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CORTICOSTEROIDS
 INTROUDCTION
Corticosteroids (CSs) are a class of steroid hormones that are
produced and secreted by the adrenal glands in response to
pituitary adrenocroticotropic hormone, and regulated by
hypothalamic croticotropin releasing hormone.
These hormones are responsible for regulating major endocrine
system functions, including managing stress and controlling
homeostasis. The main CSs produced by the adrenal cortex are
cortisol (glucocorticoids) and aldosterone (mineralocorticoids).
Aldosterone influences sodium and water balance, while cortisol
exerts its effect by preventing the release of inflammation
mediators, high blood cortisol levels were discovered in cushingoid
patients and its anti-inflammatory effects were first demonstrated in
patients with rheumatoid arthritis. Since then, numerous
investigators have established the ability of physiologic levels of
these hormones to alter inflammation and immune functions.3-6
Currently, CSs find use in the treatment of various neurological
diseases, inflammation, pain, autoimmune disorders, and cancer.
The various chemical structural differences between natural
and synthetic steroids, discuss their pharmacokinetic and
pharmacodynamic profiles, and describe their use in neurocritical
care clinical practice.
PHARMOACKINETICS
Cortisol is present within the plasma in three different forms; free
cortisol, protein bound, and cortisol metabolite.
About 5% of circulating cortisol is unbound and, roughly, 80% of the
circulating cortisol is bound to cortisol binding globulin (CBG) or
albumin. During inflammation, the binding affinity of cortisol
declines, rendering a higher free cortisol concentration at the site of
interest to alleviate the active inflammatory process. Most synthetic
CSs are also found bound to CBG, however, these glucocorticoids
analogues bind less efficiently compared to native cortisol. Cortisol
metabolites are biologically inactive and bind weakly to circulating
plasma proteins
 chemical modifications of natural steroids revealed a number
of structural features essential for their biological activities.
Cortisol includes a cyclopentenoperhydrophenanthrene
nucleus, made up of three 6-carbon rings and a single 5-
carbon pentane ring. Cortisol has 21 carbon atoms with a 2-
carbon side chain attached to position 17 and methyl groups
at C-10 and C-13. Chemical alterations at various positions of
the steroid molecule lead to synthetic analogous of cortisol
with increased glucocorticoid and/or mineralocorticoid
activities.
For example, cortisone is derived from cortisol by
substituting the hydroxyl group at C-11 with a carbonyl group,
whereas prednisolone results from the addition of a double
bond between the C-1 and C-2 positions of cortisol;
methylation of prednisolone at C-6 produces
methylprednisolone. Glucocorticoids that are fluorinated at
the 9-alpha position include dexamethasone, fludrocortisone
and betamethasone.
Both cortisone and prednisone must be converted to the
active metabolites cortisol and prednisolone, respectively,
prior exerting their action.
A slight change in the molecular structure introduces a
variety of synthetic glucocorticoids with diverse potency, half-
lives, and mineralocorticoid activities. Some are far more
potent than cortisol, and their different pharmacodynamic
and pharmacokinetic activities gave them unique
characteristic. common orally available corticosteroids and
compares their potency and mineralocorticoids activity.
PHARMACODYNAMIC OF
CORTICOSTEROIDS
Corticosteroids exert their anti-inflammatory and
immunosuppressive effects by interrupting multiple steps in
the up- regulation of the immune system. Their suppressive
activity is predominantly restricted to cell-mediated
immunity.
It is believed that CS inhibit antigen presentation, cytokine
production and lymphocytes proliferation by binding to
glucocorticoid receptors found throughout the body. In
response to
CS administration, lymphocytopenia is induced as a result of
redistribution of circulating lymphocytes into other lymphoid
compartments.
A single dose of CS produces lymphocytopenia within 4 hours of
administration which normalizes through redistribution into the
circulation away from periphery, rather than destruction, within 24
to 48 hours. Similarly, monocytes and eosinophils, which normally
accumulate at the inflammatory site, decrease upon administration
of CSs. In contrast, CSs induce neutrophilia via the release of
neutrophils from the bone marrow into the circulation, reduction in
the migration of neutrophils out of the circulation, and
demargination of neutrophils from the vascular lining. The anti-
inflammatory process mediated by CSs is multimodal and begins
with synthesis of lipocortin-1, which then suppresses phospholipase
A2, thereby blocking eicosanoid production, and further inhibiting
various leukocyte inflammatory events. The end result of this
process is inhibition of prostaglandin synthesis and cyclooxygenase
(COX-1 and COX-2), thus potentiating the anti-inflammatory effect.
Individual steroids
Relative potencies Glucocorticoid Mineralocorticoid
Hydrocortisone 1 1
Cortisol 1.25 1
Prednisolone 4 0.8
Methylprednisolone 5 minimal
Dexamethasone 30 minimal
Fludrocortisone 15 150
 methylprednisolone used for IV pulsed therapy
 prednisolone is standard choice for anti-inflammatory
therapy. Can be given orally or IM
 dexamethasone longer acting.
 fludrocortisone used to replace aldosterone where the
adrenal cortex has been destroyed
 beclomethasone and budesonide used by inhalation for
asthma. About 90% of inhalation dose is swallowed and
inactivated by first-pass hepatic metabolism (steroids
listed above are protected from this by protein binding).
The rest, which is absorbed from the mouth and lungs
gives very low systemic plasma concentrations. Although
risk of HPA axis suppression is very low it can happen.
 Mechanism of action
 enter cells where they combine with steroid
receptors in cytoplasm
 combination enters nucleus where it controls
synthesis of protein, including enzymes that regulate vital
cell activities over a wide range of metabolic functions
including all aspects of inflammation
 formation of a protein that inhibits the enzyme
phospholipase A2 which is needed to allow the supply
of arachidonic acid. Latter is essential for the formation of
inflammatory mediators
 also act on cell membranes to alter ion permeability
 also modify the production of neurohormones
 side effects of corticosteroids
Corticosteroids have many side effects that can be mild or serious.
These side effects are more apparent when corticosteroids are
used at higher doses or for extended periods of time. This section
lists only some of these side effects of corticosteroids.
Corticosteroids can:
 cause sodium (salt) and fluid to be retained in the body and cause
weight gain or swelling of the legs (edema)
 High blood pressure
 Loss of potassium
 Headache
 Muscle weakness
 Puffiness of the face (moon face)
 Facial hair growth
 Thinning and easy bruising of the skin
 Slow wound healing
 Glaucoma
 Cataracts
 Ulcers in the stomach and duodenum
 Loss of diabetes control
 Menstrual irregularity
 "Buffalo hump," a condition described as a rounding of the upper
back
The prolonged use of corticosteroids can cause obesity, growth
retardation in children, and even lead to convulsions and
psychiatric disturbances. Reported psychiatric disturbances
include depression, euphoria, insomnia, mood swings, and
personality changes. Psychotic behaviors also have been reported.

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CORTICOSTEROIDS

  • 1. CORTICOSTEROIDS  INTROUDCTION Corticosteroids (CSs) are a class of steroid hormones that are produced and secreted by the adrenal glands in response to pituitary adrenocroticotropic hormone, and regulated by hypothalamic croticotropin releasing hormone. These hormones are responsible for regulating major endocrine system functions, including managing stress and controlling homeostasis. The main CSs produced by the adrenal cortex are cortisol (glucocorticoids) and aldosterone (mineralocorticoids). Aldosterone influences sodium and water balance, while cortisol exerts its effect by preventing the release of inflammation mediators, high blood cortisol levels were discovered in cushingoid patients and its anti-inflammatory effects were first demonstrated in patients with rheumatoid arthritis. Since then, numerous investigators have established the ability of physiologic levels of these hormones to alter inflammation and immune functions.3-6
  • 2. Currently, CSs find use in the treatment of various neurological diseases, inflammation, pain, autoimmune disorders, and cancer. The various chemical structural differences between natural and synthetic steroids, discuss their pharmacokinetic and pharmacodynamic profiles, and describe their use in neurocritical care clinical practice. PHARMOACKINETICS Cortisol is present within the plasma in three different forms; free cortisol, protein bound, and cortisol metabolite. About 5% of circulating cortisol is unbound and, roughly, 80% of the circulating cortisol is bound to cortisol binding globulin (CBG) or albumin. During inflammation, the binding affinity of cortisol declines, rendering a higher free cortisol concentration at the site of interest to alleviate the active inflammatory process. Most synthetic CSs are also found bound to CBG, however, these glucocorticoids analogues bind less efficiently compared to native cortisol. Cortisol metabolites are biologically inactive and bind weakly to circulating plasma proteins  chemical modifications of natural steroids revealed a number of structural features essential for their biological activities. Cortisol includes a cyclopentenoperhydrophenanthrene nucleus, made up of three 6-carbon rings and a single 5- carbon pentane ring. Cortisol has 21 carbon atoms with a 2- carbon side chain attached to position 17 and methyl groups at C-10 and C-13. Chemical alterations at various positions of the steroid molecule lead to synthetic analogous of cortisol
  • 3. with increased glucocorticoid and/or mineralocorticoid activities. For example, cortisone is derived from cortisol by substituting the hydroxyl group at C-11 with a carbonyl group, whereas prednisolone results from the addition of a double bond between the C-1 and C-2 positions of cortisol; methylation of prednisolone at C-6 produces methylprednisolone. Glucocorticoids that are fluorinated at the 9-alpha position include dexamethasone, fludrocortisone and betamethasone. Both cortisone and prednisone must be converted to the active metabolites cortisol and prednisolone, respectively, prior exerting their action. A slight change in the molecular structure introduces a variety of synthetic glucocorticoids with diverse potency, half- lives, and mineralocorticoid activities. Some are far more potent than cortisol, and their different pharmacodynamic and pharmacokinetic activities gave them unique characteristic. common orally available corticosteroids and compares their potency and mineralocorticoids activity. PHARMACODYNAMIC OF CORTICOSTEROIDS Corticosteroids exert their anti-inflammatory and immunosuppressive effects by interrupting multiple steps in the up- regulation of the immune system. Their suppressive activity is predominantly restricted to cell-mediated immunity. It is believed that CS inhibit antigen presentation, cytokine production and lymphocytes proliferation by binding to glucocorticoid receptors found throughout the body. In response to
  • 4. CS administration, lymphocytopenia is induced as a result of redistribution of circulating lymphocytes into other lymphoid compartments. A single dose of CS produces lymphocytopenia within 4 hours of administration which normalizes through redistribution into the circulation away from periphery, rather than destruction, within 24 to 48 hours. Similarly, monocytes and eosinophils, which normally accumulate at the inflammatory site, decrease upon administration of CSs. In contrast, CSs induce neutrophilia via the release of neutrophils from the bone marrow into the circulation, reduction in the migration of neutrophils out of the circulation, and demargination of neutrophils from the vascular lining. The anti- inflammatory process mediated by CSs is multimodal and begins with synthesis of lipocortin-1, which then suppresses phospholipase A2, thereby blocking eicosanoid production, and further inhibiting various leukocyte inflammatory events. The end result of this process is inhibition of prostaglandin synthesis and cyclooxygenase (COX-1 and COX-2), thus potentiating the anti-inflammatory effect. Individual steroids Relative potencies Glucocorticoid Mineralocorticoid Hydrocortisone 1 1 Cortisol 1.25 1 Prednisolone 4 0.8 Methylprednisolone 5 minimal Dexamethasone 30 minimal Fludrocortisone 15 150
  • 5.  methylprednisolone used for IV pulsed therapy  prednisolone is standard choice for anti-inflammatory therapy. Can be given orally or IM  dexamethasone longer acting.  fludrocortisone used to replace aldosterone where the adrenal cortex has been destroyed  beclomethasone and budesonide used by inhalation for asthma. About 90% of inhalation dose is swallowed and inactivated by first-pass hepatic metabolism (steroids listed above are protected from this by protein binding). The rest, which is absorbed from the mouth and lungs gives very low systemic plasma concentrations. Although risk of HPA axis suppression is very low it can happen.  Mechanism of action  enter cells where they combine with steroid receptors in cytoplasm  combination enters nucleus where it controls synthesis of protein, including enzymes that regulate vital cell activities over a wide range of metabolic functions including all aspects of inflammation  formation of a protein that inhibits the enzyme phospholipase A2 which is needed to allow the supply of arachidonic acid. Latter is essential for the formation of inflammatory mediators
  • 6.  also act on cell membranes to alter ion permeability  also modify the production of neurohormones  side effects of corticosteroids Corticosteroids have many side effects that can be mild or serious. These side effects are more apparent when corticosteroids are used at higher doses or for extended periods of time. This section lists only some of these side effects of corticosteroids. Corticosteroids can:  cause sodium (salt) and fluid to be retained in the body and cause weight gain or swelling of the legs (edema)
  • 7.  High blood pressure  Loss of potassium  Headache  Muscle weakness  Puffiness of the face (moon face)  Facial hair growth  Thinning and easy bruising of the skin  Slow wound healing  Glaucoma  Cataracts  Ulcers in the stomach and duodenum  Loss of diabetes control  Menstrual irregularity  "Buffalo hump," a condition described as a rounding of the upper back The prolonged use of corticosteroids can cause obesity, growth retardation in children, and even lead to convulsions and psychiatric disturbances. Reported psychiatric disturbances include depression, euphoria, insomnia, mood swings, and personality changes. Psychotic behaviors also have been reported.