Hyponatremia pathophysiology: Difference between revisions
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‡ <small>''Mmol and Meq are the same for univalent ions like sodium, potassium, for Na<sup>+</sup>, Cl<sup>-</sup>, Ca<sup>2+</sup>, urea, and glucose, 1 mmol/L equals 1 mOsmol/kg''</small> | ‡ <small>''Mmol and Meq are the same for univalent ions like sodium, potassium, for Na<sup>+</sup>, Cl<sup>-</sup>, Ca<sup>2+</sup>, urea, and glucose, 1 mmol/L equals 1 mOsmol/kg''</small> | ||
Plasma water is regulated by sensory organs (baroreceptors and hypothalamus osmoreceptors), antidiuretic hormone (ADH or vasopressin), and the kidney | Plasma water is regulated by sensory organs (baroreceptors and hypothalamus osmoreceptors), antidiuretic hormone (ADH or vasopressin), and the kidney. | ||
Osmoreceptors in the hypothalamus are sensitive to the increased tonicity of serum, cause increase secretion of ADH from posterior pituitary. '''ADH secretion from hypothalamus through posterior pituitary is increased by <ref>{{Cite journal | Osmoreceptors in the hypothalamus are sensitive to the increased tonicity of serum, cause increase secretion of ADH from posterior pituitary. '''ADH secretion from hypothalamus through posterior pituitary is increased by <ref>{{Cite journal | ||
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* ↓ Baroreceptor firing ( ↓effective intravascular volume) | * ↓ Baroreceptor firing ( ↓effective intravascular volume) | ||
* ↓ Right atrium stretching | * ↓ Right atrium stretching | ||
ADH increases renal free water reabsorption from the collecting tubules and results in correction of plasma sodium toward the normal range. The vasopressin type 2 (V<sub>2</sub>) receptor in the basolateral membrane of the collecting tubule acts as antidiuretic effect of ADH. Binding of ADH to V2 receptor <ref name="HolmesLandry2003">{{cite journal|last1=Holmes|first1=Cheryl L|last2=Landry|first2=Donald W|last3=Granton|first3=John T|journal=Critical Care|volume=7|issue=6|year=2003|pages=427|issn=13648535|doi=10.1186/cc2337}}</ref> intensifies action of intracellular cyclic adenosine monophosphate (cAMP) and results in insertion of water channel (aquaporin 2) into the luminal membrane and increasing in the number of aquaporin 2 mRNA level <ref name="KwonHager2001">{{cite journal|last1=Kwon|first1=Tae-Hwan|last2=Hager|first2=Henrik|last3=Nejsum|first3=Lene N.|last4=Andersen|first4=Marie-Louise E.|last5=Fr[oslash]ki[aelig ]r|first5=J[oslash]rgen|last6=Nielsen|first6=S[oslash]ren|title=Physiology and pathophysiology of renal aquaporins|journal=Seminars in Nephrology|volume=21|issue=3|year=2001|pages=231–238|issn=02709295|doi=10.1053/snep.2001.21647}}</ref>.As plasma water increases, plasma sodium concentration, osmolality, and ADH secretion decrease and the collecting tubule becomes impermeable to water, leads to excretion of free water and restoration of the plasma sodium concentration.[[File:ADH-mechanism of action-1.JPG|thumb|750px|center| Mechanism of action of ADH , (ɔ) Image courtesy of WikiDoc.org, by '''"[[User:Saeedeh Kowsarnia|Dr. Saeedeh Kowsarnia]]"''']]'''Renin-Angiotensin-Aldosteron System:'''[[File:RAAS.jpg|center|thumb|Renin-Angiotensin-Aldosteron System.Source- Wikimedia <ref>By Soupvector - Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=66583851</ref>]] | ADH increases renal free water reabsorption from the collecting tubules and results in correction of plasma sodium toward the normal range. The vasopressin type 2 (V<sub>2</sub>) receptor in the basolateral membrane of the collecting tubule acts as antidiuretic effect of ADH. Binding of ADH to V2 receptor <ref name="HolmesLandry2003">{{cite journal|last1=Holmes|first1=Cheryl L|last2=Landry|first2=Donald W|last3=Granton|first3=John T|journal=Critical Care|volume=7|issue=6|year=2003|pages=427|issn=13648535|doi=10.1186/cc2337}}</ref> intensifies action of intracellular cyclic adenosine monophosphate (cAMP) and results in insertion of water channel (aquaporin 2) into the luminal membrane and increasing in the number of aquaporin 2 mRNA level <ref name="KwonHager2001">{{cite journal|last1=Kwon|first1=Tae-Hwan|last2=Hager|first2=Henrik|last3=Nejsum|first3=Lene N.|last4=Andersen|first4=Marie-Louise E.|last5=Fr[oslash]ki[aelig ]r|first5=J[oslash]rgen|last6=Nielsen|first6=S[oslash]ren|title=Physiology and pathophysiology of renal aquaporins|journal=Seminars in Nephrology|volume=21|issue=3|year=2001|pages=231–238|issn=02709295|doi=10.1053/snep.2001.21647}}</ref>.As plasma water increases, plasma sodium concentration, osmolality, and ADH secretion decrease and the collecting tubule becomes impermeable to water, leads to excretion of free water and restoration of the plasma sodium concentration.[[File:ADH-mechanism of action-1.JPG|thumb|750px|center| Mechanism of action of ADH , (ɔ) Image courtesy of WikiDoc.org, by '''"[[User:Saeedeh Kowsarnia|Dr. Saeedeh Kowsarnia]]"''']]Hyponatremia is defined as serum sodium less than 135 mEq/L (mmol/L).Hyponatremia is a water balance disorder which represents an imbalance in a ratio where total body water is more than total body solutes( total body sodium and total body potassium). | ||
'''Renin-Angiotensin-Aldosteron System:'''[[File:RAAS.jpg|center|thumb|Renin-Angiotensin-Aldosteron System.Source- Wikimedia <ref>By Soupvector - Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=66583851</ref>]] | |||
Hyponatremia represents as an excess of water relative to total body sodium, resulting from impaired water excretion by the kidneys or the depletion of sodium in excess of water. | Hyponatremia represents as an excess of water relative to total body sodium, resulting from impaired water excretion by the kidneys or the depletion of sodium in excess of water. | ||
Revision as of 15:59, 25 April 2018
Hyponatremia Microchapters |
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Hyponatremia pathophysiology On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Saeedeh Kowsarnia M.D.[2]
Overview
The exact pathogenesis of [disease name] is not fully understood.
OR
It is thought that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3]
OR
[Pathogen name] is usually transmitted via the [transmission route] route to the human host.
OR
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
OR
Blo [Disease or malignancy nme] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
OR
The progression to [disease name] usually involves the [molecular pathway].
OR
The pathophysiology of [disease/malignancy] depends on the histological subtype.
Pathophysiology
Sodium is the main cation in the extracellular fluid, thus the plasma concentration of sodium is determinant of tonicity and serum osmolality.
The osmotic gradient of solutes that do not cross cell membranes constitutes serum Tonicity [1] which determines the distribution of water in the body.
Plasma tonicity = (Extracellular solute + Intracellular solute) / TBW
Serum or plasma osmolality measures different solutes in plasma. It helps to evaluate the etiology of hyponatremia and screen other solutes in serum.
Serum Osmolality = (2 x (Na + K)) + (BUN (mg/dL) / 2.8) + (glucose (mg/dL) / 18) + (Ethanol (mg/dL) /3.7) [2]
Normal Range= 275–295 mosm /kg (mmol /kg)
Normal range | Osmolality versus Osmolarity | |
---|---|---|
Sodium‡ | 135-145 mEq/L |
(one liter of plasma equals to one kilogram of plasma,plasma osmolarity and plasma osmolality would be the same) |
Potassium‡ | 3.5-5.1 mEq/L | |
Blood Urea Nitrogen | 7-20 mg/dL (2.5-7.1 mmol/L) | |
Glucose | 70-100 mg/dL ( 3.9-5.5 mmol/L) |
‡ Mmol and Meq are the same for univalent ions like sodium, potassium, for Na+, Cl-, Ca2+, urea, and glucose, 1 mmol/L equals 1 mOsmol/kg
Plasma water is regulated by sensory organs (baroreceptors and hypothalamus osmoreceptors), antidiuretic hormone (ADH or vasopressin), and the kidney.
Osmoreceptors in the hypothalamus are sensitive to the increased tonicity of serum, cause increase secretion of ADH from posterior pituitary. ADH secretion from hypothalamus through posterior pituitary is increased by [4] [5]:
- ↑ Angiotensin II (activation of Renin-Angiotensin-Activation System)
- ↑ Sympathetic stimulation
- ↑ Effective osmoles (Hypertonicity)
- ↓ Baroreceptor firing ( ↓effective intravascular volume)
- ↓ Right atrium stretching
ADH increases renal free water reabsorption from the collecting tubules and results in correction of plasma sodium toward the normal range. The vasopressin type 2 (V2) receptor in the basolateral membrane of the collecting tubule acts as antidiuretic effect of ADH. Binding of ADH to V2 receptor [6] intensifies action of intracellular cyclic adenosine monophosphate (cAMP) and results in insertion of water channel (aquaporin 2) into the luminal membrane and increasing in the number of aquaporin 2 mRNA level [7].As plasma water increases, plasma sodium concentration, osmolality, and ADH secretion decrease and the collecting tubule becomes impermeable to water, leads to excretion of free water and restoration of the plasma sodium concentration.
Hyponatremia is defined as serum sodium less than 135 mEq/L (mmol/L).Hyponatremia is a water balance disorder which represents an imbalance in a ratio where total body water is more than total body solutes( total body sodium and total body potassium). Renin-Angiotensin-Aldosteron System:
Hyponatremia represents as an excess of water relative to total body sodium, resulting from impaired water excretion by the kidneys or the depletion of sodium in excess of water.
Hypotonic (dilutional) hyponatraemia is classified by the extracellular volume status into hypo-, eu- and hyper-volemic hyponatremia.
Term | Definitions[9][10][11] |
---|---|
Hyponatremia | Hyponatremia is defined as a serum sodium concentration < 135 mEq/L. |
Hypotonic hyponatremia | Hyponatremia with low osmolality (hypotonic hyponatremia) is defined as hyponatremia with a serum osmolality below 280 mOsm/kg. |
Hypertonic hyponatremia | Hyponatremia with high osmolality (hypertonic hyponatremia) is defined as hyponatremia with a serum osmolality greater than 295 mOsm/kg. |
Isotonic hyponatremia | Hyponatremia with normal osmolality (Isotonic hyponatremia) is defined as hyponatremia with a serum osmolality ranging between 280-295 mOsm/kg. |
Hyponatremia based on ECF volume | |
Hypovolemic hyponatremia | Hyponatremia plus decreased extracellular cellular fluid volume. Usually diagnosed by history and physical examinationshowing water depletion plus spot urine sodium <20 to 30 mmol/L, unless kidney is the source of sodium loss. |
Euvolemic hyponatremia | Hyponatremia plus normal extracellular cellular fluid volume. Majority of cases are of this type. Usually diagnosed by spot urine sodium ≥ 20 to 30 mmol/L, unless secondarily sodium depleted. |
Hypervolemia hyponatremia | Hyponatremia plus increased extracellular cellular fluid volume. Usually diagnosed by history and physical examinationshowing water retention plus spot urine sodium <20 to 30 mmol/L |
Pathogenesis
- The exact pathogenesis of [disease name] is not fully understood.
OR
- It is understood that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
- [Pathogen name] is usually transmitted via the [transmission route] route to the human host.
- Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
- [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
- The progression to [disease name] usually involves the [molecular pathway].
- The pathophysiology of [disease/malignancy] depends on the histological subtype.
Genetics
- [Disease name] is transmitted in [mode of genetic transmission] pattern.
- Genes involved in the pathogenesis of [disease name] include [gene1], [gene2], and [gene3].
- The development of [disease name] is the result of multiple genetic mutations.
Associated Conditions
Gross Pathology
- On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Microscopic Pathology
- On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
References
- ↑ Sperelakis, Nick (2012). Cell physiology sourcebook : essentials of membrane biophysics. London, UK Waltham, MA, USA: Elsevier/Academic Press. ISBN 978-0-12-387738-3.
- ↑ Purssell, Roy A.; Pudek, Morris; Brubacher, Jeffrey; Abu-Laban, Riyad B. (2001). "Derivation and validation of a formula to calculate the contribution of ethanol to the osmolal gap". Annals of Emergency Medicine. 38 (6): 653–659. doi:10.1067/mem.2001.119455. ISSN 0196-0644.
- ↑ Erstad BL (2003). "Osmolality and osmolarity: narrowing the terminology gap". Pharmacotherapy. 23 (9): 1085–6. PMID 14524639.
- ↑ G. L. Robertson (1987). "Physiology of ADH secretion". Kidney international. Supplement. 21: S20–S26. PMID 3476800. Unknown parameter
|month=
ignored (help) - ↑ L. Share (1967). "Vasopressin, its bioassay and the physiological control of its release". The American journal of medicine. 42 (5): 701–712. PMID 5337374. Unknown parameter
|month=
ignored (help) - ↑ Holmes, Cheryl L; Landry, Donald W; Granton, John T (2003). Critical Care. 7 (6): 427. doi:10.1186/cc2337. ISSN 1364-8535. Missing or empty
|title=
(help) - ↑ Kwon, Tae-Hwan; Hager, Henrik; Nejsum, Lene N.; Andersen, Marie-Louise E.; Fr[oslash]ki[aelig ]r, J[oslash]rgen; Nielsen, S[oslash]ren (2001). "Physiology and pathophysiology of renal aquaporins". Seminars in Nephrology. 21 (3): 231–238. doi:10.1053/snep.2001.21647. ISSN 0270-9295.
- ↑ By Soupvector - Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=66583851
- ↑ Laczi, F. (2008). "[Etiology, diagnostics and therapy of hyponatremias]". Orv Hetil. 149 (29): 1347–54. doi:10.1556/OH.2008.28409. PMID 18617466. Unknown parameter
|month=
ignored (help) - ↑ Douglas, I. (2006). "Hyponatremia: why it matters, how it presents, how we can manage it". Cleve Clin J Med. 73 Suppl 3: S4–12. PMID 16970147. Unknown parameter
|month=
ignored (help) - ↑ Verbalis, JG.; Goldsmith, SR.; Greenberg, A.; Korzelius, C.; Schrier, RW.; Sterns, RH.; Thompson, CJ. (2013). "Diagnosis, evaluation, and treatment of hyponatremia: expert panel recommendations". Am J Med. 126 (10 Suppl 1): S1–42. doi:10.1016/j.amjmed.2013.07.006. PMID 24074529. Unknown parameter
|month=
ignored (help)