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What is the other name for vitamin A2? Uncovering 3-Dehydroretinol

3 min read

First identified in the 1940s, vitamin A2 has a distinct chemical structure and origin that sets it apart from its more common counterpart, vitamin A1. The other name for vitamin A2, a crucial piece of this biochemical puzzle, is 3-dehydroretinol. This lesser-known retinoid plays a unique role in the biology of certain species, particularly freshwater fish.

Quick Summary

Vitamin A2 is also known as 3-dehydroretinol and is primarily found in freshwater fish. This retinoid plays a unique role in adapting the vision of certain species to their environment. It differs structurally from vitamin A1 and is less biologically active in mammals.

Key Points

  • Other Name: Vitamin A2 is also known as 3-dehydroretinol or dehydroretinol.

  • Primary Source: The main dietary source of vitamin A2 is the liver of freshwater fish.

  • Structural Difference: It differs from vitamin A1 (retinol) by having an extra double bond in its molecular structure, which affects its light absorption.

  • Role in Vision: Vitamin A2 forms porphyropsin, a visual pigment that helps certain aquatic species see more effectively in their specific watery environments.

  • Lower Activity in Mammals: In humans and other mammals, 3-dehydroretinol has significantly lower biological activity compared to retinol.

  • Evolutionary Adaptation: The ability to utilize vitamin A2 is an adaptation found in species that have evolved to thrive in different light conditions, such as migratory fish.

In This Article

Delving into 3-Dehydroretinol: A Form of Vitamin A

While most people are familiar with vitamin A1, or retinol, few have heard of its close relative, vitamin A2. The primary other name for vitamin A2 is 3-dehydroretinol, a moniker derived from its specific chemical structure. While it performs similar functions related to vision and growth, its properties and biological activity differ significantly from vitamin A1, especially across different species.

The Discovery and Definition of Vitamin A2

Vitamin A2 was first identified in the livers of freshwater fish and characterized by its unique light absorption properties. Its structure contains an additional double bond in the β-ionone ring compared to retinol, which accounts for its different biochemical behavior and spectral properties. This structural variation means that organisms utilizing vitamin A2 have adapted to incorporate this retinoid into their visual systems.

Where is Vitamin A2 Found?

Unlike vitamin A1, which is abundant in a wide range of animal products, vitamin A2 is predominantly found in aquatic life. This specialization is a key adaptation for organisms living in specific environments.

  • Freshwater fish: A prime source of vitamin A2, including species like herring, salmon, and trout, although the concentration can vary seasonally and by species.
  • Amphibians: Many amphibians, particularly those that undergo metamorphosis from an aquatic larval stage, utilize a visual system adapted for vitamin A2.
  • Some marine species: While most marine life relies on vitamin A1, certain euryhaline (salt-tolerant) species that migrate between fresh and salt water may have a mixed visual pigment system incorporating both vitamin A1 and A2.

Functions of Vitamin A2 in the Body

The primary function of vitamin A2, like vitamin A1, is its role in vision. It forms a crucial part of visual pigments, the light-sensitive molecules found in the retina. Specifically, vitamin A2 is a precursor to 3,4-dehydroretinal, which combines with opsin proteins to form porphyropsin, a visual pigment found in many freshwater species.

This system allows these animals to see more effectively in the specific light spectrum of their aquatic environment, which can differ significantly from terrestrial environments. While human skin can biosynthesize a small amount of 3,4-dehydroretinol from vitamin A1, its biological activity is significantly lower in humans and other mammals.

Comparison Table: Vitamin A1 vs. Vitamin A2

Feature Vitamin A1 (Retinol) Vitamin A2 (3-Dehydroretinol)
Prevalence Dominant form in most terrestrial vertebrates, including humans. Prevalent in freshwater fish and some amphibians.
Chemical Structure Retinol with a saturated beta-ionone ring. Features an additional double bond in the beta-ionone ring.
Visual Pigment Forms rhodopsin, with peak sensitivity around 500 nm. Forms porphyropsin, which shifts peak sensitivity towards longer (redder) wavelengths.
Biological Activity The most biologically active form for mammals, essential for vision, immune function, and reproduction. Has approximately 40% of the biological activity of retinol in mammals and is less efficient for human use.
Primary Sources Liver, dairy products, eggs, fish, and provitamin carotenoids from plants. Found primarily in the livers of freshwater fish.

The Evolutionary Purpose of the Vitamin A1/A2 System

The ability to switch between vitamin A1-based and vitamin A2-based visual systems is a remarkable evolutionary adaptation. In species like migratory fish, this mechanism allows for better vision as they move between different light environments (marine vs. freshwater). This change in visual pigment allows for maximum light absorption in the prevalent light conditions, offering a significant survival advantage.

Conclusion: The Specialized Role of 3-Dehydroretinol

So, what is the other name for vitamin A2? It is 3-dehydroretinol, a unique retinoid with a specialized function within the biological world. While its role in human health is minimal compared to the more common vitamin A1, its existence highlights the incredible diversity of life's adaptations. For freshwater fish and other aquatic species, this specialized form of vitamin A is a vital component of their survival, enabling them to perceive light in the precise wavelengths necessary for their environment. It serves as a fascinating example of how subtle chemical changes can drive significant evolutionary advantages. For a deeper scientific dive into the topic, resources like PubChem offer detailed chemical information.

Frequently Asked Questions

The other name for vitamin A2 is 3-dehydroretinol.

Vitamin A2 is primarily found in the livers of freshwater fish, as well as in some amphibians.

Vitamin A2 has a slightly different chemical structure, including an extra double bond, which gives it different light absorption properties than vitamin A1.

No, vitamin A2 has considerably lower biological activity in humans and is not considered a significant part of the human diet. Humans primarily utilize vitamin A1 (retinol).

In freshwater fish and other aquatic species, vitamin A2 is used to create visual pigments (porphyropsins) that are adapted to the light spectrum of their watery environment.

While it's not a common metabolic pathway in mammals, studies on rats have shown that some conversion from vitamin A1 to A2 can occur, though it is not a significant process.

Retinoids are a class of chemical compounds that are derivatives of vitamin A. Both vitamin A1 and vitamin A2 are part of this class of compounds.

References

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Medical Disclaimer

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