to the collecting part of the DCT which removes Na and Cl from the
lumen back into the body. Now since we have removed all these molecules: Na,
K, Cl, Ca, etc. The urine is now more hypotonic or less concentrated and ready to
be excreted.
F. Bladder
The urine in the bladder is detected by the stretch receptors because of transitional
epithelium found in the urinary bladder and sends a signal to the sympathetic
nervous system of the spinal cord saying the bladder is full or almost full. This
signal may be overridden by the parasympathetic nervous system.
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reabsorbed into the body. This causes the urine volume to decrease. ADH is associated
with the disease state Diabetes insipidus.