Endocrinology
|
April 10, 2024

ADH Hormone: Understanding Its Role in Body's Fluid Balance

Medically Reviewed by
Updated On
September 17, 2024

Antidiuretic Hormone (ADH), also known as arginine vasopressin (AVP) or vasopressin, is a vital hormone responsible for regulating water balance in the body. ADH is produced in the hypothalamus of the brain and travels throughout the body via the blood. Through its impact on the kidney’s ability to reabsorb water, ADH plays a critical role in maintaining proper hydration levels and overall osmotic balance within the body.

This article aims to explore the functions of ADH, how this hormone impacts health, and its significance in maintaining physiological equilibrium. By understanding the intricate mechanisms through which ADH regulates water balance in the body you can understand its essential role in health and balance.

[signup]

What is ADH Hormone?

ADH’s roles in regulating water balance in the body make it a key player in the control of the body’s osmotic balance, blood pressure regulation, sodium homeostasis, and kidney functioning. This vasopressin hormone also has wide-reaching impacts on reproduction, complex behavior, memory, and learning.Β 

ADH is synthesized by neurons that have their cell bodies within the supraoptic and paraventricular nuclei of the hypothalamus, a region of the brain that is responsible for controlling various physiological processes. These neurons project into the pituitary gland and terminate on groups of capillary blood vessels scattered throughout the posterior pituitary. These blood vessels drain into the systemic circulation via the cavernous sinus and superior vena cava, allowing ADH to travel throughout the body in the bloodstream and act on target tissues.

Osmolality is a measure of the concentration of dissolved particles in your blood and other body fluids like urine. Osmolality is impacted by the levels of water and the concentration of chemicals like chloride, sodium, proteins, bicarbonate, and glucose in your blood.Β 

When osmoreceptors in the hypothalamus detect changes in the body’s balance, such as increased plasma osmolality or decreased blood volume, ADH is released. In addition, there are baroreceptors in the heart and blood vessels that help to detect changes in blood pressure and blood volume, which then stimulates ADH to be released and signals water reabsorption in the kidneys. This helps to keep blood pressure and blood volume at a stable level.

The Mechanism of ADH Action

Here's how ADH functions in the body:

ADH and Water Reabsorption

One of the main targets of ADH is the kidney. ADH binds to receptors on the cells lining the renal tubules and collecting ducts of the kidneys. When ADH binds to these vasopressin receptors (V1 and V2 receptors), it activates intracellular signaling pathways that lead to the insertion of water channel proteins (aquaporins) in the cell membrane.Β 

These aquaporin channels make the renal tubules and collecting ducts more permeable to water, allowing water to move across the cell membrane. This reduces water lost in the urine and increases water reabsorption back into the blood. As a result, the urine becomes more concentrated and of a lower volume to help prevent dehydration. This mechanism helps the body conserve water when plasma osmolality becomes too concentrated or the body is dehydrated.Β Β 

ADH Response to Body's Needs

The release of ADH is regulated by the hypothalamus in response to detecting the body’s needs. ADH secretion is primarily triggered by increases in the levels of solutes in the blood (osmolality) and decreases in blood volume (dehydration). Feedback mechanisms help to ensure that ADH secretion is adjusted appropriately to maintain fluid balance and prevent dehydration or overhydration.

When there is a higher concentration of solutes such as chloride, sodium, proteins, bicarbonate, and glucose in the blood, osmoreceptors in the hypothalamus of the brain sense this elevated plasma osmolality. Once the concentration of solutes reaches a threshold level, these osmoreceptors trigger the release of ADH from the posterior pituitary gland. This hormone travels through the bloodstream to act on the kidneys, causing an increase in water reabsorption to reduce plasma osmolality and restore fluid balance.

In addition, baroreceptors located in the heart and blood vessels can also stimulate ADH release when they sense decreased blood volume and blood pressure. This can occur due to dehydration, increased blood loss, or other medical conditions

Other triggers for ADH release include pain, stress, nausea, and certain medications like nicotine and opiates that act indirectly through the activation of the hypothalamic-pituitary-adrenal (HPA) axis or other neural pathways. ADH secretion can also be impacted by changes in physical activity or temperature.Β 

As ADH acts on the kidneys to increase water reabsorption, negative feedback mechanisms are activated to help regulate its further secretion to prevent overcorrection. Once plasma osmolality decreases to normal levels, blood volume increases, and blood pressure rises, the osmoreceptors in the hypothalamus inhibit further ADH release, and baroreceptors signal the hypothalamus to reduce ADH secretion.

Health Implications of ADH

ADH plays an important role in our health.

The Role of ADH in Blood Pressure Regulation

In addition to regulating water reabsorption in the kidney, ADH has secondary effects on the blood vessels, influencing vascular tone and blood pressure via vasoconstriction. ADH causes constriction of vascular smooth muscle cells and vasoconstriction by binding to vasopressin receptors (V1 receptors). ADH-induced vasoconstriction helps to maintain blood pressure and tissue perfusion, especially under conditions of significant fluid loss or low blood volume.

These actions of ADH on the blood vessels work to complement the impacts of the renin-angiotensin-aldosterone system (RAAS). This helps the body regulate vasoconstriction and maintain blood pressure.

Disorders Associated with ADH Imbalance

Abnormal levels of ADH can lead to clinical conditions, including diabetes insipidus (DI) and Syndrome of Inappropriate Antidiuretic Hormone secretion (SIADH). These conditions have significant impacts on fluid and electrolyte balance.

Diabetes insipidus occurs when there is inadequate production or secretion of ADH and/or renal insensitivity to ADH. This causes excessive urine output (polyuria) and frequent urination at night (nocturia) which can result in dehydration, electrolyte imbalances, and excessive thirst (polydipsia).

Central DI results from a deficiency in ADH secretion from the brain due to trauma, tumors, infections, or genetic factors that impact the functioning of the hypothalamus or posterior pituitary gland. If the kidneys do not respond appropriately to ADH, causing impaired water reabsorption in the renal tubules, nephrogenic DI results. This can occur due to genetic mutations in the vasopressin receptors, from kidney disease, or due to certain medications, such as lithium and tetracycline.

SIADH occurs when there is too much secretion of ADH despite normal or low plasma osmolality. This causes impaired water excretion, low sodium (dilutional hyponatremia), fluid retention, and concentrated urine with high osmolality despite low plasma osmolality. Tumors, trauma, or infections in the brain; pulmonary disorders such as pneumonia or small cell lung cancer; and certain medications including selective serotonin reuptake inhibitors can cause SIADH.Β 

Diagnosing and Treating ADH-Related Disorders

Diagnosing and treating ADH-related disorders doesn't have to be complicated. See below to learn how:

Diagnostic Tests for ADH Imbalance

ADH function and related imbalances are evaluated using a combination of clinical evaluation, laboratory tests, and imaging studies.Β 

A thorough medical history and physical examination help to identify symptoms and signs that suggest imbalances in ADH. These can include increased thirst (polydipsia), increased urination (polyuria), increased nighttime urination (nocturia), dehydration, or fluid retention.

Urine and blood testing can help assess ADH levels as well as fluid and electrolyte imbalances. For example, serum osmolality measures the concentration of solutes in the blood. If serum osmolality is low, it can suggest SIADH, while high serum osmolality may indicate dehydration or diabetes insipidus.

Urinary osmolality is valuable for assessing the kidney's ability to concentrate or dilute urine.

Urinary osmolality is typically low in DI despite high serum osmolality, indicating that the kidneys are not properly concentrating urine. On the other hand, with SIADH, urinary osmolality is typically elevated despite low serum osmolality since the kidneys are retaining excess water.

Measuring sodium levels in the blood can also help assess ADH function. If levels of sodium are low in the blood (hyponatremia) it can suggest SIADH due to dilutional effects from water retention. If excess water is being lost in DI, sodium levels in the blood can be elevated.Β 

ADH or copeptin can also be measured in plasma or serum to directly evaluate ADH secretion. Low levels of ADH suggest central DI, while high or inappropriately normal ADH levels suggest SIADH. ADH levels can also be measured after giving a bolus of hypertonic saline or after restricting water intake to assess ADH secretion under different conditions. During a fluid deprivation test, urine osmolality and serum sodium are repeatedly measured to monitor changes in hydration status and resulting ADH release. If the urine fails to concentrate despite dehydration, this suggests impaired ADH secretion such as occurs with central DI. If the urine concentration increases significantly, this indicates that ADH secretion is intact and the issue is likely to be nephrogenic DI or SIADH.

In some cases, neuroimaging studies, such as magnetic resonance imaging (MRI) or computed tomography (CT) scans, may be needed to evaluate the hypothalamus, pituitary gland, and/or surrounding structures for abnormalities, tumors, or lesions that may be causing or contributing to ADH-related disorders.

Evaluate for potential underlying causes, including head trauma, brain tumors, infections, medications, or other medical conditions that may affect ADH secretion or responsiveness.

Treatment Options

The treatment of ADH-related disorders depends on the specific cause and resulting symptoms. Diabetes insipidus is typically treated by replacing ADH using synthetic analogs (desmopressin). This helps to correct the fluid and electrolyte imbalances. In addition, any identified underlying causes should be addressed when possible.Β 

SIADH is treated by identifying and managing the underlying cause. Fluid intake is restricted to prevent further fluid overload. In some cases, hypertonic saline or demeclocycline may be given to increase free water excretion.

Lifestyle and ADH Regulation

Incorporating specific lifestyle recommendations can also be helpful.

Hydration and ADH

Maintaining proper hydration is important for balanced ADH levels and overall health. Your individual hydration needs may vary based on many factors, such as climate, activity levels, and medical conditions, so work with a nutritionist or health professional to determine your individual needs.

  • Overall, to maintain adequate hydration it is important to listen to your body. Pay attention to signs of dehydration like thirst, dry mouth, fatigue, dizziness, dark-colored urine, or reduced urine output.Β 
  • Drink water with electrolytes like sea salt or coconut water when you are thirsty and aim for a pale yellow urine color.Β 
  • In general, around 3.7 liters (125 ounces) per day for men and 2.7 liters (91 ounces) for women provide adequate hydration. This can come from beverages and water-rich foods like fruits (e.g., watermelon, oranges, strawberries), vegetables (e.g., cucumber, lettuce, celery), and soups.Β 
  • When you are physically active or the weather is hotter, you may need to drink more water and be sure to balance electrolytes that are lost through sweating.Β 

Impact of Alcohol and Caffeine

Caffeinated beverages and alcohol can increase urine output, so they should be limited and always balanced with water intake.Β 

Caffeine, in coffee, tea, soda, and energy drinks, increases urine production and inhibits the action of ADH, making it less effective at promoting water reabsorption in the kidneys.Β 

Alcohol can also contribute to dehydration by impacting ADH. Alcohol inhibits ADH secretion from the pituitary gland, resulting in increased urine production and dehydration. In addition, alcohol can contribute to dehydration and electrolyte imbalances by inhibiting the reabsorption of water and electrolytes in the kidneys, exacerbating fluid loss.

[signup]

Key Takeaways

ADH serves as a pivotal regulator of water balance and plays a crucial role in maintaining homeostasis within the body. This hormone is produced in the hypothalamus and released from the posterior pituitary gland into the bloodstream in response to low blood volume or increased concentration of dissolved electrolytes and other osmolytes in the blood.Β 

In the kidneys, ADH increases the permeability of the renal tubules and collecting ducts to water. This causes more water to be reabsorbed to maintain water balance and overall homeostasis within the body.

Antidiuretic Hormone (ADH), also known as arginine vasopressin (AVP) or vasopressin, is a vital hormone responsible for regulating water balance in the body. ADH is produced in the hypothalamus of the brain and travels throughout the body via the blood. Through its impact on the kidney’s ability to reabsorb water, ADH plays a critical role in maintaining proper hydration levels and overall osmotic balance within the body.

This article aims to explore the functions of ADH, how this hormone impacts health, and its significance in maintaining physiological equilibrium. By understanding the intricate mechanisms through which ADH regulates water balance in the body, you can understand its essential role in health and balance.

[signup]

What is ADH Hormone?

ADH’s roles in regulating water balance in the body make it a key player in the control of the body’s osmotic balance, blood pressure regulation, sodium homeostasis, and kidney functioning. This vasopressin hormone also has wide-reaching impacts on reproduction, complex behavior, memory, and learning.Β 

ADH is synthesized by neurons that have their cell bodies within the supraoptic and paraventricular nuclei of the hypothalamus, a region of the brain that is responsible for controlling various physiological processes. These neurons project into the pituitary gland and terminate on groups of capillary blood vessels scattered throughout the posterior pituitary. These blood vessels drain into the systemic circulation via the cavernous sinus and superior vena cava, allowing ADH to travel throughout the body in the bloodstream and act on target tissues.

Osmolality is a measure of the concentration of dissolved particles in your blood and other body fluids like urine. Osmolality is impacted by the levels of water and the concentration of chemicals like chloride, sodium, proteins, bicarbonate, and glucose in your blood.Β 

When osmoreceptors in the hypothalamus detect changes in the body’s balance, such as increased plasma osmolality or decreased blood volume, ADH is released. In addition, there are baroreceptors in the heart and blood vessels that help to detect changes in blood pressure and blood volume, which then stimulates ADH to be released and signals water reabsorption in the kidneys. This helps to keep blood pressure and blood volume at a stable level.

The Mechanism of ADH Action

Here's how ADH functions in the body:

ADH and Water Reabsorption

One of the main targets of ADH is the kidney. ADH binds to receptors on the cells lining the renal tubules and collecting ducts of the kidneys. When ADH binds to these vasopressin receptors (V1 and V2 receptors), it activates intracellular signaling pathways that lead to the insertion of water channel proteins (aquaporins) in the cell membrane.Β 

These aquaporin channels make the renal tubules and collecting ducts more permeable to water, allowing water to move across the cell membrane. This reduces water lost in the urine and increases water reabsorption back into the blood. As a result, the urine becomes more concentrated and of a lower volume to help prevent dehydration. This mechanism helps the body conserve water when plasma osmolality becomes too concentrated or the body is dehydrated.Β Β 

ADH Response to Body's Needs

The release of ADH is regulated by the hypothalamus in response to detecting the body’s needs. ADH secretion is primarily triggered by increases in the levels of solutes in the blood (osmolality) and decreases in blood volume (dehydration). Feedback mechanisms help to ensure that ADH secretion is adjusted appropriately to maintain fluid balance and prevent dehydration or overhydration.

When there is a higher concentration of solutes such as chloride, sodium, proteins, bicarbonate, and glucose in the blood, osmoreceptors in the hypothalamus of the brain sense this elevated plasma osmolality. Once the concentration of solutes reaches a threshold level, these osmoreceptors trigger the release of ADH from the posterior pituitary gland. This hormone travels through the bloodstream to act on the kidneys, causing an increase in water reabsorption to reduce plasma osmolality and restore fluid balance.

In addition, baroreceptors located in the heart and blood vessels can also stimulate ADH release when they sense decreased blood volume and blood pressure. This can occur due to dehydration, increased blood loss, or other medical conditions

Other triggers for ADH release include pain, stress, nausea, and certain medications like nicotine and opiates that act indirectly through the activation of the hypothalamic-pituitary-adrenal (HPA) axis or other neural pathways. ADH secretion can also be impacted by changes in physical activity or temperature.Β 

As ADH acts on the kidneys to increase water reabsorption, negative feedback mechanisms are activated to help regulate its further secretion to prevent overcorrection. Once plasma osmolality decreases to normal levels, blood volume increases, and blood pressure rises, the osmoreceptors in the hypothalamus inhibit further ADH release, and baroreceptors signal the hypothalamus to reduce ADH secretion.

Health Implications of ADH

ADH plays an important role in our health.

The Role of ADH in Blood Pressure Regulation

In addition to regulating water reabsorption in the kidney, ADH has secondary effects on the blood vessels, influencing vascular tone and blood pressure via vasoconstriction. ADH causes constriction of vascular smooth muscle cells and vasoconstriction by binding to vasopressin receptors (V1 receptors). ADH-induced vasoconstriction helps to maintain blood pressure and tissue perfusion, especially under conditions of significant fluid loss or low blood volume.

These actions of ADH on the blood vessels work to complement the impacts of the renin-angiotensin-aldosterone system (RAAS). This helps the body regulate vasoconstriction and maintain blood pressure.

Disorders Associated with ADH Imbalance

Abnormal levels of ADH can lead to clinical conditions, including diabetes insipidus (DI) and Syndrome of Inappropriate Antidiuretic Hormone secretion (SIADH). These conditions have significant impacts on fluid and electrolyte balance.

Diabetes insipidus occurs when there is inadequate production or secretion of ADH and/or renal insensitivity to ADH. This causes excessive urine output (polyuria) and frequent urination at night (nocturia) which can result in dehydration, electrolyte imbalances, and excessive thirst (polydipsia).

Central DI results from a deficiency in ADH secretion from the brain due to trauma, tumors, infections, or genetic factors that impact the functioning of the hypothalamus or posterior pituitary gland. If the kidneys do not respond appropriately to ADH, causing impaired water reabsorption in the renal tubules, nephrogenic DI results. This can occur due to genetic mutations in the vasopressin receptors, from kidney disease, or due to certain medications, such as lithium and tetracycline.

SIADH occurs when there is too much secretion of ADH despite normal or low plasma osmolality. This causes impaired water excretion, low sodium (dilutional hyponatremia), fluid retention, and concentrated urine with high osmolality despite low plasma osmolality. Tumors, trauma, or infections in the brain; pulmonary disorders such as pneumonia or small cell lung cancer; and certain medications including selective serotonin reuptake inhibitors can cause SIADH.Β 

Diagnosing and Managing ADH-Related Disorders

Diagnosing and managing ADH-related disorders involves several steps. See below to learn how:

Diagnostic Tests for ADH Imbalance

ADH function and related imbalances are evaluated using a combination of clinical evaluation, laboratory tests, and imaging studies.Β 

A thorough medical history and physical examination help to identify symptoms and signs that suggest imbalances in ADH. These can include increased thirst (polydipsia), increased urination (polyuria), increased nighttime urination (nocturia), dehydration, or fluid retention.

Urine and blood testing can help assess ADH levels as well as fluid and electrolyte imbalances. For example, serum osmolality measures the concentration of solutes in the blood. If serum osmolality is low, it can suggest SIADH, while high serum osmolality may indicate dehydration or diabetes insipidus.

Urinary osmolality is valuable for assessing the kidney's ability to concentrate or dilute urine.

Urinary osmolality is typically low in DI despite high serum osmolality, indicating that the kidneys are not properly concentrating urine. On the other hand, with SIADH, urinary osmolality is typically elevated despite low serum osmolality since the kidneys are retaining excess water.

Measuring sodium levels in the blood can also help assess ADH function. If levels of sodium are low in the blood (hyponatremia) it can suggest SIADH due to dilutional effects from water retention. If excess water is being lost in DI, sodium levels in the blood can be elevated.Β 

ADH or copeptin can also be measured in plasma or serum to directly evaluate ADH secretion. Low levels of ADH suggest central DI, while high or inappropriately normal ADH levels suggest SIADH. ADH levels can also be measured after giving a bolus of hypertonic saline or after restricting water intake to assess ADH secretion under different conditions. During a fluid deprivation test, urine osmolality and serum sodium are repeatedly measured to monitor changes in hydration status and resulting ADH release. If the urine fails to concentrate despite dehydration, this suggests impaired ADH secretion such as occurs with central DI. If the urine concentration increases significantly, this indicates that ADH secretion is intact and the issue is likely to be nephrogenic DI or SIADH.

In some cases, neuroimaging studies, such as magnetic resonance imaging (MRI) or computed tomography (CT) scans, may be needed to evaluate the hypothalamus, pituitary gland, and/or surrounding structures for abnormalities, tumors, or lesions that may be causing or contributing to ADH-related disorders.

Evaluate for potential underlying causes, including head trauma, brain tumors, infections, medications, or other medical conditions that may affect ADH secretion or responsiveness.

Management Options

The management of ADH-related disorders depends on the specific cause and resulting symptoms. Diabetes insipidus is typically managed by replacing ADH using synthetic analogs (desmopressin). This helps to correct the fluid and electrolyte imbalances. In addition, any identified underlying causes should be addressed when possible.Β 

SIADH is managed by identifying and addressing the underlying cause. Fluid intake is restricted to prevent further fluid overload. In some cases, hypertonic saline or demeclocycline may be given to increase free water excretion.

Lifestyle and ADH Regulation

Incorporating specific lifestyle considerations can also be helpful.

Hydration and ADH

Maintaining proper hydration is important for balanced ADH levels and overall health. Your individual hydration needs may vary based on many factors, such as climate, activity levels, and medical conditions, so consider working with a nutritionist or health professional to determine your individual needs.

  • Overall, to maintain adequate hydration it is important to listen to your body. Pay attention to signs of dehydration like thirst, dry mouth, fatigue, dizziness, dark-colored urine, or reduced urine output.Β 
  • Drink water with electrolytes like sea salt or coconut water when you are thirsty and aim for a pale yellow urine color.Β 
  • In general, around 3.7 liters (125 ounces) per day for men and 2.7 liters (91 ounces) for women provide adequate hydration. This can come from beverages and water-rich foods like fruits (e.g., watermelon, oranges, strawberries), vegetables (e.g., cucumber, lettuce, celery), and soups.Β 
  • When you are physically active or the weather is hotter, you may need to drink more water and be sure to balance electrolytes that are lost through sweating.Β 

Impact of Alcohol and Caffeine

Caffeinated beverages and alcohol can increase urine output, so they should be limited and always balanced with water intake.Β 

Caffeine, in coffee, tea, soda, and energy drinks, increases urine production and inhibits the action of ADH, making it less effective at promoting water reabsorption in the kidneys.Β 

Alcohol can also contribute to dehydration by impacting ADH. Alcohol inhibits ADH secretion from the pituitary gland, resulting in increased urine production and dehydration. In addition, alcohol can contribute to dehydration and electrolyte imbalances by inhibiting the reabsorption of water and electrolytes in the kidneys, exacerbating fluid loss.

[signup]

Key Takeaways

ADH serves as a pivotal regulator of water balance and plays a crucial role in maintaining homeostasis within the body. This hormone is produced in the hypothalamus and released from the posterior pituitary gland into the bloodstream in response to low blood volume or increased concentration of dissolved electrolytes and other osmolytes in the blood.Β 

In the kidneys, ADH increases the permeability of the renal tubules and collecting ducts to water. This causes more water to be reabsorbed to maintain water balance and overall homeostasis within the body.

The information in this article is designed for educational purposes only and is not intended to be a substitute for informed medical advice or care. This information should not be used to diagnose or treat any health problems or illnesses without consulting a doctor. Consult with a health care practitioner before relying on any information in this article or on this website.

Learn more

No items found.

Lab Tests in This Article

Achuff, J. (2024, February 12). The Impact of Midlife Dietary Protein Intake on Healthy Aging: Insights from the Nurses’ Health Study. Rupa Health. https://www.rupahealth.com/post/the-impact-of-midlife-dietary-protein-intake-on-healthy-aging-insights-from-the-nurses-health-study

Armstrong, M., Moore, R. A., & Kerndt, C. C. (2019). Physiology, Baroreceptors. National LIbrary of Medicine; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK538172/

Better Health Channel. (2012). Exercise - the low-down on hydration. Vic.gov.au. https://www.betterhealth.vic.gov.au/health/healthyliving/Exercise-the-low-down-on-water-and-drinks

Boone, M., & Deen, P. M. T. (2008). Physiology and pathophysiology of the vasopressin-regulated renal water reabsorption. Pflugers Archiv : European Journal of Physiology, 456(6), 1005–1024. https://doi.org/10.1007/s00424-008-0498-1

Bryant, A. (2024, March 13). Rupa Health. https://www.rupahealth.com/post/pituitary-adenomas-advances-in-diagnosis-and-management

Cleveland Clinic. (n.d.). Central Diabetes Insipidus (CDI): Symptoms, Diagnosis & Treatment. Cleveland Clinic. https://my.clevelandclinic.org/health/diseases/23515-central-diabetes-insipidus-cdi

Cleveland Clinic. (2017). Diabetes, Insipidus | Cleveland Clinic. Cleveland Clinic. https://my.clevelandclinic.org/health/diseases/16618-diabetes-insipidus

Cleveland Clinic. (2020, January 6). Nocturia. Cleveland Clinic. https://my.clevelandclinic.org/health/diseases/14510-nocturia

Cleveland Clinic. (2022a, August 3). SIADH (Syndrome of Inappropriate Antidiuretic Hormone Secretion). Cleveland Clinic. https://my.clevelandclinic.org/health/diseases/23976-siadh-syndrome-of-inappropriate-antidiuretic-hormone-secretion

Cleveland Clinic. (2022b, August 24). Polydipsia: Causes & Treatment. Cleveland Clinic. https://my.clevelandclinic.org/health/symptoms/24050-polydipsia

Cleveland Clinic. (2022c, September 13). Renin-Angiotensin-Aldosterone System (RAAS): What It Is. Cleveland Clinic. https://my.clevelandclinic.org/health/articles/24175-renin-angiotensin-aldosterone-system-raas

Cleveland Clinic. (2023, June 5). Dehydration. Cleveland Clinic. https://my.clevelandclinic.org/health/diseases/9013-dehydration

Cloyd, J. (2023a, April 10). A Functional Medicine Hypertension Protocol. Rupa Health. https://www.rupahealth.com/post/functional-medicine-hypertension-protocol

Cloyd, J. (2023b, April 14). How to Alleviate Gastrointestinal (GI) Symptoms Naturally Without Medication. Rupa Health. https://www.rupahealth.com/post/how-to-alleviate-gastrointestinal-gi-symptoms-naturally-without-medication

Cloyd, J. (2023c, July 19). A Functional Medicine Menorrhagia Protocol: Comprehensive Testing, Therapeutic Diet, and Supplements. Rupa Health. https://www.rupahealth.com/post/menorrhagia-protocol

Cloyd, J. (2023d, September 28). Integrative Medicine Approach to Treating Hypotension. Rupa Health. https://www.rupahealth.com/post/integrative-medicine-approach-to-treating-hypotension

Cloyd, J. (2023e, December 1). A Functional Medicine Protocol For Balancing Blood Sugar. Rupa Health. https://www.rupahealth.com/post/a-functional-medicine-protocol-for-balancing-blood-sugar

Cloyd, J. (2024a, January 8). The Science of Hydration: How Water Intake Affects Overall Health. Rupa Health. https://www.rupahealth.com/post/the-science-of-hydration-how-water-intake-affects-overall-health

Cloyd, J. (2024b, January 19). Understanding the Role of Kidney Function Tests in Comprehensive Health Assessments. Rupa Health. https://www.rupahealth.com/post/understanding-the-role-of-kidney-function-tests-in-comprehensive-health-assessments

Cloyd, J. (2024c, March 7). What is Hyponatremia, and How Can You Test For It? Rupa Health. https://www.rupahealth.com/post/what-is-hyponatremia-and-how-can-you-test-for-it

Cloyd, J. (2024d, March 18). Kidney Function and the Basic Metabolic Panel: What You Need to Know. Rupa Health. https://www.rupahealth.com/post/kidney-function-and-the-basic-metabolic-panel-what-you-need-to-know

Cuzzo, B., & Lappin, S. L. (2019). Vasopressin (Antidiuretic Hormone, ADH). National Library of Medicine; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK526069/

DePorto, T. (2023a, January 5). Signs you have an electrolyte imbalance & how to fix it. Rupa Health. https://www.rupahealth.com/post/electrolytes

DePorto, T. (2023b, January 10). Timeline: What Happens Inside Your Body When You Quit Smoking? Rupa Health. https://www.rupahealth.com/post/what-happens-to-our-bodies-when-we-quit-smoking-a-timeline

Devuyst, O. (2013). Vasopressin and Osmoregulation: Older Than You Thought. Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis, 33(5), 472. https://doi.org/10.3747/pdi.2013.00169

Diorio, B. (2023a, January 17). Why Most Functional Medicine Practitioners Say No To Alcohol. Rupa Health. https://www.rupahealth.com/post/why-most-functional-medicine-practitioners-say-no-to-alcohol

Diorio, B. (2023b, March 17). How to test for hypothalamic-pituitary-adrenal (HPA) axis dysfunction. Rupa Health. https://www.rupahealth.com/post/what-is-the-hypothalamic-pituitary-adrenal-hpa-axis

Henderson, K. K., & Byron, K. L. (2007). Vasopressin-induced vasoconstriction: two concentration-dependent signaling pathways. Journal of Applied Physiology (Bethesda, Md. : 1985), 102(4), 1402–1409. https://doi.org/10.1152/japplphysiol.00825.2006

Kamel, K. S., Ethier, J. H., Richardson, R. M. A., Bear, R. A., & Halperin, M. L. (1990). Urine Electrolytes and Osmolality: When and How to Use Them. American Journal of Nephrology, 10(2), 89–102. https://doi.org/10.1159/000168062

Khakham, C. (2023, March 28). An integrative medicine approach to kidney disease. Rupa Health. https://www.rupahealth.com/post/an-integrative-medicine-approach-to-kidney-disease

Marx, B., ScuvΓ©e, Γ‰., ScuvΓ©e-Moreau, J., Seutin, V., & Jouret, F. (2016). Mechanisms of caffeine-induced diuresis. MΓ©decine/Sciences, 32(5), 485–490. https://doi.org/10.1051/medsci/20163205015

McCarty, T. S., & Shah, A. D. (2023). Desmopressin. PubMed; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK554582/

Mount Sinai. (n.d.). Antidiuretic hormone blood test Information | Mount Sinai - New York. Mount Sinai Health System. https://www.mountsinai.org/health-library/tests/antidiuretic-hormone-blood-test

Mutter, C. M., Smith, T., Menze, O., Zakharia, M., & Nguyen, H. (2021). Diabetes Insipidus: Pathogenesis, Diagnosis, and Clinical Management. Cureus, 13(2). https://doi.org/10.7759/cureus.13523

Najem, O., Shah, M. M., & De Jesus, O. (2021). Serum Osmolality. PubMed; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK567764/

National Library of Medicine. (n.d.-a). Demeclocycline: MedlinePlus Drug Information. Medlineplus.gov. https://medlineplus.gov/druginfo/meds/a682103.html

National Library of Medicine. (n.d.-b). Nephrogenic diabetes insipidus: MedlinePlus Genetics. Medlineplus.gov. https://medlineplus.gov/genetics/condition/nephrogenic-diabetes-insipidus/

National Library of Medicine. (n.d.-c). Osmolality Tests: MedlinePlus Medical Test. Medlineplus.gov. https://medlineplus.gov/lab-tests/osmolality-tests/

NHS. (2021, February 15). Overview - SSRI antidepressants. Nhs.uk. https://www.nhs.uk/mental-health/talking-therapies-medicine-treatments/medicines-and-psychiatry/ssri-antidepressants/overview/

NSW Health. (2017). Urine colour chart - Beat the heat. Nsw.gov.au. https://www.health.nsw.gov.au/environment/beattheheat/Pages/urine-colour-chart.aspx

Pliquett, R. U., & Obermuller, N. (2017, April 16). Endocrine testing for the Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH). Nih.gov; MDText.com, Inc. https://www.ncbi.nlm.nih.gov/books/NBK279055/

Polhuis, K., Wijnen, A., Sierksma, A., Calame, W., & Tieland, M. (2017). The Diuretic Action of Weak and Strong Alcoholic Beverages in Elderly Men: A Randomized Diet-Controlled Crossover Trial. Nutrients, 9(7), 660. https://doi.org/10.3390/nu9070660

Preston, J. (2023, March 10). How to Improve Women’s Reproductive Health With Lab Testing. Rupa Health. https://www.rupahealth.com/post/how-to-improve-womens-reproductive-health-with-lab-testing

Preston, J. (2024, February 20). How to Differentiate Common Pituitary Gland Disorders Using Lab Testing, Imaging, and Other Evaluations. Rupa Health. https://www.rupahealth.com/post/how-to-differentiate-common-pituitary-gland-disorders-using-lab-testing-imaging-and-other-evaluations

Robertson, G. L. (2001). ANTIDIURETIC HORMONE. Endocrinology and Metabolism Clinics of North America, 30(3), 671–694. https://doi.org/10.1016/s0889-8529(05)70207-3

Shahid, Z., & Singh, G. (2018, December 9). Physiology, Hypothalamus. Nih.gov; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK535380/

Sharma, R., & Sharma, S. (2018, October 27). Physiology, Blood Volume. Nih.gov; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK526077/

Shin, J. H., Lee, H. K., Choi, C. G., Suh, D. C., Kim, C. J., Hong, S. K., & Na, D. G. (2001). MR Imaging of Central Diabetes Insipidus: A Pictorial Essay. Korean Journal of Radiology, 2(4), 222. https://doi.org/10.3348/kjr.2001.2.4.222

Sparapani, S., Millet-Boureima, C., Oliver, J., Mu, K., Hadavi, P., Kalostian, T., Ali, N., Avelar, C. M., Bardies, M., Barrow, B., Benedikt, M., Biancardi, G., Bindra, R., Bui, L., Chihab, Z., Cossitt, A., Costa, J., Daigneault, T., Dault, J., & Davidson, I. (2021). The Biology of Vasopressin. Biomedicines, 9(1), 89. https://doi.org/10.3390/biomedicines9010089

University of Rochester Medical Center. (n.d.). Osmolality (Blood) - Health Encyclopedia - University of Rochester Medical Center. Www.urmc.rochester.edu. https://www.urmc.rochester.edu/encyclopedia/content.aspx?contenttypeid=167&contentid=osmolality_blood

UT South Western Medical Center. (n.d.). 25 water-rich foods to help you stay hydrated this summer | Prevention | UT Southwestern Medical Center. Utswmed.org. https://utswmed.org/medblog/hydrating-healthy-foods/

Van Vugt, D. A., & Meites, J. (1980). Influence of endogenous opiates on anterior pituitary function. Federation Proceedings, 39(8), 2533–2538. https://pubmed.ncbi.nlm.nih.gov/6247213/

Verkman, A. S. (2012). Aquaporins in Clinical Medicine. Annual Review of Medicine, 63(1), 303–316. https://doi.org/10.1146/annurev-med-043010-193843

Weinberg, J. L. (2024a, February 29). The Neurobiology of Stress: Cortisol and Beyond. Rupa Health. https://www.rupahealth.com/post/the-neurobiology-of-stress-cortisol-and-beyond

Weinberg, J. L. (2024b, March 11). Chloride Levels: What High Results Mean. Rupa Health. https://www.rupahealth.com/post/chloride-levels-what-high-results-mean

Yasir, M., & Mechanic, O. J. (2023, March 6). Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH). Nih.gov; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK507777/

Yoshimura, H. (2023a, April 25). Integrative Approach to Treating Lung Diseases in the Geriatric Population. Rupa Health. https://www.rupahealth.com/post/integrative-approach-to-treating-lung-diseases-in-the-geriatric-population

Yoshimura, H. (2023b, November 7). The remarkable power of exercise on our health: A comprehensive overview. Rupa Health. https://www.rupahealth.com/post/the-remarkable-power-of-exercise-on-our-health-a-comprehensive-overview

Yoshimura, H. (2023c, December 18). Exploring the Connection Between Chronic Pain and Emotional Wellbeing in Functional Medicine. Rupa Health. https://www.rupahealth.com/post/exploring-the-connection-between-chronic-pain-and-emotional-wellbeing-in-functional-medicine

Yoshimura, H. (2023d, December 20). Functional Medicine for Mental Clarity: Combating Brain Fog Naturally. Rupa Health. https://www.rupahealth.com/post/functional-medicine-for-mental-clarity-combating-brain-fog-naturally

Order from 30+ labs in 20 seconds (DUTCH, Mosaic, Genova & More!)
We make ordering quick and painless β€” and best of all, it's free for practitioners.

Latest Articles

View more on Endocrinology
Subscribe to the Magazine for free
Subscribe for free to keep reading! If you are already subscribed, enter your email address to log back in.
Thanks for subscribing!
Oops! Something went wrong while submitting the form.
Are you a healthcare practitioner?
Thanks for subscribing!
Oops! Something went wrong while submitting the form.
Subscribe to the Magazine for free to keep reading!
Subscribe for free to keep reading, If you are already subscribed, enter your email address to log back in.
Thanks for subscribing!
Oops! Something went wrong while submitting the form.
Are you a healthcare practitioner?
Thanks for subscribing!
Oops! Something went wrong while submitting the form.
Trusted Source
Rupa Health
Medical Education Platform
Visit Source
Visit Source
American Cancer Society
Foundation for Cancer Research
Visit Source
Visit Source
National Library of Medicine
Government Authority
Visit Source
Visit Source
Journal of The American College of Radiology
Peer Reviewed Journal
Visit Source
Visit Source
National Cancer Institute
Government Authority
Visit Source
Visit Source
World Health Organization (WHO)
Government Authority
Visit Source
Visit Source
The Journal of Pediatrics
Peer Reviewed Journal
Visit Source
Visit Source
CDC
Government Authority
Visit Source
Visit Source
Office of Dietary Supplements
Government Authority
Visit Source
Visit Source
National Heart Lung and Blood Institute
Government Authority
Visit Source
Visit Source
National Institutes of Health
Government Authority
Visit Source
Visit Source
Clinical Infectious Diseases
Peer Reviewed Journal
Visit Source
Visit Source
Brain
Peer Reviewed Journal
Visit Source
Visit Source
The Journal of Rheumatology
Peer Reviewed Journal
Visit Source
Visit Source
Journal of the National Cancer Institute (JNCI)
Peer Reviewed Journal
Visit Source
Visit Source
Journal of Cardiovascular Magnetic Resonance
Peer Reviewed Journal
Visit Source
Visit Source
Hepatology
Peer Reviewed Journal
Visit Source
Visit Source
The American Journal of Clinical Nutrition
Peer Reviewed Journal
Visit Source
Visit Source
The Journal of Bone and Joint Surgery
Peer Reviewed Journal
Visit Source
Visit Source
Kidney International
Peer Reviewed Journal
Visit Source
Visit Source
The Journal of Allergy and Clinical Immunology
Peer Reviewed Journal
Visit Source
Visit Source
Annals of Surgery
Peer Reviewed Journal
Visit Source
Visit Source
Chest
Peer Reviewed Journal
Visit Source
Visit Source
The Journal of Neurology, Neurosurgery & Psychiatry
Peer Reviewed Journal
Visit Source
Visit Source
Blood
Peer Reviewed Journal
Visit Source
Visit Source
Gastroenterology
Peer Reviewed Journal
Visit Source
Visit Source
The American Journal of Respiratory and Critical Care Medicine
Peer Reviewed Journal
Visit Source
Visit Source
The American Journal of Psychiatry
Peer Reviewed Journal
Visit Source
Visit Source
Diabetes Care
Peer Reviewed Journal
Visit Source
Visit Source
The Journal of the American College of Cardiology (JACC)
Peer Reviewed Journal
Visit Source
Visit Source
The Journal of Clinical Oncology (JCO)
Peer Reviewed Journal
Visit Source
Visit Source
Journal of Clinical Investigation (JCI)
Peer Reviewed Journal
Visit Source
Visit Source
Circulation
Peer Reviewed Journal
Visit Source
Visit Source
JAMA Internal Medicine
Peer Reviewed Journal
Visit Source
Visit Source
PLOS Medicine
Peer Reviewed Journal
Visit Source
Visit Source
Annals of Internal Medicine
Peer Reviewed Journal
Visit Source
Visit Source
Nature Medicine
Peer Reviewed Journal
Visit Source
Visit Source
The BMJ (British Medical Journal)
Peer Reviewed Journal
Visit Source
Visit Source
The Lancet
Peer Reviewed Journal
Visit Source
Visit Source
Journal of the American Medical Association (JAMA)
Peer Reviewed Journal
Visit Source
Visit Source
Pubmed
Comprehensive biomedical database
Visit Source
Visit Source
Harvard
Educational/Medical Institution
Visit Source
Visit Source
Cleveland Clinic
Educational/Medical Institution
Visit Source
Visit Source
Mayo Clinic
Educational/Medical Institution
Visit Source
Visit Source
The New England Journal of Medicine (NEJM)
Peer Reviewed Journal
Visit Source
Visit Source
Johns Hopkins
Educational/Medical Institution
Visit Source
Visit Source

Hey Practitioners! On December 11th, join Dr. Terry Wahls in a free live class where she'll share her groundbreaking methods for managing MS and autoimmune patients. This live session will address your most pressing questions and will take a closer look at treatment options beyond the conventional standards of care. Register here.

Register Here