Influence of dietary supplementation on serum vitamin A and D concentrations and their seasonal variation in horses Markku Saastamoinen and Johanna Juusela Saastamoinen, M. T. & Juusela, J. 1992, Influence of dietary supplementation on serum vitamin A and D concentrations and their seasonal variation in horses. Agric. Sei. Finl. 1:477-482. (Agric, Res. Centre ofFinland, Equine Res. Sta., SF-32100 Ypäjä, Finland.) An experiment involving 40 adult trotters and saddle horses was conducted during a period of one year in order to investigate the influence of vitamin A (retinol) and D (25-(OH)D) supplementation on serum vitamin concentrations and the seasonal vari- ation of the serum concentrations of these vitamins. Vitamin supplementation was started either at the beginning or in the middle of the indoor (winter) feeding period. Supplementation lasted from the beginning of Septemberor January to the end ofMay. According to the results, neither the dietary vitamin supplementation nor the length of the grazing period had any consistent effect on the serum vitamin concentrations. Neither was there any systematic seasonal variation in the serum retinol and 25-hydro- xyvitamin D levels. Key words: blood serum, equine, fat-soluble vitamins Introduction Fresh grass and hay are the most important sources ofvitaminA (retinol) for horses (e.g., Fonnesbeck and Symons 1967). Vitamin D 3 is synthetized in the skin (Webb and Holick 1988). The synthesis of vitamin D 3 in the skin depends on season of the year, geographical latitude and intensity of sunlight (Nutrition Reviews 1989). During the winter season the supply of fat-sol- uble vitamins may be inadequate. The vitamin con- centrations of the most common combination of feeds used in horse feeding often decrease due to a long storage time. The synthesis of vitamin D 3 in the skin during the wintertime is minorbecause of the short day and the small amount of sunshine. Different chemical forms of blood vitamin A and D concentrations in horses have been determined in many previous studies. However, feed intake and the intake of vitamins from the basal feed have so far been poorly documented. The aim of this study was to investigate the in- fluence of vitamin A (retinol) and D (25-(OH)D) supplementation on the serum vitamin concentra- tions in horses during the different seasons of the year and the seasonal variationof serum concentra- tions of these vitamins. 477 Agric. Sei. Flnl. 1 (1992) https://www.c-info.fi/en/info/?token=KUtH9Bnr2SCbd0df.nyKPWVbyLy26WrRtWWtF5w.xRIWps-ETenKmitLB7OzxOsADcDHen2naeQ-I2gp-5skltfHC0RJfnIT3Ui1gPZxqaydXkG-6ISRp03AjOgs1XrQotIBgLBJATbailH8UIiHRKcyQ-JeinU7MIMjDliyzGsChE3eX5kavidbKsC5S-sDe0pos2ljljE8r3tyZrrjy0bfNAym6WJwx08NPjqh9WAjR-LQa2U48tT7bL9t9e3tIWD3QN3Fas6x32E1UHrL235J8BYzZjgrat1PAchrXB1yLNFTnhOX9wKLKck5RRf7cUH2eUZ29HXG0sTd Material and methods Horses Sixteen adult half-bred saddle horses (13 geldings, 3 mares) and 24 Finnhorses (17 geldings, 5 mares, 2 stallions) were used in the trial. Of the Finnhorses, one half were trotters and the other half riding horses. The age of the horses ranged between 5 and 17 years. The horses were exercised 1 to 2 h during the indoor feeding period. The trotters were trained for harness races, and the riding horses ofboth breeds in dressage and jumping mainly in a riding house. The half-bred saddle horses took part in regional riding competitions during the experiment. Of the Finnhorses, 7 riding horses competed in regional or national riding competitions and 8 trotters tookpart in national races. During the trial the weight of the horses was recorded every two months, and the state of their health was observed regularly. Basal feeding and vitamin supplementation In the summer, the horses were not exercised and were kept out on the pasture. The average length of the grazing period per horse was 37 days (s.d 26). During the indoor feeding period the the basal diet consisted of dried, timothy-dominated hay and oats. Small amounts (200-300 g) of either wheat bran or molassed sugar beet pulp were fed in addi- tion. The diet was balanced to meet the nutritional requirements of horses engaged in moderate work, and the feeds were dosed according to exercise, body weight and body condition. The horses were also given 50 g per day a calcium-rich mineral mixture (Ca;P= 3.5:1) which included supplement- al vitamin D 3 (40 000 ky/kg). The horses were devided into 3 vitamin sup- plementation groups (10 horses in each group), while 10 horses were controls. The daily vitamin dose was given orally, by adding it to the drinking water, in the form of a ADE-vitamin solution, a different solution for each supplemented group. The solutions were balanced for Vitamin E con- centration (60 mg vitamin E/ml) (Saastamoinen and Juusela 1992), and dosed individually accord- ing to the body weight (bwt) of the horse. Vitamin A and D 3 concentrations in the solutions were 3750, 2400 and 29301U, and 375,240 and 293 IU per ml, respectively. The daily supply of vitamins A and D 3 in the different supplemeted groups for a horse weighing 500 kg was 25550 and 4800 (LI, low), 60000 and 8000 (L2, medium), and 117800 and 13500 (L3, high) lU. Supplementation was started either at the begin- ning of the indoor (winter) feeding period (begin- ning of September) or in the middle ofit (beginning of January), and it was continued to the end ofMay. Thus, each supplemented group was subdivided into two sub-groups according to when the sup- plementation had started. Feed consumption was measured and feed samples (hay, oats, wheat bran, sugar beet pulp) were collected daily during the indoor feeding period, and the composition of the feeds was ana- lyzed by standard methods. The 13-caroteneand vit- amin D 3 content of the samples of hay, oats and pasture grass was determined at the laboratory of Farmos Group ltd (Turku, Finland) using high per- formance liquid chromatography (HPLC) (Schneider 1984). The determination of the vit- amin concentration in the hay and oats samples was made at thebeginning and end ofthe indoor feeding period. The vitamin content of the grass was deter- mined from one sample during the summer. A detailed description of the feeds, feeding man- agement and vitamin supplementation is given by Saastamoinen and Juusela (1992). Blood sampling and chemical analysis Blood samples were taken at rest (at 8.00 a.m.) from the jugular vein into evacuated blood collection tubes. Samples were taken on the Ist of June, Sep- tember, December and March, and at the end of the 478 Agric. Sei. Finl. 1 (1992) experimental period on the 31st of May. The samples were protected from light by covering the tubes with aluminiumfoil, and then stored at -60°C. The serum vitamin A (retinol) content (ng/ml) was determined using high performance liquid chromatography (HPLC) (Catignoni and Bieri 1983). Vitamin D (25-OH-vitamin-D) was deter- mined (ng/ml) by competitive protein-binding assay (PETTIFOR et al. 1976). The determinations were made in a clinical laboratory (Yhtyneet Labo- ratoriot Oy, Helsinki, Finland). The coefficients of infra- and inter-assay vari- ation were 3.4 % and 5.3 % for vitamin A, and 5.0 % and 7.0 % for vitamin D, respectively. Statistical methods The data were subjected to an analysis of variance. The statistical methods are described in more detail by Saastamoinen and Juusela (1992). Results and discussion The effect of the length of the grazing period or the dietary vitamin supplementation on the serum reti- nol and 25-OH-D levels (Table 1 and 2) was not found to be consistent or statistically significant (p<0.05). Neither was thereany consistent seasonal variation in the serum vitamin concentrations; the concentrations did not rise during the summertime. The mean concentrationof serum vitaminretinol was highest on the lowest supplementation level and lowest on the highest supplementation level (Table 1). The mean serum 25-hydroxyvitamin D concentration was also found to be highest on the lowest supplementation level (Table 2). The mean serum retinol concentration in the control horses (n=10) during the year’s period was 148.8 ng/ml (s.d 16.3 ng), and their mean serum 25-hydroxyvit- amin D content in the control horses was 7.05 ng/ml (s.d 0.79 ng). The mean concentrations for all the horses (n=4o) were 162.2 ng/ml (s.d 22.3 ng) and 6.45 ng/ml (s.d 0.70 ng), respectively. Table 1. Serum vitamin A concentrations (± s.d.) on different sampling dates and supplemental levels when supplementation was started either in the beginning (A) or middle (B) of the indoor feeding period (ng/ml) (n=s in each group). June September December March May A BABABABAB C 138.1 157.0 148.4 132.4 143.2 155.8 160.5 162.8 135.2 154.2 s.d 20.5 28.3 18.9 32.2 31.5 12.7 23.7 26.8 4.2 4.0 LI 165.0 163.9 159.3 176.5 181.7 154.2 194.3 171.9 202.9 171.3 s.d 15.9 12.9 20.4 18.9 13.8 2.9 3.7 11.3 5.7 11.3 L 2 147.3 150.1 141.5 151.9 175.9 178.8 171.9 162.8 186.2 173.6 s.d 25.2 22.7 17.9 48.7 56.7 11.4 31.5 14.4 11.8 14.4 L 3 150.7 163.3 154.2 155.9 162.8 163.9 171.3 174.8 150.1 171.3 s.d 19.7 47.3 5.1 44.1 13.8 27.6 11.3 18.9 14.7 18.9 M 150.3 158.7 150.7 154.2 165.9 163.2 174.5 168.1 168.6 167.6 s.d 21.3 27.5 16.8 26.7 34.6 36.2 22.7 15.9 37,8 19,0 LI, L 2 and L 3 are the supplementation groups (low, medium, high; see Material and methods C =control group; M =mean for all horses (n =20 per starting group) 479 Agric. Sei. Fint. 1 (1992) Table 2. Serum vitamin D concentrations (± s.d.) at different sampling dates and supplemental levels when supplementation was started either in the beginning (A) or middle (B) of the indoor feeding period (ng/ml)(n=s in each group). June September December March May ABABABABAB C 7.32 6.55 7.33 6.50 5.90 6.15 9.00 8.54 6,85 6.30 s.d 2.13 0.04 2,09 0.42 1.49 1.05 0.44 1.52 0.74 1.92 LI 7.05 5.91 5.94 4.34 4.73 4.18 7.92 8,15 6.15 7.54 s.d 0.57 0.07 1.22 0.78 0.05 0.48 0.34 0.74 1.09 0.34 L 2 5.78 6.42 7.65 5.73 5.52 7.46 7.08 7.85 5.23 5.38 s.d 1.18 1,37 0.48 1.68 1.45 0.42 0.34 0.44 0.34 0.39 L 3 6.32 7.12 5.89 5.37 5.66 5.58 7.62 6.77 5.23 5.77 s.d 1.47 0.22 1.54 1.25 2.07 0.81 0.69 1.00 0.44 0.39 M 6,62 6.50 6.70 5.48 5.45 5.87 7.90 7.83 5.87 6.25 s.d 1.47 0.83 1.57 1.31 1.42 1.36 0.84 1.15 0.97' 1.25 LI, L 2 and L 3 are the supplementation groups (low, medium, high; see Material and methdos) C =control group; M =mean for all horses (n =20 per starting group) The beta-carotene content of fresh pasture grass was 300 mg/kg DM (250-350 mg; n=4) and that of dried hay 13.3 mg/kg DM (5.0-20.0 mg; n=4). These were lower than reported for good quality hay and fresh grass in Finland (Salo et al. 1982). The change in the vitamincontent of the basal feeds during storage was minimal. Vitamin D2, which can be found in sun-driedroughages (McDonald et al, 1988), was not found in measurable amounts in the hay, which had been dried mainly artifically to ensure the best hygienic quality. The daily vitamin A intake during the grazing season could be estimated to be about 150000IU on the basis of the average DM intake capacity of 2V2 % of body weight (NRC 1989). The intake of vit- amin A from hay during the indoor feeding period was about 40000 IU per day. Thus, the total daily vitamin A intake for a 500 kg horse was 40000 IU in the control group and 65550,100000 and 157800 IU in the various supplementation groups. The daily vitamin A supply per each kg of feed dry matter fed was approximately 4300 IU for the con- trol horses, and 7050, 10750 and 17000 IU for the three supplemented groups. NRC (1989) recom- mends a vitamin A intake of 22000 lU/day for horses (500 kg) engaged in moderate work, equi- valent to 2140 IU/kg offeed (90% dry matter basis). Since there were no measurable amounts of vit- amin D in the hay, it was not possible to estimate the total vitamin D intake. However, the sup- plementation alone exceeded the current recom- mendations of NRC (1989) for daily vitamin D intake. Probably because the intake of vitamin A from the lowest supplementation level and the basal feeds and pasture was more than adequate for adult horses as compared to NRC (1989) norms, no in- fluence due to the supplementation and the season could be observed. Also the small data set and, the consequently high individual variation may have influenced the results. No harmfull effects due to the high intake of vitamin A could be observed. It may be expected that the excess ofvitaminA was stored in the liver (McDonald et al. 1988). 480 Agric. Sei. Fini. 1 (1992) Abrams (1979) and Sklan and Donoghue (1982) have reported that blood retinol increases with increasing dietary levels. FONNESBECK and Simons (1967) found differences in carotene util- ization by horses between different forage species. Also the base solution in the vitamin mixture has been reported to influence the utilization ofvitamin A (Bjondahl and Virkki 1977); the best utiliza- tion was reported for a vitaminmixture with xylitol as a base solution. In the present study mixtures with xylitol as a base solution were used. Mäenpää et al. (1987) found seasonal variation in the blood retinol concentrations of horses in training, whereas BUTLER and Blackmore (1982) did not. Seasonal variation has also been found in pregnant mares and in foals (Garton et al. 1964; Mäenpääetal. 1988 a and 1988b). The serum retinol level reported by Mäenpää et al. (1987) was 191 ng/ml in the winter and 208 ng/ml in the summer for Finnish trotters. BUTLER and Blackmore (1982) have reported an average concentration of 165 ng/ml in Thoroughbreds. Ab- rams (1979) observed slightly higher concentra- tions, i.e., 207.4 to 241.2 ng/ml in racing Thorough- breds. The blood retinol concentrations in brood mares have been found to range between 163 and 340 ng/ml (Stowe 1982, Mäenpää 1988 a and 1988b). The serum retinol concentrations given in the present study are thus somewhat lower than those reported previously. Mäenpää et al. (1987, 1988a) found seasonal variation also in serum 25-hydroxyvitamin D con- centrations. The concentrations of 25-hydroxyvit- amin D e.g. in Finnhorse mares were 4.20 ng/ml in the winter and 6.20 ng/ml in the summer (MÄEN- PÄÄ et ai. 1988a). The findings of the present study agree with those figures. It may be suggested that blood retinol levels alone can not be used as a basis for intake recom- mendations of vitamin A. According to Cuncha (1980) and Mäenpää et al. (1988 a) the blood vitamin A level is not a good indicator of the vit- amin A status of the horse. However, abnormally low intakes of vitamin A have been found to pro- duce alterations in total vitaminA concentrations in blood plasma (Donoghue et al. 1981). The findings of this study further showed that the serum 25-hydroxyvitamin D concentrations did not respond the dietary vitamin D intake or the grazing (amount of sunshine), and, thus, cannot be con- sidered in the determining vitamin D status and requirements of a horse. According to MÄENPÄÄ et al. (1988a), it is difficult to study the vitamin D status ofhorses due to the very low serum levels of 25-hydroxyvitamin D. Shorafa et al. (1979) have reported that dietary vitamin D is not needed by growing ponies when sunlight is abundant. The serum retinol and 25-hydroxyvitamin D con- centrations were higher in the half-bred saddle horses than in theFinnhorses throughout the experi- ment (p