Synthesis of adrenocortical hormones

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Synthesis of adrenocortical hormones

Endocrine System

Endocrine System

Pituitary gland histology
Thyroid and parathyroid gland histology
Pancreas histology
Adrenal gland histology
Synthesis of adrenocortical hormones
Adrenocorticotropic hormone
Growth hormone and somatostatin
Hunger and satiety
Antidiuretic hormone
Thyroid hormones
Insulin
Insulins
Glucagon
Somatostatin
Cortisol
Testosterone
Estrogen and progesterone
Oxytocin and prolactin
Parathyroid hormone
Calcitonin
Vitamin D
Phosphate, calcium and magnesium homeostasis
Congenital adrenal hyperplasia
Adrenal insufficiency: Pathology review
Primary adrenal insufficiency
Waterhouse-Friderichsen syndrome
Hyperaldosteronism
Cushing syndrome and Cushing disease: Pathology review
Cushing syndrome
Conn syndrome
Pheochromocytoma
Adrenal masses: Pathology review
Adrenal masses and tumors: Clinical
Adrenal cortical carcinoma
Thyroglossal duct cyst
Hyperthyroidism
Hyperthyroidism: Pathology review
Graves disease
Thyroid eye disease (NORD)
Toxic multinodular goiter
Euthyroid sick syndrome
Hypothyroidism
Hypothyroidism: Pathology review
Hashimoto thyroiditis
Hypothyroidism and thyroiditis: Clinical
Subacute granulomatous thyroiditis
Riedel thyroiditis
Thyroid storm
Thyroid nodules and thyroid cancer: Pathology review
Thyroid cancer
Thyroid nodules and thyroid cancer: Clinical
Parathyroid disorders and calcium imbalance: Pathology review
Parathyroid conditions and calcium imbalance: Clinical
Hyperparathyroidism
Hypoparathyroidism
Hypercalcemia
Hypocalcemia
Diabetes mellitus
Diabetes mellitus: Pathology review
Diabetes mellitus: Clinical
Diabetic nephropathy
Diabetic retinopathy
Pancreatic neuroendocrine neoplasms
Gigantism
Acromegaly
Hyperprolactinemia
Diabetes insipidus and SIADH: Pathology review
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Pituitary adenoma
Hypopituitarism: Pathology review
Hypopituitarism
Hyperpituitarism
Pituitary tumors: Pathology review
Pituitary apoplexy
Sheehan syndrome
Prolactinoma
Hypoprolactinemia
Constitutional growth delay
Puberty and Tanner staging
Precocious puberty
Delayed puberty
Kallmann syndrome
Disorders of sex chromosomes: Pathology review
5-alpha-reductase deficiency
Menstrual cycle
Polycystic ovary syndrome
Premature ovarian failure
Menopause
Androgen insensitivity syndrome
Autoimmune polyglandular syndrome type 1 (NORD)
Multiple endocrine neoplasia: Pathology review
Multiple endocrine neoplasia
Carcinoid syndrome
Neuroblastoma
Opsoclonus myoclonus syndrome (NORD)
Hyperthyroidism medications
Hypothyroidism medications
Hypoglycemics: Insulin secretagogues
Miscellaneous hypoglycemics
Mineralocorticoids and mineralocorticoid antagonists
Adrenal hormone synthesis inhibitors

Transcript

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The adrenal glands are two glands that sit like a hat, one on top of each kidney. Each one has an inner layer called the medulla and an outer layer called the cortex.

The adrenal cortex is subdivided into three more layers, the zona glomerulosa, zona fasciculata, and the zona reticularis, which secrete steroid hormones under the control of adrenocorticotropic hormone, or ACTH.

Adrenocorticotropic hormone is released by the anterior pituitary gland and binds to receptors on adrenal cortex cells in all three layers, and makes them take up cholesterol from the blood.

ACTH also stimulates an enzyme called cholesterol desmolase inside these cells, which converts cholesterol to pregnenolone, which is the precursor to all of the adrenal cortex hormones.

The outermost layer is the zona glomerulosa, and it’s full of cells that make the hormone aldosterone.

The first step in aldosterone production is when an enzyme called 3 beta- hydroxysteroid dehydrogenase, (or 3 beta- HSD) turns pregnenolone into progesterone.

Next, progesterone is turned into 11 deoxycorticosterone (or 11- DOC) by the enzyme 21 hydroxylase. 11 deoxycorticosterone then gets turned into corticosterone by the enzyme 11 beta-hydroxylase.

And finally, corticosterone is turned into aldosterone by the enzyme aldosterone synthase. Whew! That’s like going through the washing machine twice.

Aldosterone synthase is stimulated by the hormone angiotensin II, which is produced in the lungs in response to decreased blood volume and blood pressure.

So the final result is aldosterone which belongs to a group of hormones called mineralocorticoids, which help regulate the body’s sodium concentration.

Aldosterone binds to receptors on the cells that line the distal tubules and collecting ducts in the kidney, and increases the expression of sodium/potassium ion pumps, which are on the basolateral surface of the cells - the side facing the blood.

These ion pumps drive potassium from the blood into the cells and from there it flows down its concentration gradient into the tubule to be excreted as urine.

At the same time, the pumps drive sodium in the opposite direction from the cell into the blood, which allows more sodium to flow from the tubule into the cell down its concentration gradient.

When Na+ is reabsorbed back into the blood, water also moves into the blood, and that increases blood volume and blood pressure.

Moving on from the zona glomerulosa, the middle layer of the adrenal cortex is the zona fasciculata, and the cells there make the hormone cortisol. This process starts when pregnenolone and progesterone move into the zona fasciculata.

The enzyme 17 alpha-hydroxylase turns pregnenolone into 17 alpha- hydroxypregnenolone and turns progesterone into 17 alpha hydroxyprogesterone.

17 alpha hydroxypregnenolone is then turned into 17 alpha hydroxyprogesterone by the enzyme 3 beta- hydroxysteroid dehydrogenase.

Then, all of the 17 alpha hydroxyprogesterone is turned into 11 deoxycortisol by the enzyme 21 hydroxylase.

11 deoxycortisol is finally turned into cortisol by the enzyme 11 beta-hydroxylase.

Key Takeaways

Adrenocortical hormones are synthesized in the adrenal cortex, part of the adrenal glands located above the kidneys. The hormones are synthesized from cholesterol by a series of biochemical reactions catalyzed by enzymes. The first step is the conversion of cholesterol to pregnenolone, then pregnenolone is converted to progesterone, androgens, and glucocorticoids. Further modifications of these molecules give rise to the different adrenocortical hormones, including aldosterone, cortisol, and androstenedione.

Sources

  1. "Medical Physiology" Elsevier (2016)
  2. "Physiology" Elsevier (2017)
  3. "Human Anatomy & Physiology" Pearson (2018)
  4. "Principles of Anatomy and Physiology" Wiley (2014)
  5. "ACTH protects against glucocorticoid-induced osteonecrosis of bone" Proceedings of the National Academy of Sciences (2010)
  6. "Emerging Roles of the Mineralocorticoid Receptor in Pathology: Toward New Paradigms in Clinical Pharmacology" Pharmacological Reviews (2015)
  7. "Extra-adrenal glucocorticoids and mineralocorticoids: evidence for local synthesis, regulation, and function" American Journal of Physiology-Endocrinology and Metabolism (2011)
  8. "G Protein-Coupled Receptors: Extranuclear Mediators for the Non-Genomic Actions of Steroids" International Journal of Molecular Sciences (2014)