The
adrenal glands which are also called the suprarenal glands, are small,
triangular glands located on top of both kidneys. An adrenal gland is made
of two parts: the outer region is called the adrenal cortex and the inner
region is called the adrenal medulla. Both parts of the adrenal glands --
the adrenal cortex and the adrenal medulla -- perform very separate
functions.
The adrenal glands work interactively with the hypothalamus and pituitary
gland in the following process:
the hypothalamus produces corticotropin-releasing hormones, which
stimulate the pituitary gland.
the pituitary gland, in turn, produces corticotropin hormones, which
stimulate the adrenal glands to produce corticosteroid hormones.
The
outer covering (adrenal cortex) is derived from the fetal mesodermal ridge,
a structure that also gives rise to the kidneys so that the juxtaposition of
the two organs is not surprising. Within the adrenal cortex are three zones
known as the outer (zona glomerulosa), the middle (zona fasciculata), and
the inner (zona reticularis). Under the microscope the cells are rather
typical endocrine cells; the distinction between zones is made by differing
staining characteristics.
Adrenal Cortex Functions
The adrenal cortex, the outer portion of the adrenal
gland, secretes hormones that have an effect on the body's metabolism, on
chemicals in the blood, and on certain body characteristics. The adrenal cortex
secretes corticosteroids and other hormones directly into the bloodstream. The
hormones produced by the adrenal cortex include:
corticosteroid hormones
hydrocortisone hormone - this hormone, also known
as cortisol, controls the body's use of fats, proteins, and carbohydrates.
corticosterone - this hormone, together with
hydrocortisone hormones, suppresses inflammatory reactions in the body and also
affects the immune system.
aldosterone hormone - this hormone inhibits the
level of sodium excreted into the urine, maintaining blood volume and blood
pressure.
androgenic steroids (androgen hormones) - these
hormones have minimal effect on the development of male characteristics
Adrenocortical cells synthesize and secrete chemical
derivatives (steroids) from
cholesterol, the major animal sterol. While cholesterol can be
synthesized in many body tissues, further differentiation into
steroid hormones takes place only in the adrenal cortex and in its
embryological cousins, the ovaries and the testes.
The adrenal cortex is capable of synthesizing all of the steroid hormones
produced by the body, including the progestogens and estrogens (see
the ovary), androgens (see
the testis), mineralocorticoids (which are
secreted from the zona glomerulosa), and glucocorticoids (which are
synthesized and released from the zona fasciculata and zona reticularis of
the adrenal cortex). Although upwards of 60 steroids are manufactured in the
adrenal cortex, only a few members of these three major categories are
important in body functioning.
The biologic effect of aldosterone, the principal
mineralocorticoid, is to set in motion a
set of reactions at the cell surface of all body tissues in order to enhance
the uptake and retention of sodium in all cells and the extrusion of
potassium from them. It also has a major impact on kidney function, to retain sodium within the circulation while increasing the
excretion of potassium into the urine. At the same time, aldosterone tends to decrease the
acidity of body fluids.
Cortisol (hydrocortisone) is the major human
glucocorticoid. It exerts multiple and varied effects. It also serves as a
mineralocorticoid but is considerably less effective than aldosterone.
Cortisol plays a major role in the body's response to stress. In fasting,
for example, it sustains the blood sugar concentration by blocking the
egress of glucose into all tissues other than the critically important brain
and spinal cord, while it simultaneously increases the breakdown of protein
from muscle and other organs and hastens the conversion of newly generated
amino acids to glucose to replenish the supply constantly being consumed by
the brain.
Cortisol, along with more potent and longer-acting
synthetic derivatives like prednisone, methylprednisolone, and dexamethasone
exerts powerful anti-inflammatory effects. Physicians take advantage of
these properties in treating patients with serious inflammatory illnesses
such as rheumatoid arthritis, disseminated lupus erythematosus, and multiple
sclerosis. If, however, the inflammation has a bacterial or viral origin,
the steroids may do more harm than good because the spread of the infection
is facilitated while the signs of inflammation are masked (see
immune system). Finally,
corticosteroids in large doses impair the functioning of the immune system
so that the production of harmful antibodies, such as those produced in
allergic diseases, may be suppressed. It is important to note that these
beneficial effects are offset by serious side effects of large-dose,
long-term corticosteroid therapy, effects that closely mimic many of the
symptoms of Cushing's syndrome (see below).
Adrenal androgens are not as potent as testosterone,
the major steroid secreted by the testis, but a number of them, including androstenedione, dehydroepiandrosterone (DHEA), and its sulfate (DHEAS) may
be converted to stronger androgens such as testosterone. Although little
androgen is secreted before puberty, the output increases dramatically at
puberty so that the adrenal cortex makes a significant contribution, known
as the adrenarche, to developmental changes in both sexes.
The three classes of corticosteroids (the
mineralocorticoids, the glucocorticoids, and the adrenal androgens) are
regulated largely by separate mechanisms. Glucocorticoids are regulated by
way of the classical hypothalamic-hypophyseal feedback system. Within the
family of glucocorticoids, the cortisol level is the one most closely
guarded. Furthermore, the ongoing feedback control is modulated by
hypothalamic biorhythmic activity illustrated in the case of cortisol in the
figure to the left. When the individual is exposed to physical or emotional
stress, the self-regulating mechanism is interrupted and plasma cortisol is
increased to deal with the stress. Adrenal androgen secretion is controlled
primarily by ACTH, although there is evidence that prolactin stimulates the
secretion of adrenal androgens as well.
Aldosterone secretion is modulated directly by serum
electrolyte levels. Lowered serum sodium concentrations enhance aldosterone
secretion, but a far more potent stimulus is a high serum potassium level.
Aldosterone increases the reabsorption of sodium (and the excretion of potassium)
by the
distal tubules in the kidney. The reabsorption of sodium results in an
increased reabsorption of water which can result in hypertension. Low blood
aldosterone levels are seen in {addisons} Addison's disease and toxemia of pregnancy.
Higher levels can be seen in {cushings} Cushing's syndrome, primary hyperaldosteronism,
malignant hypertension, severe swelling in congestive heart failure, and
nephrotic syndrome.
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