Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Mechanistic Models: Overview of Compartment Models01:21

Mechanistic Models: Overview of Compartment Models

68
Mechanistic models, a category encompassing both physiological and compartmental modeling, differ from empirical models' approaches to incorporating known factors about the systems being modeled. Empirical models describe data with minimal assumptions, while mechanistic models aim to provide a robust description of available data by specifying assumptions and integrating known factors about the system. Compartmental analysis is a key example of a mechanistic model in pharmacokinetics and...
68
Multicompartment Models: Overview01:14

Multicompartment Models: Overview

102
Multicompartment models are mathematical constructs that depict how drugs are distributed and eliminated within the body. They segment the body into several compartments, symbolizing various physiological or anatomical areas connected through drug transfer processes such as absorption, metabolism, distribution, and elimination.
These models offer a more comprehensive representation of drug behavior in the body than one-compartment models. They accommodate the complexity of drug distribution,...
102
Two-Compartment Open Model: Overview01:05

Two-Compartment Open Model: Overview

98
Multicompartmental models are crucial tools in pharmacokinetics, providing a framework to understand how drugs move within the body. The two-compartment model is a crucial subtype, segmenting the body into central and peripheral compartments. The central compartment represents areas with high blood flow, such as plasma and highly perfused organs like the kidneys and liver, while the peripheral compartment signifies tissues with lower blood flow, like adipose tissue and muscle tissue.
The...
98
Three-Compartment Open Model01:06

Three-Compartment Open Model

152
The three-compartment open model is a pharmacokinetic model used to describe the distribution and elimination of drugs following extravascular administration. It comprises a central compartment representing the plasma and two peripheral compartments. The highly perfused peripheral compartment represents organs and tissues with a rich blood supply, such as the liver, kidneys, and lungs. The scarcely perfused peripheral compartment represents tissues with lower blood supply, such as adipose...
152
Model Approaches for Pharmacokinetic Data: Compartment Models01:14

Model Approaches for Pharmacokinetic Data: Compartment Models

79
Compartmental analysis is a widely adopted approach to characterizing drug pharmacokinetics. It uses compartment models that conceptualize the body as a collection of reversibly communicating compartments, each representing a group of tissues exhibiting similar drug distribution characteristics. The movement rate of the drug between these compartments is typically described by first-order kinetics.
Two primary types of compartment models are recognized: mammillary and catenary. The more...
79
Compartment Models: Single-Compartment Model01:14

Compartment Models: Single-Compartment Model

2.2K
The single-compartment model serves as a simplified representation of the human body. This model assumes that the body functions as a single, well-mixed open compartment. When a drug is administered intravenously, it enters the body and quickly distributes uniformly. The drug then undergoes biotransformation and elimination, ultimately leaving the body. The volume of this compartment is referred to as the apparent volume of distribution into which the drug can uniformly distribute. In this...
2.2K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

[Analysis and prospects of common problems in clinical data mining of traditional Chinese medicine prescriptions].

Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica·2023
Same author

Preventive online and offline health management intervention in polycystic ovary syndrome.

World journal of clinical cases·2022
Same author

[Moxibustion on plaque psoriasis of blood stasis: a randomized controlled trial].

Zhongguo zhen jiu = Chinese acupuncture & moxibustion·2021
Same author

Neural networks and the anti-inflammatory effect of transcutaneous auricular vagus nerve stimulation in depression.

Journal of neuroinflammation·2020
Same author

Role of inflammation in depression relapse.

Journal of neuroinflammation·2019
Same author

Resting-state mapping of neural signatures of vulnerability to depression relapse.

Journal of affective disorders·2019

Related Experiment Video

Updated: Jun 7, 2025

Author Spotlight: Development and Evaluation of a Compound Acne Rodent Model Using C. acnes and Oleic Acid
03:10

Author Spotlight: Development and Evaluation of a Compound Acne Rodent Model Using C. acnes and Oleic Acid

Published on: November 1, 2024

2.3K

A Rat Model of Compound Acne.

Lin Chen1, Qi Jin1, Tian Xia2

  • 1Beijing Hospital of Traditional Chinese Medicine, Capital Medical University; School of Traditional Chinese Medicine, Beijing University of Chinese Medicine.

Journal of Visualized Experiments : Jove
|November 18, 2024
PubMed
Summary

This study successfully created a new rodent model for acne vulgaris by combining oleic acid and Cutibacterium acnes (C. acnes) to induce inflammation, offering a valuable tool for acne research.

More Related Videos

Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate DMBA-TPA
04:12

Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate DMBA-TPA

Published on: December 19, 2019

14.2K
Resolving Water, Proteins, and Lipids from In Vivo Confocal Raman Spectra of Stratum Corneum through a Chemometric Approach
09:32

Resolving Water, Proteins, and Lipids from In Vivo Confocal Raman Spectra of Stratum Corneum through a Chemometric Approach

Published on: September 26, 2019

7.1K

Related Experiment Videos

Last Updated: Jun 7, 2025

Author Spotlight: Development and Evaluation of a Compound Acne Rodent Model Using C. acnes and Oleic Acid
03:10

Author Spotlight: Development and Evaluation of a Compound Acne Rodent Model Using C. acnes and Oleic Acid

Published on: November 1, 2024

2.3K
Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate DMBA-TPA
04:12

Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate DMBA-TPA

Published on: December 19, 2019

14.2K
Resolving Water, Proteins, and Lipids from In Vivo Confocal Raman Spectra of Stratum Corneum through a Chemometric Approach
09:32

Resolving Water, Proteins, and Lipids from In Vivo Confocal Raman Spectra of Stratum Corneum through a Chemometric Approach

Published on: September 26, 2019

7.1K

Area of Science:

  • Dermatology
  • Microbiology
  • Animal Models

Background:

  • Acne vulgaris is a common skin condition.
  • Existing models do not fully replicate acne's complexity.

Purpose of the Study:

  • To establish a novel compound rodent model for acne vulgaris.
  • To simulate key aspects of acne inflammation using oleic acid and C. acnes.

Main Methods:

  • Rats were divided into four groups: control, oleic acid (OA) only, Cutibacterium acnes (C. acnes) only, and combined OA + C. acnes.
  • Oleic acid mimicked sebum production, while C. acnes injection induced bacterial inflammation.
  • Ear thickness, gross observation, histology, and immunohistochemistry (TNF-α) were used to assess inflammation.

Main Results:

  • The combined OA + C. acnes group showed significant ear thickening, induration, erythema, comedones, papules, and abscesses.
  • Histopathology revealed hyperkeratinization, follicular infundibulum expansion, and inflammatory cell infiltration.
  • Immunohistochemistry confirmed elevated tumor necrosis factor-alpha (TNF-α) levels in inflamed ears.

Conclusions:

  • A compound rodent model effectively simulates acne vulgaris inflammation.
  • This model provides a robust platform for studying acne pathogenesis and testing therapeutics.