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Other Disorders of Digestive System01:30

Other Disorders of Digestive System

The gastrointestinal tract is susceptible to various disorders. If the lower esophageal sphincter is damaged, stomach acid can flow back into the esophagus, causing irritation and inflammation of the lining. This condition is called gastroesophageal reflux disease (known as heartburn) and may cause chest pain and difficulty swallowing. In the stomach, prolonged use of nonsteroidal anti-inflammatory drugs like aspirin, chronic alcohol consumption, bacterial infections such as Helicobacter...
Gastroesophageal Reflux Disease I: Meaning and Pathophysiology01:29

Gastroesophageal Reflux Disease I: Meaning and Pathophysiology

Gastroesophageal Reflux Disease (GERD) involves the recurrent backflow of the stomach or duodenal contents into the esophagus, leading to troublesome symptoms and potential esophageal mucosal damage. Although GERD is often referred to as a disease, it is more accurately described as a syndrome, as it encompasses a range of symptoms and complications rather than a singular pathological entity, impacting a large number of individuals as the most prevalent upper gastrointestinal problem. Roughly...
Gastroesophageal Reflux Disease01:25

Gastroesophageal Reflux Disease

Gastroesophageal reflux disease (GERD) is the backward flow of stomach contents (acid, pepsin, or bile) into the esophagus, causing mucosal inflammation known as esophagitis. It results from failure of antireflux mechanisms, mainly the lower esophageal sphincter (LES), influenced by mechanical and physiological factors.Etiology and Risk FactorsGERD develops when LES function is weakened or when intra-abdominal pressure increases. Risk factors include aging, obesity, and sliding hiatal hernia,...
What is Monogastric Digestion?01:50

What is Monogastric Digestion?

The human body contains a monogastric digestive system. In a monogastric digestive system, the stomach only contains one chamber in which it digests food. Several other animal species also have monogastric digestive systems, including pigs, horses, dogs, and birds. This chapter, however, focuses on the human digestive system.
Hiatal Hernia01:25

Hiatal Hernia

A hiatal hernia is the abnormal protrusion of the stomach or other abdominal organs through the esophageal hiatus of the diaphragm into the thoracic cavity.Normally, the gastroesophageal junction (GEJ) lies below the diaphragm and is supported by the phrenoesophageal membrane, the diaphragmatic crura, and connective tissues. Weakening of these structures—due to aging, congenital defects like a short esophagus, or increased intra-abdominal pressure from coughing, obesity, pregnancy, or heavy...
Gastritis-II: Pathophysiology01:17

Gastritis-II: Pathophysiology

Gastritis is marked by disruption of the mucosal barrier that usually protects the stomach tissue from digestive juices and manifests in acute and chronic forms.
In acute gastritis, the gastric mucosa becomes swollen and red and undergoes superficial erosion. Superficial ulceration may lead to bleeding.
In chronic gastritis, persistent or repeated insults lead to chronic inflammatory changes and, eventually, thinning or atrophy of the gastric tissue.
Gastritis can stem from various causes, each...

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Related Experiment Video

Updated: May 21, 2026

Phosphorus-31 Magnetic Resonance Spectroscopy: A Tool for Measuring In Vivo Mitochondrial Oxidative Phosphorylation Capacity in Human Skeletal Muscle
09:40

Phosphorus-31 Magnetic Resonance Spectroscopy: A Tool for Measuring In Vivo Mitochondrial Oxidative Phosphorylation Capacity in Human Skeletal Muscle

Published on: January 19, 2017

Indigestible mitochondria cause heartburn.

Roberta A Gottlieb1, Phyllis-Jean Linton

  • 1Donald P. Shiley BioScience Center, San Diego State University, San Diego, CA 92182, USA. robbieg@sciences.sdsu.edu

Cell Research
|June 20, 2012
PubMed
Summary

Impaired autophagic flux prevents the degradation of mitochondrial DNA, worsening heart inflammation during pressure overload. This accumulation triggers inflammatory responses via Toll-like receptor 9 (TLR9).

Area of Science:

  • Cardiovascular Biology
  • Immunology
  • Cellular Biology

Background:

  • Autophagic flux is crucial for cellular homeostasis, particularly in the heart.
  • Mitochondrial damage and dysfunction are implicated in various cardiovascular diseases.
  • Inflammation plays a significant role in the pathogenesis of heart conditions like pressure overload.

Purpose of the Study:

  • To investigate the role of lysosomal degradation of mitochondrial DNA in myocardial inflammation.
  • To elucidate the mechanisms linking impaired autophagic flux, mitochondrial DNA, and inflammatory responses in the heart.

Main Methods:

  • Utilized a mouse model with cardiac-specific deletion of lysosomal DNase II.
  • Subjected mice to pressure overload via aortic banding.

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  • Analyzed mitochondrial DNA accumulation, lysosomal integrity, and inflammatory cytokine production.
  • Main Results:

    • Cardiac-specific deletion of DNase II led to accumulation of mitochondrial DNA within lysosomes.
    • This accumulation exacerbated myocardial inflammation under pressure overload conditions.
    • Inflammatory cytokine production was dependent on Toll-like receptor 9 (TLR9) activation.

    Conclusions:

    • Failure to degrade mitochondrial DNA due to impaired autophagic flux contributes significantly to myocardial inflammation.
    • Lysosomal DNase II is essential for clearing mitochondrial DNA and preventing TLR9-mediated inflammatory responses in the heart.
    • Targeting autophagic flux and mitochondrial DNA clearance may offer therapeutic strategies for pressure overload-induced heart disease.