CoQ

Coenzyme Q₁₀ (CoQ₁₀ ), also known as ubiquinone, is a naturally occurring biochemical cofactor (coenzyme) and an antioxidant produced by the human body. It can also be obtained from dietary sources, such as meat, fish, seed oils, vegetables, and dietary supplements. CoQ₁₀ is found in many organisms, including animals and bacteria.

CoQ₁₀ plays a role in mitochondrial oxidative phosphorylation, aiding in the production of adenosine triphosphate (ATP), which is involved in energy transfer within cells. The structure of CoQ₁₀ consists of a benzoquinone moiety and an isoprenoid side chain, with the "10" referring to the number of isoprenyl chemical subunits in its tail.

Although a ubiquitous molecule in human tissues, CoQ₁₀ is not a dietary nutrient and does not have a recommended intake level, and its use as a supplement is not approved in the United States for any health or anti-disease effect.

Biological functions

CoQ₁₀ is a component of the mitochondrial electron transport chain (ETC), where it plays a role in oxidative phosphorylation, a process required for the biosynthesis of adenosine triphosphate, the primary energy source of cells.

CoQ₁₀ is a lipophilic molecule that is located in all biological membranes of human body and serves as a component for the synthesis of ATP and is a life-sustaining cofactor for the three complexes ( complex I, complex II, and complex III) of the ETC in the mitochondria. CoQ₁₀ has a role in the transport of protons across lysosomal membranes to regulate pH in lysosome functions.

The mitochondrial oxidative phosphorylation process occurs in the inner mitochondrial membrane of eukaryotic cells. This membrane is highly folded into structures called cristae, which increase the surface area available for oxidative phosphorylation. CoQ₁₀ plays a role in this process as an essential cofactor of the ETC located in the inner mitochondrial membrane and serves the following functions:
* electron transport in the mitochondrial ETC, by shuttling electrons from mitochondrial complexes like nicotinamide adenine dinucleotide (NADH), ubiquinone reductase (complex I), and succinate ubiquinone reductase (complex II), the fatty acids and branched-chain amino acids oxidation (through flavin-linked dehydrogenases) to ubiquinol–cytochrome-c reductase (complex III) of the ETC: CoQ₁₀ participates in fatty acid and glucose metabolism by transferring electrons generated from the reduction of fatty acids and glucose to electron acceptors;
* antioxidant activity as a lipid-soluble antioxidant together with vitamin E, scavenging reactive oxygen species and protecting cells against oxidative stress, inhibiting the oxidation of proteins, DNA, and use of vitamin E.

Biochemistry

Coenzymes Q is a coenzyme family that is ubiquitous in animals and many Pseudomonadota, a group of gram-negative bacteria. The fact that the coenzyme is ubiquitous gives the origin of its other name, ubiquinone. In humans, the most common form of coenzymes Q is coenzyme Q₁₀, also called CoQ₁₀ () or ubiquinone-10.

Coenzyme Q₁₀ is a 1,4-benzoquinone, in which "Q" refers to the quinone chemical group and "10" refers to the number of isoprenyl chemical subunits (shown enclosed in brackets in the diagram) in its tail. In natural ubiquinones, there are from six to ten subunits in the tail, with humans having a tail of 10 isoprene units (50 carbon atoms) connected to its benzoquinone "head".

This family of fat-soluble substances is present in all respiring eukaryotic cells, primarily in the mitochondria. Ninety-five percent of the human body's energy is generated this way. Organs with the highest energy requirements—such as the heart, liver, and kidney—have the highest CoQ₁₀ concentrations.

There are three redox states of CoQ: fully oxidized (''ubi''quinone), ''semi''quinone (''ubisemi''quinone), and fully reduced ( ubiquinol). The capacity of this molecule to act as a two-electron carrier (moving between the quinone and quinol form) and a one-electron carrier (moving between the semiquinone and one of these other forms) is central to its role in the electron transport chain due to the iron–sulfur clusters that can only accept one electron at a time and as a free radical–scavenging antioxidant.

Deficiency

There are two major pathways of deficiency of CoQ₁₀ in humans: reduced biosynthesis, and increased use by the body. Biosynthesis is the major source of CoQ₁₀. Biosynthesis requires at least 15 genes, and mutations in any of them can cause CoQ deficiency. CoQ₁₀ levels also may be affected by other genetic defects (such as mutations of mitochondrial DNA, '' ETFDH'', '' APTX'', '' FXN'', and '' BRAF'', genes that are not directly related to the CoQ₁₀ biosynthetic process). Some of these, such as mutations in '' COQ6'', can lead to serious diseases such as steroid-resistant nephrotic syndrome with sensorineural deafness.

Assessment

Although CoQ₁₀ may be measured in blood plasma, these measurements reflect dietary intake rather than tissue status. Currently, most clinical centers measure CoQ₁₀ levels in cultured skin fibroblasts, muscle biopsies, and blood mononuclear cells. Culture fibroblasts can be used also to evaluate the rate of endogenous CoQ₁₀ biosynthesis, by measuring the uptake of ¹⁴C- labeled ''p''-hydroxybenzoate.

CoQ₁₀ is studied as an adjunctive therapy to reduce inflammation in periodontitis.

Statins

Although statins may reduce CoQ₁₀ in the blood it is unclear if they reduce CoQ₁₀ in muscle. Evidence does not support that supplementation improves statin side effects.

Chemical properties

The oxidized structure of CoQ₁₀ is shown below. The various kinds of coenzyme Q may be distinguished by the number of isoprenoid subunits in their side-chains. The most common coenzyme Q in human mitochondria is CoQ₁₀. Q refers to the quinone head and "10" refers to the number of isoprene repeats in the tail. The molecule below has three isoprenoid units and would be called Q₃.
:

In its pure state, it is an orange-colored lipophile powder and has no taste or odor.

Biosynthesis

Biosynthesis occurs in most human tissue. There are three major steps:
# Creation of the benzoquinone structure (using phenylalanine or tyrosine, via 4-hydroxybenzoate)
# Creation of the isoprene side chain (using acetyl-CoA)
# The joining or condensation of the above two structures

The initial two reactions occur in mitochondria, the endoplasmic reticulum, and peroxisomes, indicating multiple sites of synthesis in animal cells.

An important enzyme in this pathway is HMG-CoA reductase, usually a target for intervention in cardiovascular complications. The "statin" family of cholesterol-reducing medications inhibits HMG-CoA reductase. One possible side effect of statins is decreased production of CoQ₁₀, which may be connected to the development of myopathy and rhabdomyolysis. However, the role statins play in CoQ deficiency is controversial. Although statins reduce blood levels of CoQ, studies on the effects of muscle levels of CoQ are yet to come. CoQ supplementation also does not reduce side effects of statin medications.

Genes involved include '' PDSS1'', '' PDSS2'', '' COQ2'', and '' ADCK3'' (''COQ8'', ''CABC1'').

Organisms other than humans produce the benzoquinone and isoprene structures from somewhat different source chemicals. For example, the bacteria '' E. coli'' produces the former from chorismate and the latter from a non- mevalonate source. The common yeast '' S. cerevisiae'', however, derives the former from either chorismate or tyrosine and the latter from mevalonate. Most organisms share the common 4-hydroxybenzoate intermediate, yet again uses different steps to arrive at the "Q" structure.

Dietary supplement

Although neither a prescription drug nor an essential nutrient, CoQ₁₀ is commonly used as a dietary supplement with the intent to prevent or improve disease conditions, such as cardiovascular disorders. CoQ₁₀ is naturally produced by the body and plays a crucial role in cell growth and protection. Despite its significant role in the body, it is not used as a drug to treat any specific disease.

Nevertheless, CoQ₁₀ is widely available as an over-the-counter dietary supplement and is recommended by some healthcare professionals, despite a lack of definitive scientific evidence supporting these recommendations, especially when it comes to cardiovascular diseases.

Regulation and composition

CoQ₁₀ is not approved by the U.S. Food and Drug Administration (FDA) for the treatment of any medical condition. However, it is sold as a dietary supplement not subject to the same regulations as medicinal drugs, and is an ingredient in some cosmetics. The manufacture of CoQ₁₀ is not regulated, and different batches and brands may vary significantly.

Research

A 2014 Cochrane review found insufficient evidence to make a conclusion about its use for the prevention of heart disease. A 2016 Cochrane review concluded that CoQ₁₀ had no effect on blood pressure. A 2021 Cochrane review found "no convincing evidence to support or refute" the use of CoQ₁₀ for the treatment of heart failure.

A 2017 meta-analysis of people with heart failure taking 30–100 mg/d of CoQ₁₀ found a 31% lower mortality and increased exercise capacity, with no significant difference in the endpoints of left heart ejection fraction. A 2021 meta-analysis found that coenzyme Q10 was associated with a 31% lower all-cause mortality in HF patients. In a 2023 meta-analysis of older people, ubiquinone had evidence of a cardiovascular effect, but ubiquinol did not.

Although CoQ₁₀ has been studied as a potential remedy to treat purported muscle-related side effects of statin medications, the results were mixed. Although a 2018 meta-analysis concluded that there was preliminary evidence for oral CoQ₁₀ reducing statin-associated muscle symptoms, including muscle pain, muscle weakness, muscle cramps, and muscle tiredness, 2015 and 2024 meta-analysis found that CoQ₁₀ had no effect on statin myopathy.

CoQ₁₀ is studied as an adjunctive therapy to reduce inflammation in periodontitis.

Pharmacology

Absorption

CoQ₁₀ in the pure form is a crystalline powder insoluble in water. Absorption as a pharmacological substance follows the same process as that of lipids; the uptake mechanism appears to be similar to that of vitamin E, another lipid-soluble nutrient. This process in the human body involves secretion into the small intestine of pancreatic enzymes and bile, which facilitates emulsification and micelle formation required for absorption of lipophilic substances. Food intake (and the presence of lipids) stimulates bodily biliary excretion of bile acids and greatly enhances absorption of CoQ₁₀. Exogenous CoQ₁₀ is absorbed from the small intestine and is best absorbed if taken with a meal. Serum concentration of CoQ₁₀ in fed condition is higher than in fasting conditions.

Metabolism

CoQ₁₀ is metabolized in all tissues, with the metabolites phosphorylated in cells. CoQ10 is reduced to ubiquinol during or after absorption in the small intestine. It is absorbed by chylomicrons, and redistributed in the blood within lipoproteins. Its elimination occurs via biliary and fecal excretion.

Pharmacokinetics

Some reports have been published on the pharmacokinetics of CoQ₁₀. The plasma peak can be observed 6–8 hours after oral administration when taken as a pharmacological substance. In some studies, a second plasma peak was observed approximately 24 hours after administration, probably due to enterohepatic recycling and redistribution from the liver to circulation.

Deuterium-labeled crystalline CoQ₁₀ was used to investigate pharmacokinetics in humans to determine an elimination half-time of 33 hours.''''

Bioavailability

In contrast to the intake of CoQ₁₀ as a constituent of food, such as nuts or meat, from which CoQ₁₀ is normally absorbed, there is a concern about CoQ₁₀ bioavailability when it is taken as a dietary supplement. Bioavailability of CoQ₁₀ supplements may be reduced due to the lipophilic nature of its molecule and large molecular weight.

Reduction of particle size

Nanoparticles have been explored as a delivery system for various drugs, such as improving the oral bioavailability of drugs with poor absorption characteristics. However, this has not proved successful with CoQ₁₀, although reports have differed widely. The use of aqueous suspension of finely powdered CoQ₁₀ in pure water also reveals only a minor effect.

Water-solubility

Facilitating drug absorption by increasing its solubility in water is a common pharmaceutical strategy and also is successful for CoQ₁₀. Various approaches have been developed to achieve this goal, with many of them producing significantly better results over oil-based soft gel capsules despite the many attempts to optimize their composition. Examples of such approaches are use of the aqueous dispersion of solid CoQ₁₀ with the polymer tyloxapol, formulations based on various solubilising agents, such as hydrogenated lecithin, and complexation with cyclodextrins; among the latter, the complex with β-cyclodextrin has been found to have highly increased bioavailability and also is used in pharmaceutical and food industries for CoQ₁₀-fortification.

Adverse effects and precautions

Generally, oral CoQ₁₀ supplementation is well tolerated. The most common side effects are gastrointestinal symptoms (nausea, vomiting, appetite suppression, and abdominal pain), rashes, and headaches. Some adverse effects, largely gastrointestinal, are reported with intakes. Doses of 100–300 mg per day may induce insomnia or elevate liver enzymes. The observed safe level risk assessment method indicated that the evidence of safety is acceptable at intakes up to 1200 mg per day.

Caution should be observed in the use of CoQ₁₀ supplementation in people with bile duct obstruction and during pregnancy or breastfeeding.

Potential drug interactions

CoQ₁₀ taken as a pharmacological substance has potential to inhibit the effects of theophylline as well as the anticoagulant warfarin; CoQ₁₀ may interfere with warfarin's actions by interacting with cytochrome p450 enzymes thereby reducing the INR, a measure of blood clotting. The structure of CoQ₁₀ is similar to that of vitamin K, which competes with and counteracts warfarin's anticoagulation effects. CoQ₁₀ is not recommended in people taking warfarin due to the increased risk of clotting.

Dietary concentrations

Detailed reviews on occurrence of CoQ₁₀ and dietary intake were published in 2010. Besides the endogenous synthesis within organisms, CoQ₁₀ also is supplied by various foods. CoQ₁₀ concentrations in various foods are:

Vegetable oils, meat, and fish are rich in CoQ₁₀. Dairy products are much poorer sources of CoQ₁₀ than animal tissues. Among vegetables, broccoli and cauliflower are good sources of CoQ₁₀. Most fruits and berries are poor sources of CoQ₁₀, except avocados, which have relatively high oil and CoQ₁₀ content.

Intake

In the developed world, the estimated daily intake of CoQ₁₀ has been determined at 3–6 mg per day, derived primarily from meat.

South Koreans have an estimated average daily CoQ (Q₉ + Q₁₀) intake of 11.6 mg/d, derived primarily from kimchi.

Effect of heat and processing

Cooking by frying reduces CoQ₁₀ content by 14–32%.

History

In 1950, a small amount of CoQ₁₀ was isolated from the lining of a horse's gut, a compound initially called ''substance SA'', but later deemed to be quinone found in many animal tissues. In 1957, the same compound was isolated from mitochondrial membranes of beef heart, with research showing that it transported electrons within mitochondria. It was called ''Q-275'' as a quinone. The Q-275/substance SA was later renamed ''ubiquinone'' as it was a ''ubiquitous'' quinone found in all animal tissues. In 1958, its full chemical structure was reported. Ubiquinone was later called either ''mitoquinone'' or ''coenzyme Q'' due to its participation to the mitochondrial electron transport chain. In 1966, a study reported that reduced CoQ₆ was an effective antioxidant in cells.

See also

* Idebenone – synthetic analog with reduced oxidant-generating properties
* Mitoquinone mesylate – synthetic analog with improved mitochondrial permeability

References

{{DISPLAYTITLE:Coenzyme Q₁₀

Antioxidants
1,4-Benzoquinones
Cellular respiration
Coenzymes
Glycolysis
Meroterpenoids
Phenol ethers
Polyenes