Taurine content in various food sources
Taurine (2-aminoethanesulfonic acid) is a sulphur-containing compound characterized as an amino acid. The presence of a sulfonic group, as opposed to a carboxyl group in other amino acids, gives taurine a pKa value of 1.5 and it is the most acidic amino acid. It is an exclusively free amino acid, i.e. it is not incorporated into proteins, but still widely distributed in most body tissues.
Taurine was identified almost two centuries ago and was named after the ox,
In felines taurine is considered indispensable and dietary deficiency leads to several clinical problems, including retinal degeneration and developmental abnormalities . In humans it is regarded as a conditionally essential amino acid due to a limited ability to synthesize it [14, 15]. Taurine is now thought to play a more important role in human nutrition, and an increased dietary intake of taurine has been linked to several beneficial health outcomes in various diseases and medical conditions [16-18].
2. Taurine and nutrition
Estimates of dietary intake of taurine vary greatly. Although taurine content have been analysed in a variety of foods, it is usually excluded in food and nutrition data banks. Therefore, it is difficult to assess the dietary intake. A diet high in meat and especially seafood will provide a higher intake than a vegetarian diet which will provide very little taurine . Mean ± SE dietary intake of taurine of 58 ± 19.5 mg/d was reported in omnivores , while it was not detected in a vegan diet. Laidlaw et al.  analysed taurine content in foods and calculated a taurine intake of less than 200 mg/d for individuals consuming a diet high in meat.
2.1. Taurine biosynthesis
Taurine is the most abundant intracellular free amino acid in the human body, the average amount being approximately 560 mmol (70g). The main organs of distribution are the retina, along with white blood cells, platelets, spleen, heart, muscle and brain .
As a product in the metabolism of sulphur-containing amino acids, taurine can be synthesised from its precursors methionine and cysteine, as shown in figure 2. The first step of the synthesis is methionine’s reversible conversion to homocysteine by transmethylation and remethylation processes. Homocysteine can then be converted irreversibly to cysteine through the transsulfuration pathway catalyzed by cystathionine β-synthase and cystathionine γ-lyase . Cysteine is, in turn, the origin of several biologically important molecules, including glutathione, inorganic sulphur and taurine . Taurine can be synthesised from cysteine through several pathways, most commonly via cysteine sulfinic acid and hypotaurine, involving the enzymes cysteine dioxygenase (CDO) and cysteine sulfinic decarboxylase (CSAD) mainly present in the liver and brain. The activities of the enzymes involved, in particular the activity of CSAD, are both species and age dependent [25-27], being high in rodents and absent in cats. In addition, taurine synthesis is dependent on an adequate cysteine concentration, as production of glutathione is favoured when cysteine concentration is limited .
In humans the CSAD activity is low and the average daily synthesis of taurine ranges from 0.4 to 1.0 mmol (50-125mg). Excretion of taurine is very variable (0.22-1.85 mmol day-1) and affected by several factors such as genetics, age, gender, dietary intake, kidney function and health status . The taurine body pool size is however regulated by the kidneys through renal absorption by the proximal tubule [14, 26, 29, 30].
2.2. Dietary sources
Taurine is found in most meats used for human consumption, whereas plants including grains, legumes, fruits and vegetables are devoid or contain only negligible amounts . An exception is algae, mainly red algae (
Taurine concentration has been investigated in a wide range of food products and it varies substantially between different marine and non-marine food items [17, 33]. A comparison of taurine concentrations in various foods is presented in table 1 [21, 34-43]. It is evident that seafood, and especially molluscs are high in taurine. Taurine is a key osmolyte in marine molluscs  and the highest taurine concentrations are found in marine bivalves and univalves . Scallops and blue mussels are reported to have a respective taurine content of 827±15 and 510±12 mg per 100g raw muscle [21, 34]. In fact, the univalve abalone was already early in the last century 1918 exploited for preparation of taurine in large quantities .
There is also a tendency of taurine being more abundant in fish than in terrestrial animals. Taurine concentrations (mg per 100g raw fillets) of entire muscle of farmed Atlantic salmon (94 ± 16 mg), cod (120 ± 21 mg), saithe (162 ± 25 mg) and haddock (57 ± 6 mg) are reported to be intermediate . Taurine content varies greatly between white and red muscle both in fish, poultry and mammals, with significantly higher levels being present in red muscle [21, 39, 40, 43], probably due to the increased vascularisation of these tissues.
Several studies investigating the retention and losses of taurine during food processing and preparation have been conducted [34, 36, 47-49]. Results indicate that taurine is susceptible to leaching losses similar to or even more than other free amino acids. Data on the oxidative and heat stability of taurine in foods is scarce. In milk, taurine losses seemed to proceed with the same degradation rate as lysine due to browning reactions .
2.3. Taurine supplementation
Taurine is maybe most famous for being an ingredient that is added to energy drinks, the concentration being approximately 4.0 g/L. Its physiological effect has been debated, with manufacturers, backed by studies, claiming that taurine in combination with other active ingredients may improve cognitive and muscular performance [51, 52]. The safety of taurine intake has also been investigated, especially in conjunction with its use in energy drinks. The European Food Safety Authority (EFSA) have concluded that taurine do not present any safety concerns with the levels currently used in energy drinks. The no observable adverse effect level (NOAEL) was at least 1000 mg/kg bw/day for pathological and behavioural changes, being much higher than an extreme consumer would be exposed to . In their risk assessment, Shao and Hatchcock , found that absence of adverse effects was strong for taurine at supplemental intakes up to 3 g per day.
(mg/100g wet weight)
reported range ± SEM
|43 ± 8|||
|18 ± 3|||
|169 ± 37|||
|30 ± 7|||
|306 ± 69|||
|61 ± 11||[21, 38]|
|50 ± 11||[21, 38]|
|45 ± 4|||
|40 ± 13|||
|62,4 ± 12|||
|28 ± 13|||
|146 ± 5||[|
|120 ± 21||[34, 48]|
|162 ± 25|||
|57 ± 6|||
|201 ± 32|||
|94 ± 16|||
|388 ± 13|||
|356 ± 95|||
|220 ± 2|||
|510 ± 12|||
|655 ± 72|||
|520 ± 97||[21, 43]|
|827 ± 15|||
|396 ± 29|||
Another food item where taurine is supplemented is in infant formulas. This practice started in the early 1980s after recognizing that preterm infants fed infant formulas had lower urine and plasma concentrations than infants fed pooled human milk . The necessity of this supplementation remains disputed as clinical studies have not provided evidence of any clinical effects of growth and development in preterm or low birth weight infants . High concentrations of taurine in the developing brain , as well as results from various animal studies clearly indicate the importance of taurine in neurodevelopment [58, 59].
2.4. Taurine and associated health benefits
An increased dietary intake of taurine has been associated with multiple beneficial health outcomes. Epidemiological data and animal studies suggests that dietary intake of taurine has beneficial effects on cardiovascular disease (CVD) [33, 60-62]. Perhaps the best characterized attribution of taurine is the antihypertensive effect although there are still questions about the exact mechanisms of action [63-66]. A long term effect of hypertension is the development of hypertrophy of the left ventricle, in which Angiotensin II (Ang II) plays an important role. Several studies have shown that taurine reverses these actions of Ang II [67, 68]. Animal studies have also indicated that taurine may reduce insulin resistance [69, 70], but most of the clinical studies have failed to prove the beneficial role of taurine in insulin resistance and diabetic complications [71, 72]. Taurine have also been found to ameliorate alcoholic steatohepatitis [73-75] in rats. In addition, some evidence have been brought forward of a potential therapeutic use of taurine in nonalcoholic fatty liver disease . Despite taurine being linked to beneficial health outcomes in an increasing number of diseases and medical conditions, the number of studies is relatively small. The effects of taurine on cholesterol and CVD are most studied and documented.
3. Taurine and cholesterol metabolism
Perhaps the best studied function of taurine is its role in cholesterol metabolism. Cholesterol is metabolized and broken down to cholic acids, conjugated to taurine or glycine, and excreted in the bile .
3.1. Effects of taurine on circulating cholesterol levels
High blood cholesterol levels is the most pronounced risk factor for developing atherosclerosis, vascular inflammation and hardening of the arteries associated with excess cholesterol deposition in the vasculature. Taurine has generally been associated with a beneficial effect on blood cholesterol levels. Cholesterol is metabolized and broken down to cholic acids, conjugated to taurine or glycine, and excreted in the bile . The conjugation pattern varies considerably across species. In dog and rat bile acids are entirely conjugated to taurine, whereas rabbits have all their bile acids conjugated to glycine. Species where glycine-conjugated bile acids dominate have higher blood cholesterol levels and are more susceptible to dietary induced hypercholesterolemia, and based on these observations it was hypothesized that dietary taurine might counteract dietary induced increase in blood cholesterol .
3.1.1. Effects of taurine on cholesterol levels in mice
Several studies have investigated the effect of dietary intake of taurine on lipids in different mice strains. Six months administration of 1% taurine (w/v) to the drinking water given to C57BL7/6J mice fed a high-fat diet resulted in reduced serum LDL and VLDL cholesterol and increased serum HDL cholesterol . Similar results were obtained in a small study using the same mouse strain, where 1% taurine (w/w) added to a high cholesterol diet reduced serum triglycerides, total cholesterol and VLDL+LDL cholesterol levels already after 4 weeks treatment . Cholesterol-fed and streptozotocin (STZ)-induced diabetic male ICR mice were given a diet enriched with 2% cholesterol (w/w) and 0.5% cholate (w/w) for 10 weeks . In addition, mice received a daily dose of saline or taurine (50 or 100 mg/kg p.o.). Both taurine-treated groups had lower serum total and LDL cholesterol compared to the STZ/saline group.
In more extreme models such as apolipoprotein E-deficient (apoE-/-) mice fed a normal rodent chow supplemented with 2% taurine (w/w) for 12 weeks, serum VLDL, LDL and total cholesterol levels increased compared to mice without taurine supplementation . Similar results has been reported for extreme spontaneously hyperlipidemic mice (SHL; KOR-
3.1.2. Effects of taurine on cholesterol levels in rats
A large number of studies have investigated the effect of dietary taurine on dietary hypercholesterolemia in various rat models . Rats fed high-fat diets seem to be the model with most consistent antihypercholesterolemic effects of dietary taurine. Rats have a relatively low taurine content in skeletal muscles (10-25 mg/100 g muscle) [83, 84].
Rats are generally not suitable for pharmacologically cholesterol and lipoprotein studies due to their substantially different lipid profile compared to humans.
3.1.3. Effects of taurine on cholesterol levels in rabbits
Different rabbit strains have been used to investigate the effects of dietary taurine supplementation on dietary induced hypercholesterolemia [86, 97, 98]. The results from the administration of taurine to rabbits have been ambiguous. In
3.1.4. Effects of taurine on cholesterol levels in hamsters
Hamsters (Male Golden Syrian hamsters) have also been used as model for studying cholesterol metabolism. The rationale for this is that hamsters and humans have comparable blood cholesterol levels, hamsters use both taurine and glycine for bile acid conjugation and the lipoprotein profile in response to dietary cholesterol is comparable . When Male Golden Syrian hamsters were fed a normal chow supplemented with 0.05% cholesterol or a 10% coconut oil, high-fat diet (0.05% cholesterol) for two weeks, taurine dissolved in drinking water (1% w/v) reduced serum total cholesterol in chow- (15% reduction) as well as high-fat diet-fed (42% reduction) hamsters . A similar effect was observed for non-HDL (LDL+VLDL) cholesterol.
Recently, lipid metabolism has been closely studied in Male Golden Syrian Hamsters fed different diets with or without taurine for 4 weeks . The groups received a high fat diet (chow mixed with 7% butter [w/w] and 0.2% cholesterol [w/w]) and drinking water without or supplemented with either 0.35% or 0.7% taurine (w/v). Hamsters given taurine was smaller, had less visceral fat and smaller livers after 4 weeks. Both taurine concentrations resulted in significant lower serum triglycerides, total cholesterol, and LDL+VLVL cholesterol. Up-regulated gene expression of the low-density lipoprotein receptor and CYP7A1 genes, paralleled by increased faecal cholesterol and bile acid concentrations in the taurine treated hamsters, indicated that the taurine effect on the cholesterol and lipid profiles is due to increased cholesterol metabolism.
3.1.5. Effects of taurine on cholesterol levels in humans
Historically, taurine has been believed to decrease blood cholesterol levels in adults. Only a limited number of studies have investigated the effect of oral taurine supplementation on blood cholesterol or lipoprotein levels in humans and ambiguous results have arisen from these. Early studies found no effect on serum cholesterol after incidental treatment of patients with 1.5 to 3 g taurine/day for up to 2 months [77, 104, 105]. To our knowledge there has been no well-designed random controlled clinical trial assessing the dose-response effect of oral taurine supplementation on blood lipids in healthy humans. However, the effect of taurine in relation to development of CVD has been documented through a human clinical trial. Results of a 7 week human intervention trial revealed that supplementation with 0.4 g taurine/day in combination with omega-3 fatty acids (1 g EPA+DHA/day) significantly improved the lipid profiles by reducing serum total and LDL cholesterol levels compared to supplementation with omega-3 fatty acids alone . In another study the effects of oral supplementation with taurine (3 g/day) or placebo for 7 weeks was assessed in young obese healthy subjects . In this study, taurine had no effect on serum cholesterol, but triglycerides and bodyweight was significantly reduced compared to placebo effect. Finally, a daily 6 g taurine supplementation to human healthy volunteers receiving a cholesterol-inducing diet for 3 weeks attenuated the expected increase of serum total cholesterol and LDL-cholesterol, whereas serum VLDL-cholesterol and triglyceride levels compared to the control group . In insulin-dependent diabetes mellitus patients intake of taurine (1 g/day) reduced serum triglyceride levels, but no effect was observed on serum cholesterol . Finally, in a randomized, double-blinded, crossover intervention, overweight non-diabetic men given a daily dose of 1.5 g taurine or placebo, no effect was reported on blood lipids . In summary, results from oral taurine supplementation to humans are ambiguous, and further adequately designed interventions are warranted to further investigate the potential of taurine as a hypocholesterolemic agent.
4. Effects of taurine on atherogenesis/development of atherosclerosis
High blood cholesterol levels is the most pronounced risk factor for developing atherosclerosis, vascular inflammation and hardening of the arteries associated with excess cholesterol deposition in the vasculature. Apart from humans and monkeys, wild animals normally do not develop substantial atherosclerosis. There is however, an array of laboratory animal models in common use for studying the effects of pharmacological substances and dietary modifications on lesion formation. The effect of taurine has been investigated in several of these models.
4.1. Effects of taurine on atherosclerosis in mice
In the hyperlipidemic apoE-/- mice, taurine has been reported to delay atherogenesis by decreasing oxidized substances that cause inflammation, as well as increasing HDL-cholesterol . Also in apoE-/- mice fed a normal rodent chow supplemented with 2% taurine (w/w) for 12 weeks, formation of atherosclerotic lesions were significantly reduced . However this effect was independent of serum cholesterol as VLDL, LDL, and total cholesterol were increased.
Moreover, in spontaneously hyperlipidemic mice, taurine (1% w/v) provided through drinking water, was reported to suppress the development of lesion formation without affecting the levels of serum VLDL and LDL .
In our lab, apoE-/--mice were given Western diets (WD) containing 20% fat (w/w), 0.2% cholesterol (w/w) for 13 weeks . The mice received WD, WD supplemented with 0.5% taurine (w/w) or WD supplemented with 0.5% taurine (w/w) in combination with a daily dose of marine long-chain omega-3 polyunsaturated fatty acids (n-3 PUFA) recommend in the dietary guidelines for humans. In these studies, taurine did not affect serum cholesterol or triglyceride levels alone or combination with n-3 PUFA. This may indicate that a larger supplementary dose of taurine is needed to prevent dietary induced hypercholesterolemia in apoE-/--mice.
4.2. Effects of taurine on lipid lesion formation in rats
Rats are generally not a suitable animal model for atherosclerosis as they do not develop lesion deposits resembling the early phase of human atherogenesis. However, in a rat model of balloon induced vascular neointima formation, supplementation with taurine (3% in drinking water) from 2 days before the surgical procedure and 14 days after, reduced vascular smooth muscle cell proliferation . This key step in the initiation of atherogenesis was reduced by 28% compared to control fed rats. Taurine was located immunohistochemically mainly to the surface of the exposed media and adventitia of the injured carotid artery and higher levels were observed in the taurine treated rats. This corresponded to a lower vascular production of superoxide anion compared to the control animals. From these experiments it was concluded that the preventive effect of taurine towards neointima formation was attributable to anti-oxidative effects.
4.3. Effects of taurine on atherosclerosis in rabbits
The effect of dietary taurine on development of atherosclerosis has been investigated in different rabbit strains. Taurine has been indicated to prevent progression of atherosclerotic lesions in rabbits without affecting serum cholesterol in two different models. In New-Zealand white male rabbits given a diet containing 2% cholesterol (w/w), taurine added to the drinking water (0.1 or 0.5% w/v) for 14 weeks reduced the aortic deposition of fat . This so-called anti-atherosclerotic effect was only significant for the highest taurine dose tested. Recently, it was indicated that the taurine antiatherosclerotic effect was evident in these rabbits after only 4 weeks on the atherogenic diet .
4.4. Effects of taurine on atherosclerosis in humans
Results on the effects of dietary taurine in humans are mainly from prospective studies. It is evident that individuals with high urinary excretion of taurine and high dietary intake of food high in taurine in general have fewer incidences of cardiovascular diseases compared to individuals with low dietary intake of taurine . In addition, increased dietary intake of taurine either alone or in the combination with omega-3 fatty acids, has also been suggested to reduce MCP-1, an important risk factor of CVD . No further randomised clinical trials on the effects of dietary supplementation of taurine on CVD disease markers has been reported.
Taurine appears to be able to prevent hypercholesterolemia and hepatic steatosis induced by high-fat and high-cholesterol diets in most animal models. The major mechanism by which taurine lowers serum cholesterol levels is by increased utilization of cholesterol for bile acid synthesis. In mice, rats, and hamsters, dietary intake of taurine cause reduction in diet-induced serum cholesterol accompanied by enhanced mRNA expression and enzymatic activity of 7a-hydroxylase, the rate-limiting enzyme of bile acid synthesis. In normal diets taurine does not appear to modify serum and liver cholesterol levels.
Dietary supplementation with taurine is indicated to have cardiovascular benefits. The effect on atherosclerosis appears to be highly dose- and model-dependent. In animal experiments using high-fat diets to induce increased levels of lipids, taurine has been demonstrated to significantly alleviate atherosclerotic lesions. The effects of taurine appear to be related to increased degradation and excretion of cholesterol as bile in the feces and the most common feature is that taurine increases expression and activity of cholesterol 7α-hydroxylase. Only a few studies have evaluated the effects of taurine in human subjects.
From the available data it is not possible to conclude about the proposed antihyperlipidemic and antiatherosclerotic, therefore more basic and clinical research on the effects of taurine supplementation on hypercholesterolemic and atherosclerotic effects are warranted. Randomized clinical trials of dietary taurine and taurine sources may provide further knowledge about the potential hypocholesterolemic and antiatherogenic effects of long-term dietary taurine supplementation in healthy volunteers and humans with hyperlipidemia, metabolic syndrome and cardiovascular diseases.
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