chapter 2 fever 1.introduction 2.causes and mechanisms of fever 3.febrile phases and the...
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Chapter 2 Fever
1.Introduction2.Causes and mechanisms of fever3.Febrile phases and the characteristics of
thermo-metabolism4.Functional and metabolic changes induced by
febrile response5.Pathophysiological basis of prevention and
treatment for fever
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1.Introduction
(1)Normal body temperature ~37℃ ( ~98.6 。 F )• Axillary 36~37 .4 C• Oral 36.7~37.7 C• Rectal 36.9~37.9 C
Normal body temperature homeostasis
(2) Elevation of body temperature An elevation of body temperature above
the normal amplitude of daily variation(>0.5℃)
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Types of the elevation of body temperaturePhysiological elevationthe setpoint of hypothalamic thermostat before menstruationsevere exercise stress
Pathological elevation •Fever
•Hyperthermia
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Fever
Fever is a complicated pathological process characterized by a regulated elevation of core body temperature that exceeds the normal daily variation (>0.5℃), in which pyrogens cause a temporary upward resetting of the hypothalamic thermostatic setpoint.
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Hyperthermia ( 过热 )
An unregulated rise in body temperature beyond the unchanged hypothalamic thermostatic setpoint resulting from the dysfunction of body temperature center or impairment of thermogenesis and heat loss mechanisms. 体温调节机制失调或调节障碍,使得机体不能将体温控制在与调定点相适应的水平而引起的非调节性的体温升高。 Causes: •overproduction of heat ( 过度产热 )•impediment in heat loss ( 散热障碍 )•dysfunction of body temperature center ( 体温调节中枢功能障碍 )
Passive increase of body temperature >0.5 C ( 被动性体温升高 )
Body temperature beyond the setpoint ( 体温 > 调定点水平 )
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Hyperthermia Fever
Arising from changes within the body or by changes in environment
Resulting from pyrogen
Set-point remains unchanged or damaged, or effector organs fails
Ability to regulate set-point remains intact, but is turned up at a high level functionally
Body temperature may rise to a very high level
Rise of body temperature has an upper limit
Treatment with water-alcohol bathing
Treatment with antipyretics and measures and drugs to eliminate the causes
Comparison between hyperthermia and fever
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2. Causes and mechanisms of fever ( 发热的原因和机制 )
(1)Pyrogenic activator ( 发热激活物 ) (2)Endogenous pyrogen ( 内生致热原 )(3)Mechanisms of set point elevation
caused by EP (EP 升高体温中枢“调定点”的机制 )(4)Pathogenesis of fever ( 发热时体温上升的基本环节和机制 )
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(1) Pyrogenic activator
Pyrogenic activator A fever-inducing substances that can activate endogenous pyrogen-generating cells to generate and release endogenous pyrogens.
Category of pyrogenic activator •Infectious factors: microbes and microbial products•Non-infectious factors: non-microbe pyrogenic activators
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•Infectious factors: microbes and microbial products
G- bacteria, Lipopolysaccharide (LPS)/endotoxinG+bacteria, Exotoxins, Cell wall peptidoglycans Viruses Other microorganisms
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•Non-infectious factors: non-microbe pyrogenic activators
Ag-Ab complexesNon-infectious inflammation-genesis irritants Steroids: etiocholanolone
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Concept of endogenous pyrogen (EP)
EPs are fever-inducing cytokines via elevating the hypothalamic thermostatic setpoint, and derived from mononuclear cells, macrophages, Kupffer cell, endothelia cells and etc under the action of pyrogenic activators.
(2)Endogenous pyrogen
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EP generating cells
Monocyte Macrophage T lymphocyte Kupffer cells endothelia cells Some tumor cells
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Category of endogenous pyrogen
Interleukin-1 (IL-1) Tumor necrosis factor (TNF) Interferon (IFN) Macrophage inflammatory protein-1 (MIP-1) Interleukin-6 (IL-6) Others
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Endogenous pyrogen
Principle source Inducers
IL-1IL-1
Macrophages and other cell types
LPS,TNF, Other microbial products
TNF-TNF-
Macrophages
Lymphocytes(T&B)
LPS, Other microbial products
antigen, mitogen stmulation
IFN- IFN- IFN-
Leukocytes
Fibloblasts
T-lymphocytes
LPS, viral infection
IL-6 Many cell types LPS, TNF
MIP-1MIP-1
Macrophages LPS
IL-8 Many cell types LPS, TNF, IL-1
Endogenous Pyrogenic cytokines
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Production and release of EP
LPS + LBP --- LPS + sCD14 --- TLR (EP-producing cells)--- NF-κB---Target genes --- EP expression and release(Textbook P143:figure 9-1)
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(3)Mechanisms of setpoint elevation by EP
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Thermoregulation center
Positive regulation center Preoptic anterior hypothalamus, POAH
Cold sensitive neuron Warm sensitive neuron
Negative regulation center : Medial amygdaloid nucleus,MAN Ventral septal area,VSA
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Three pathways for EP signal transduction to the thermoregulation center
Via organum vasculosum laminae terminalis, OVLT Via stimulation of vagus nerve Direct entry through blood-brain barrier
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EP
Macrophage
OVLT neuron
POAH neuron
Supraoptic recessThird ventricle of brain
Chiasma of optic nerves
Capillary
OVLT area
Macrophage
POAH neuron
PGE2PGE2
Cells of ventricle tubal membrane
The Role of OVLT in pathogenesis of fever
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Central mediators of fever
The positive regulation mediators Prostaglandins,PGE2 Corticotropin releasing hormone,CRH The ratio of central Na+/Ca2+
cAMP Nitric oxide, NO
Mechanisms of Setpoint Elevation by EP
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The negative regulation mediators
Febrile ceiling, Endogenous cryogen Arginine vasopressin, AVP α-melanocyte-stimulating hormone,α-MSH Lipocortin-1/Annexin A1
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(4) Pathogenesis of fever
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Pyrogenic activators:infection, microbial toxins, mediators of inflammation, immune reactions
Monocytes/macrophages, endothelial cells, others
Endogenous pyrogens/ Pyrogenic cytokines IL-1,6, TNF, IFN,MIP-1
Hypothalamus Central mediators of fever
Elevated thermoregulatory set point
Circulation, etc
Heat conservation, heat production
FEVER
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3. Febrile phases and the characteristics of thermo-metabolism
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典型的发热过程分为 3 个阶段
37C
42 C
体温正常 体温上升期 高热持续期 体温下降期
调定点上移
调定点恢复
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Effervescence period Heat production > heat loss
Persistent febrile period Heat equipoise at a higher level Defervescence period
Heat loss> heat production
Phases of fever
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4.Functional and metabolic changes induced by febrile response
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(1)Functional changes
•Central nervous system
•Cardiovascular system
•Respiratory system
•Digestive system •Immune system
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(2) Changes of metabolism
Sugar
Lipid
Protein
Walter, salts, vitamines
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5. Pathophysiological basis of prevention and treatment for fever Basic principles for fever treatment
Antipyretic therapy
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Case study