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Aquaculture: Vitamin B6

Requirements

Table 1 lists vitamin B6 requirements for various species.

Vitamin B6 is stable under acidic conditions but unstable under neutral and alkaline conditions, particularly when exposed to heat or light. Of the several vitamers, pyridoxine is far more stable than either pyridoxal or pyridoxamine. Pyridoxine is fairly stable to air and heat if protected from light and humidity and is stable in dry multivitamin premixes that contain no added trace elements. Pyridoxine is readily soluble in water (about 20 g per 100 ml) and is used in dried form as pyridoxine hydrochloride.

Table 1

Much of the vitamin B6 in foods is not biologically available because it occurs in complexed forms, which are poorly digested. Both niacin (as nicotinamide adenine dinucleotide phosphate, or NADP) and riboflavin (as flavin adenine dinucleotide,) are required for normal vitamin B6 metabolism.

A. Dietary Protein Level

It is stated frequently that salmonids, because of their carnivorous nature, logically have a high dietary vitamin B6 requirement in comparison with species with lower protein requirements (Woodward, 1994). To date there is no conclusive evidence to support such a statement. Estimated pyridoxine requirements that have been reported to maximize the weight gain in young fish of nonsalmonid species range from 0.2 mg to 1.1 mg pyridoxine per 100 g protein. Values for salmonids range from 0.5 mg to 0.77 mg pyridoxine per 100 g of protein. Due to the different diets and husbandry conditions it is very difficult to make meaningful comparisons among different requirement studies.

Recent work with tilapia (Shiau and Hsieh, 1997) suggests that the dietary protein level influences the dietary pyridoxine requirement. The dietary pyridoxine requirements for optimal alanine aminotransferase activity were 9.5 mg and 15 mg in a 28% and 36% protein diet, respectively. Growth in the lower protein diet, which was estimated to be below the optimal protein requirement, was not optimal, which confounded the requirement estimate. Theoretically, if the protein had a well balanced amino acid profile that was available to the fish, most of the amino acids would have been utilized for protein synthesis, possibly sparing the amount of vitamin B6 required for catabolism of the amino acids.

Increasing the dietary pyridoxine level from 5 to 50 ppm was found to enhance sea bream (Sparus autraus) growth, feed efficiency and protein efficiency ratio (Baker and Davies, 1995) in a high-protein diet but not a low-protein diet (24 g versus 15 g of protein per MJ GE). Increasing the dietary pyridoxine level improved the apparent net protein utilization at both the low and high dietary protein levels.

Other studies into this question have not shown any interaction between dietary protein level and pyridoxine requirement in fishes (Hardy et al., 1979). There was no interaction between dietary protein and pyridoxine level on weight gain or feed efficiency in juvenile shrimp (Penaeus japonicus) (Giri et al., 1997).

Other studies showed a dose-dependent effect of pyridoxine on plasma glucose concentration in sea bream (Sparus autraus) (Morris and Davies, 1995a). This was thought to be due to the role of vitamin B6 in glycogen metabolism.

B. Vitamin B6 Effect on Immunity

Reduced Vitamin B6 intake or deficiency has severely impaired immunity in experimental animals and humans. The role of vitamin B6 in fish immunity has not been be clearly shown (Blazer, 1992; Olivier, 1997).

Hardy et al. (1979) found that pyridoxine conferred nonspecific resistance to juvenile chinook salmon (Oncorhynchus tshawytscha) against V. anguillarum. Leith et al. (1989) did not find increasing dietary pyridoxine levels to enhance the immune function or disease resistance of chinook salmon.

Feed levels of vitamin B6 higher than the minimum dietary requirement did not enhance immune functions and disease resistance in Atlantic salmon (Salmo salar) (Waagbø et al., 1992; Albrektsen et al., 1995; Olivier, 1997).

 

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