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Related Concept Videos

Inflammation01:38

Inflammation

Overview
Acute Inflammation I: Inflammatory Response01:26

Acute Inflammation I: Inflammatory Response

Acute inflammation is a rapid, short-lived physiological response to tissue injury or infection, designed to eliminate harmful agents and initiate repair. This tightly regulated process typically lasts from minutes to several days and is triggered by factors such as microbial invasion, physical trauma, or chemical injury.Recognition and Mediator ReleaseThe inflammatory response begins when resident immune cells—such as mast cells, macrophages, and dendritic cells—detect damage-associated...
Inflammatory Response I: Vascular and Cellular01:30

Inflammatory Response I: Vascular and Cellular

The inflammatory response is the body's defense against infection, injury, or irritation from bacteria, trauma, toxins, or heat. Inflammation helps locate and destroy pathogens and remove damaged tissue elements to heal the body. During this initial phase, fluid, blood products, and nutrients migrate to the injured area, resulting in redness, heat, swelling, ache, and loss of function. Moreover, signs of systemic inflammation include fever, increased WBC count, malaise, anorexia, nausea,...
Acute Inflammation III: Local and Systemic Effects01:25

Acute Inflammation III: Local and Systemic Effects

Acute inflammation produces a coordinated set of local and systemic changes that limit injury, eliminate pathogens, and initiate repair. These responses arise within minutes of infection, trauma, or chemical insult and are driven by vascular alterations and leukocyte-derived mediators. When the stimulus resolves, the reaction typically abates within days.Local EffectsAt the site of injury, arteriolar vasodilation increases blood flow, resulting in redness and warmth. Simultaneously, increased...
Complement System01:27

Complement System

The complement system is a group of approximately 20 plasma proteins that strengthen the body's defenses against infections through opsonization, inflammation, and cell lysis. Opsonization involves coating pathogens with complement proteins, making them more recognizable and facilitating phagocyte engulfment. Certain complement proteins induce inflammation that attracts immune cells to the site of infection. Cell lysis involves the destruction of pathogens through the formation of a membrane...
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors01:30

Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors

Angiotensin-converting enzyme (ACE), a vital component of the renin-angiotensin-aldosterone system, is abundant in lung endothelial cells. ACE converts the inactive decapeptide, angiotensin I, into the active octapeptide, angiotensin II. This potent vasoconstrictor narrows blood vessels, increasing resistance to blood flow and elevating blood pressure. Angiotensin II also stimulates aldosterone production, encouraging kidney cells to reabsorb more sodium and water from urine, thereby increasing...

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Related Experiment Video

Updated: Jun 17, 2026

Characterizing Modulators of Protease-Activated Receptors with a Calcium Mobilization Assay Using a Plate Reader
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Characterizing Modulators of Protease-Activated Receptors with a Calcium Mobilization Assay Using a Plate Reader

Published on: May 24, 2024

Activated protein C action in inflammation.

Pranita P Sarangi1, Hyun-wook Lee, Minsoo Kim

  • 1Department of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA.

British Journal of Haematology
|December 10, 2009
PubMed
Summary
This summary is machine-generated.

Activated protein C (APC) has anti-inflammatory and anti-apoptotic effects beneficial in treating severe sepsis. These cytoprotective functions, not its anticoagulant properties, are key to APC

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Characterizing Modulators of Protease-Activated Receptors with a Calcium Mobilization Assay Using a Plate Reader
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Increased Recovery Time and Decreased LPS Administration to Study the Vagus Nerve Stimulation Mechanisms in Limited Inflammatory Responses
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Increased Recovery Time and Decreased LPS Administration to Study the Vagus Nerve Stimulation Mechanisms in Limited Inflammatory Responses

Published on: March 29, 2017

Area of Science:

  • Biochemistry
  • Critical Care Medicine
  • Pharmacology

Background:

  • Activated protein C (APC) is a natural anticoagulant regulating coagulation homeostasis.
  • APC exhibits cytoprotective effects, including anti-inflammatory and anti-apoptotic properties.
  • Recombinant human APC (rhAPC) is approved for severe sepsis treatment.

Purpose of the Study:

  • To investigate the therapeutic mechanisms of APC in severe sepsis.
  • To evaluate the role of APC's cytoprotective versus anticoagulant effects in sepsis treatment.

Main Methods:

  • Review of existing literature on APC's functions and clinical use in sepsis.
  • Analysis of clinical trial data and mechanistic studies related to APC therapy.

Main Results:

  • APC's anticoagulant effects are not solely responsible for its therapeutic benefits in sepsis.
  • APC's anti-inflammatory and anti-apoptotic actions are crucial for mitigating sepsis-induced organ damage.
  • Clinical efficacy of APC in sepsis is linked to its cytoprotective rather than anticoagulant activity.

Conclusions:

  • The cytoprotective effects of APC are the primary drivers of its therapeutic benefit in severe sepsis.
  • APC's anti-inflammatory and anti-apoptotic actions offer a novel therapeutic strategy for sepsis management.
  • Further research should focus on leveraging APC's cytoprotective properties for sepsis treatment.