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Is Glycogen Digestible by Humans? The Science of Animal Starch

4 min read

The human body is equipped with a suite of enzymes to break down various complex carbohydrates, which is why when you consume meat, any trace glycogen is easily digested. A common query is, 'is glycogen digestible by humans?' and the answer is definitively yes, thanks to the alpha-glycosidic bonds that our digestive system is designed to process.

Quick Summary

Humans can digest dietary glycogen from animal-based foods using enzymes like salivary and pancreatic amylase and a debranching enzyme. The process differs from the internal breakdown of stored glycogen.

Key Points

  • Digestible Carbohydrate: Glycogen is fully digestible by humans because our bodies produce the necessary enzymes to break its $\alpha$-(1→4) and $\alpha$-(1→6) glycosidic bonds.

  • Key Enzymes: Digestion involves salivary and pancreatic $\alpha$-amylase to handle the linear glucose chains, and a specialized debranching enzyme to cleave the branch points.

  • Source of Dietary Glycogen: The only source of dietary glycogen is animal products, as plants store their energy as starch.

  • Differs from Internal Glycogenolysis: The digestion of dietary glycogen is an external process in the gut, distinct from the body's internal mechanism (glycogenolysis) for mobilizing its own stored glycogen from the liver and muscles.

  • Absorption of Glucose: Once digested, the resulting glucose molecules are absorbed into the bloodstream from the small intestine, providing a usable energy source for the body's cells.

In This Article

What Is Glycogen?

Glycogen is a highly branched polysaccharide, or complex carbohydrate, that functions as the primary energy storage molecule in animals. It is often referred to as 'animal starch' because it serves the same storage purpose as starch does in plants. The molecule is composed of many thousands of glucose units linked together by $\alpha$-(1→4) glycosidic bonds in its linear chains and $\alpha$-(1→6) glycosidic bonds at its numerous branch points. This intricate, branched structure makes it a compact and readily accessible source of glucose for the body.

For humans, glycogen is primarily stored in two locations: the liver and the skeletal muscles. Liver glycogen is used to regulate blood glucose levels and is broken down during periods of fasting to supply energy to the brain and red blood cells. In contrast, muscle glycogen serves as a local fuel source, providing a quick burst of energy for the muscle cells themselves during physical activity.

How Do Humans Digest Glycogen?

Unlike indigestible fibers like cellulose, which have $\beta$-(1→4) glycosidic bonds that humans cannot break, glycogen and starch are digestible due to their $\alpha$-(1→4) and $\alpha$-(1→6) linkages. The process of digesting dietary glycogen begins in the mouth and continues through the gastrointestinal tract, involving several key enzymes.

The Role of Amylase

Digestion of complex carbohydrates like starch and glycogen starts in the mouth with salivary $\alpha$-amylase. This enzyme randomly cleaves the $\alpha$-(1→4) glycosidic bonds of the polysaccharide chains, breaking them down into smaller fragments called dextrins, maltose (a disaccharide), and maltotriose (a trisaccharide). The activity of salivary amylase is short-lived, as it is quickly inactivated by the highly acidic environment of the stomach.

The bulk of carbohydrate digestion occurs in the small intestine, where pancreatic $\alpha$-amylase is released from the pancreas. This enzyme continues the work of breaking down the $\alpha$-(1→4) linkages, further reducing the complex carbohydrates into smaller glucose chains and maltose. However, amylase alone cannot completely break down glycogen because it cannot cleave the $\alpha$-(1→6) branch points.

The Importance of the Debranching Enzyme

To fully digest a branched polysaccharide like glycogen, a specific enzyme known as the glycogen debranching enzyme is required. This enzyme has two functions:

  • Glucosyltransferase Activity: It transfers a block of three glucose residues from a side branch to the end of another, longer branch, leaving a single glucose residue at the branch point.
  • Glucosidase Activity: It then hydrolyzes the remaining single glucose unit, which is attached by an $\alpha$-(1→6) bond, releasing it as free glucose.

Through the combined action of amylase and the debranching enzyme, dietary glycogen is systematically disassembled into individual glucose units. These monosaccharides are then absorbed through the intestinal wall into the bloodstream to be used for energy or stored.

Dietary Glycogen vs. Stored Glycogen

It's important to distinguish between the digestion of dietary glycogen and the body's internal mobilization of its own glycogen stores, a process called glycogenolysis.

Digestion in the Gastrointestinal Tract

When humans consume animal products, such as meat, that contain glycogen, it enters the digestive system just like any other carbohydrate. As described above, enzymes from the saliva and pancreas break it down into absorbable glucose molecules. This is an external, enzymatic process that happens in the gastrointestinal tract and yields glucose that can be distributed throughout the body via the bloodstream.

Glycogenolysis in the Liver and Muscles

In contrast, glycogenolysis is an internal metabolic process for releasing stored glucose from within the body's cells. It involves different enzymes than external digestion, most notably glycogen phosphorylase, which cleaves the $\alpha$-(1→4) bonds and produces glucose-1-phosphate, and the debranching enzyme for the $\alpha$-(1→6) bonds.

Differences in glycogenolysis exist between the liver and muscle cells. Liver cells can convert glucose-6-phosphate into free glucose using the enzyme glucose-6-phosphatase, allowing it to be released into the bloodstream to raise blood sugar levels. Muscle cells, however, lack this enzyme, so the glucose-6-phosphate is used exclusively for energy production within the muscle cell and cannot be released into the general circulation.

Comparison: Dietary Glycogen Digestion vs. Internal Glycogenolysis

Feature Dietary Glycogen Digestion Internal Glycogenolysis (Liver)
Location Gastrointestinal (GI) tract Hepatocytes (liver cells)
Initiating Factor Consumption of animal products Low blood glucose (fasting)
Primary Enzymes $\alpha$-Amylase and Glycogen Debranching Enzyme Glycogen Phosphorylase and Glycogen Debranching Enzyme
Primary Product Free Glucose (absorbed into blood) Free Glucose (released into blood)
Purpose To extract nutrients from food To maintain blood glucose homeostasis
Speed Part of normal digestive process Rapid response to hormonal signals like glucagon

Conclusion

In summary, humans are fully capable of digesting glycogen consumed as part of an animal-based diet. Our digestive system uses a combination of salivary and pancreatic amylase to break down the linear parts of the glycogen polymer, with the glycogen debranching enzyme handling the complex $\alpha$-(1→6) branch points. This external digestive process releases glucose into the bloodstream, where it is utilized for energy or converted to the body's own storage form of glycogen. This mechanism is distinct from the body's internal process of glycogenolysis, which is controlled by different metabolic pathways to regulate blood sugar levels during fasting or exercise. For more information on complex carbohydrate metabolism, the National Center for Biotechnology Information provides valuable resources on biochemistry topics like glycogen metabolism in humans.(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802397/)

Frequently Asked Questions

Glycogen and starch are both complex carbohydrates made of glucose units, but glycogen is the energy storage form found in animals, while starch is the energy storage form found in plants. Glycogen is more highly branched than starch, which makes it more compact and readily accessible for rapid glucose release.

Once dietary glycogen is broken down into glucose molecules by digestive enzymes, these monosaccharides are absorbed through the intestinal wall into the bloodstream. From there, the glucose is transported to cells throughout the body to be used immediately for energy or converted back into glycogen for storage.

Humans cannot digest cellulose because our bodies lack the enzyme (cellulase) required to break its specific $\beta$-(1→4) glycosidic bonds. In contrast, our bodies produce the enzymes (amylase and debranching enzyme) needed to break the $\alpha$-(1→4) and $\alpha$-(1→6) bonds found in glycogen and starch.

The human body produces the necessary enzymes primarily in two locations. Salivary $\alpha$-amylase is produced in the salivary glands, while pancreatic $\alpha$-amylase and the debranching enzyme are released from the pancreas into the small intestine.

Yes, digesting dietary glycogen results in the absorption of glucose into the bloodstream, which will increase blood sugar levels. This process is part of normal carbohydrate metabolism and triggers the release of insulin to help cells absorb the glucose.

Dietary glycogen is consumed from food (animal products) and broken down externally in the digestive tract. The body's own glycogen stores are synthesized internally from excess glucose and are broken down internally (glycogenolysis) when blood sugar is low.

The main function of the debranching enzyme is to remove the $\alpha$-(1→6) glycosidic bonds at the branch points of glycogen. This is crucial because $\alpha$-amylase can only break the linear $\alpha$-(1→4) bonds, meaning digestion would stop without the debranching enzyme's action.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.