Jove
Visualize
Contact Us

Related Concept Videos

Hypothalamic-Pituitary Axis01:37

Hypothalamic-Pituitary Axis

65.8K
The response to stress—be it physical or psychological, acute or chronic—involves activation of the Hypothalamic-Pituitary-Adrenal (HPA) axis. The HPA axis is part of the neuroendocrine system because it involves both neuronal and hormonal communication. Its function is to regulate homeostatic systems—metabolic, cardiovascular, and immune—providing the necessary means to respond to a stressor.
65.8K
Regulation of Food Intake01:30

Regulation of Food Intake

2.3K
Short-term regulation of food intake primarily involves neural signals from the gastrointestinal (GI) tract, blood nutrient levels, and GI tract hormones. Communication between the gut and brain via vagal nerve fibers plays a significant role in evaluating the contents of the gut. Clinical studies have shown that protein ingestion produces a more prolonged response in these nerve fibers compared to an equivalent amount of glucose. Additionally, the activation of stretch receptors caused by GI...
2.3K
Regulation of Water Intake01:25

Regulation of Water Intake

2.6K
Osmolality refers to the number of solute particles per kilogram of solvent in a solution. Plasma osmolality specifically indicates the total number of solute particles per kilogram of water in blood plasma. This value reflects the body's hydration status and is tightly regulated through mechanisms controlling water intake and output. While water consumption is a conscious decision, the body has intrinsic regulatory systems to maintain fluid balance. Dehydration, a state of water deficit...
2.6K
Perpendicular-Axis Theorem01:16

Perpendicular-Axis Theorem

4.5K
The perpendicular-axis theorem states that the moment of inertia of a planar object about an axis perpendicular to its plane is equal to the sum of the moments of inertia about two mutually perpendicular concurrent axes lying in the plane of the body.
Consider a circular disc of mass M and radius R lying along an x-y plane. The origin lies at the center of the disc, and the z-axis is perpendicular to the disc's plane. All three axes coincide at the disc's center. The moment of inertia of this...
4.5K
Parallel-axis Theorem01:06

Parallel-axis Theorem

8.2K
The parallel-axis theorem provides a convenient and quick method of finding the moment of inertia of an object about an axis parallel to the axis passing through its center of mass. Consider a thin rod as an example. There is a striking similarity between the process of finding the moment of inertia of a thin rod about an axis through its middle, where the center of mass lies, and about an axis through its end using the conventional method. In the conventional method, the concept of linear mass...
8.2K
Internal Receptors01:31

Internal Receptors

74.3K
Many cellular signals are hydrophilic and therefore cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind to internal, or intracellular, receptors that reside within the cell. Many mammalian steroid hormones use this mechanism of cell signaling, as does nitric oxide (NO) gas.
74.3K

You might also read

Related Articles

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

Sort by
Same author

Nicotinic acetylcholine receptors and their role in ghrelin-producing cells.

Biochemical and biophysical research communications·2026
Same author

Unlocking Selenium Chemical Space via a Programmable Synthesis Platform Bearing Cannabinoid Receptor Recognition Motifs.

Journal of the American Chemical Society·2026
Same author

Aquaporin 9 regulates acetaldehyde uptake, alcohol-induced liver injury, and drinking behavior.

Alcohol, clinical & experimental research·2026
Same author

Monlunabant in adults with obesity and metabolic syndrome: Open-label extension of a phase 2a trial.

Diabetes, obesity & metabolism·2026
Same author

A double-blind, randomized, placebo-controlled, phase 2 trial examined the efficacy and safety of monlunabant in adults with diabetic kidney disease.

Kidney international·2026
Same author

Hepatic Aquaporin 8 Promotes Alcohol Consumption and Ameliorates Alcohol-Induced Liver Injury by Facilitating Acetaldehyde Excretion.

International journal of biological sciences·2026
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 Experiment Video

Updated: Jan 24, 2026

A Gut-on-a-Chip Model to Study the Gut Microbiome-Nervous System Axis
09:18

A Gut-on-a-Chip Model to Study the Gut Microbiome-Nervous System Axis

Published on: July 28, 2023

3.5K

Targeting Peripheral CB1 Receptors Reduces Ethanol Intake via a Gut-Brain Axis.

Grzegorz Godlewski1, Resat Cinar1, Nathan J Coffey1

  • 1Laboratory of Physiologic Studies, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892, USA.

Cell Metabolism
|May 21, 2019
PubMed
Summary
This summary is machine-generated.

Blocking peripheral cannabinoid-1 receptors (CB1R) reduces alcohol drinking by inhibiting ghrelin production and signaling. This suggests a new therapeutic target for alcoholism treatment.

More Related Videos

Manipulation of Rhythmic Food Intake in Mice Using a Custom-Made Feeding System
07:34

Manipulation of Rhythmic Food Intake in Mice Using a Custom-Made Feeding System

Published on: December 16, 2022

2.8K
Author Spotlight: Accessible M&M-Based Mouse Model for Investigating Binge Eating Disorder - Insights into Eating Behaviors, Anxiety, and Neural Mechanisms
05:15

Author Spotlight: Accessible M&M-Based Mouse Model for Investigating Binge Eating Disorder - Insights into Eating Behaviors, Anxiety, and Neural Mechanisms

Published on: January 10, 2025

1.7K

Related Experiment Videos

Last Updated: Jan 24, 2026

A Gut-on-a-Chip Model to Study the Gut Microbiome-Nervous System Axis
09:18

A Gut-on-a-Chip Model to Study the Gut Microbiome-Nervous System Axis

Published on: July 28, 2023

3.5K
Manipulation of Rhythmic Food Intake in Mice Using a Custom-Made Feeding System
07:34

Manipulation of Rhythmic Food Intake in Mice Using a Custom-Made Feeding System

Published on: December 16, 2022

2.8K
Author Spotlight: Accessible M&M-Based Mouse Model for Investigating Binge Eating Disorder - Insights into Eating Behaviors, Anxiety, and Neural Mechanisms
05:15

Author Spotlight: Accessible M&M-Based Mouse Model for Investigating Binge Eating Disorder - Insights into Eating Behaviors, Anxiety, and Neural Mechanisms

Published on: January 10, 2025

1.7K

Area of Science:

  • Neuroscience
  • Endocrinology
  • Pharmacology

Background:

  • Endocannabinoids acting on cannabinoid-1 receptors (CB1R) and ghrelin acting on its receptor (GHS-R1A) both promote alcohol-seeking behavior.
  • The interaction between these two signaling systems in the context of alcohol consumption has not been previously investigated.

Purpose of the Study:

  • To investigate the interaction between CB1R and GHS-R1A signaling pathways in regulating alcohol consumption.
  • To explore the therapeutic potential of targeting peripheral CB1R in treating alcoholism.

Main Methods:

  • Administration of a peripheral CB1R inverse agonist (JD5037) to wild-type mice and mice genetically modified to lack CB1R, ghrelin peptide, or GHS-R1A.
  • Measurement of ethanol intake and analysis of ghrelin precursor and active forms.
  • Investigation of fatty acid metabolism in gastric cells and the role of vagal afferents.

Main Results:

  • JD5037 significantly reduced ethanol drinking in wild-type mice but not in mice lacking CB1R, ghrelin, or GHS-R1A.
  • JD5037 treatment inhibited the formation of active octanoyl-ghrelin and reduced octanoyl-carnitine levels in gastric cells by increasing fatty acid β-oxidation.
  • Blocking gastric vagal afferents abolished the alcohol-drinking-reducing effects of both CB1R and GHS-R1A blockade.

Conclusions:

  • Peripheral CB1R blockade reduces alcohol consumption by inhibiting active ghrelin formation in gastric cells.
  • The observed effects are mediated through ghrelin signaling via gastric vagal afferents.
  • Peripheral CB1R blockade represents a potential therapeutic strategy for alcoholism.