Biomedical Engineering Reference
In-Depth Information
Table 8.24. Eicosanoids associated with blood circulation (taken from [ 813 ], with permission).
( Part 1 ) Prostaglandins and prostacyclins (L
: lymphocyte; TC: thrombocyte [platelet]; WBC:
white blood cell [leukocyte]; Bdk: bradykinin; His: histamine; IL: interleukin). Prostaglandin-
H2 (PGh2) is a precursor of 5 types of prostanoids using specific prostanoid synthases (PGdS,
PGeS, PGfS, and PGiS) that connect to their specific binding sites in PGh2 molecule. The
number (2) refers to the number of carbon-carbon double bonds. Synthesis of prostanoids
prostaglandins, which are mediators of inflammatory and anaphylactic reactions, thromboxanes,
which are vasoconstrictors, and prostacyclins, which operate in the resolution of inflammation,
involves a sequence of 3 stages: (1) release of arachidonic acid from phospholipids by secretory
and/or cytoplasmic phospholipase A2 (sPLA2 and cPLA2); (2) oxygenation of arachidonic acid
by cyclooxygenases to form PGh2; and (3) conversion of PGh2 to prostaglandin-D2 (PGd2),
prostaglandin-E2 (PGe2), prostaglandin-F2
ϕ
), prostacyclin (PGi2), and thromboxane-
A2 (TxA2) via 7 specific synthases, including thromboxane synthase (TxAS). Two PGdS
subtypes comprise hematopoietic (hPGdS) and lipocalin (lPGdS) synthases. Three isoforms of
PGE synthase (PGeS) encompass microsomal mPGeS1 and mPGeS2 and cytoplasmic cPGeS
enzymes.
α
(PGf2
α
Type
Synthesis site
Activity
PGd2
Mastocyte
Vasodilation
Inhibition of TC and WBC aggregation
Reduction in T-cell proliferation
Decrease in L
migration
Secretion of IL1a/2
ϕ
PGe2
Heart,
Vasodilation
kidney, spleen
TC aggregation
Reduction in T-cell proliferation
Decrease in L
migration
Secretion of IL1a/2
ϕ
Enhancement of Bdk and His effects
PGf2
α
Heart,
Vasoconstriction,
kidney, spleen
bronchoconstriction
PGh2
Widespread precursor
Vasoconstriction
TC aggregation
PGi2
EC
Vasodilation
Inhibition of TC and WBC aggregation
Reduction in T-cell proliferation
Decrease in L
migration
Reduced secretion of IL1a and IL2
ϕ
Reactive Oxygen Species
The pulmonary circulation is very sensitive to changes in the blood partial pres-
sure of oxygen. Pulmonary vessels contract in response to low oxygen content
in blood, whereas systemic vessels dilate [ 816 ]. Reversible vasoconstriction of
pulmonary artery smooth myocytes is a compensatory response that redirects blood
to better ventilated lung regions. Pulmonary vessel constriction also results from an
 
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