Effects of Supplementing Brown Seaweed By-products in the Diet of  Holstein Cows during Transition on Ruminal Fermentation,  Growth Performance and Endocrine Responses

Z. S. Hong; E. J. Kim; Y. C. Jin; J. S. Lee; Y. J. Choi; H. G. Lee

doi:10.5713/ajas.15.0235

Anim Biosci > Volume 28(9); 2015 > Article

Hong, Kim, Jin, Lee, Choi, and Lee: Effects of Supplementing Brown Seaweed By-products in the Diet of Holstein Cows during Transition on Ruminal Fermentation, Growth Performance and Endocrine Responses

Article

Asian-Australasian Journal of Animal Sciences (AJAS) 2015; 28(9): 1296-1302.

https://doi.org/10.5713/ajas.15.0235

Effects of Supplementing Brown Seaweed By-products in the Diet of Holstein Cows during Transition on Ruminal Fermentation, Growth Performance and Endocrine Responses

Z. S. Hong^a, E. J. Kim^1,^a, Y. C. Jin², J. S. Lee², Y. J. Choi³, H. G. Lee^2,^*

¹Department of Animal Science, Kyungpook National University, Sangju 742-711, Korea.

²Department of Animal Science and Technology, Konkuk University, Seoul 140-701, Korea.

³Laboratory of Animal Cell Biotechnology, Department of Agricultural Biotechnology, Seoul National University, Seoul 151-742, Korea.

^*Corresponding Author: H. G. Lee.
Tel: +82-2-450-4387, Fax: +82-2-3436-0106, E-mail: hglee66@konkuk.ac.kr

Department of Animal Science and Technology, Tianjin Agricultural University, Tianjin 300384, China

^a These authors contributed equally to this study.

Received March 18, 2015 Revised April 23, 2015 Accepted May 26, 2015

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/ which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

This study was conducted to examine the effects of supplementing brown seaweed by-products (BSB) in the diet of ruminants on ruminal fermentation characteristics, growth performance, endocrine response, and milk production in Holstein cows. In Experiment 1, the effects of different levels (0%, 2%, and 4% of basal diet as Control, 2% BSB, 4% BSB, respectively) of BSB were evaluated at 3, 6, 9, 12, and 24 h in vitro batch culture rumen fermentation. The pH tended to be higher for the higher level of BSB supplementation, with the pH at 12 h being significantly higher (p<0.05) than that of the control. The concentration of ammonia nitrogen was lower at 3, 9, 12, and 24 h incubation (p<0.05) compared with the control, and tended to be low at other incubation times. Volatile fatty acid concentration appeared to be minimally changed while lower values were observed with 4% BSB treatment at 24 h (p<0.05). In Experiment 2, effects of levels (0%, 2%, and 4%) of BSB on growth performance, endocrine responses and milk production were studied with Holstein dairy cows during transition. Dry matter intake, daily gain and feed efficiency were not affected by BSB supplementation. The concentration of plasma estrogen for the control, 2% BSB and 4% BSB after three months of pregnancy were 55.7, 94.1, and 72.3 pg/mL, respectively (p = 0.08). Although the differences of progesterone levels between BSB treatments and the control were minimal, the concentration in 4% BSB treatment increased to 157.7% compared with the initial level of the study. Triiodothyronine and thyroxine levels were also higher after both three months and eight months of pregnancy than the initial level at the beginning of the study. In addition, BSB treatments during one month after delivery did not affect daily milk yield and composition. In conclusion, the present results indicate that supplementation of BSB did not compromise ruminal fermentation, and animal performance at lower levels and hence may have potential to be used as a safe feed ingredient in dairy cows.

Keywords: Brown Seaweed By-products; Growth Performance; Fermentation; Blood metabolites; Holstein Cows

INTRODUCTION

Brown seaweed (Undaria pinnatifida) is rich in a polysaccharide of alginic acid which has been demonstrated to suppress cholesterol absorption, and discharge heavy metals as well as act to prevent artery hardening (Kimura et al., 1996; Amano et al., 2005; Yoon et al., 2008). Acid water-soluble polysaccharide of fucoidan in the brown seaweed has shown effects of anti-coagulation of blood (Nishino et al., 2000), anti-tumor, anti-cancer activity (Haroun-Bouhedja et al., 2002; Maruyama et al., 2003) and anti-oxidation (Allen et al., 2001) and these benefits in part result from increasing thrombin, Factor Xa, urokinase-type plasminogen activator and tissue plasminogen activator. In addition, alginate oligomer, which is a degradation product of alginates by an enzyme in brown seaweed, in a large quantities can directly and indirectly influence the activation of immune system in the body by increasing cytokine secretion (Iwamoto et al., 2003) and improving the bioavailability of zinc (Yonekura and Suzuki, 2003). Brown seaweed also contains a large amount of minerals with higher contents of iodine (I) and calcium (Ca) compared with other foods (Kaufmann et al., 1998).

Brown seaweed is in the diets of humans in Asian countries including Korea, Japan and some part of China, but because only the leaves of brown seaweed is commercially available a vast amount of stems and roots remain as seaweed by-products. On the other hand, many countries with coastline often have problems with seaweed, and there is a potential to use brown seaweed and its by-products for other purposes such as animal diets or a fertilizer. Studies to use seaweeds as a feed were attempted earlier (Kaufmann et al., 1998; Fleurence, 1999; Bach et al., 2008; Holdt and Kraan, 2011). However, studies with dairy cows are limited to only the effects of supplementing brown seaweed by-products (BSB) on in vitro fermentation characteristics, milk production and milk composition with little information being available for its effects on growth, reproduction and milk production after parturition in dairy cows. In the present study therefore, the effects of BSB on fermentation characteristics in the rumen have been examined in vitro, and then the influence of adding BSB in the diet of Holstein dairy cattle on animal performance, endocrine responses, and milk production were investigated.

MATERIALS AND METHODS

The present study consisted of two experiments. In Experiment 1, the effect of different levels of BSB on fermentation characteristics in vitro was examined, while in Experiment 2 the influence of supplementing BSB on growth, endocrine responses, and milk production of Holstein cow was studied.

Experiment 1: Effect of different levels of BSB on fermentation characteristics in the rumen in vitro

Experimental design and diets

The study involved an examination of fermentation characteristics in the rumen using in vitro batch culture in triplicate with supplementation of BSB at various levels, namely 0% (control), 2% (2% BSB), and 4% (4% BSB) of dry matter, having replaced hay in the basal diets. Basal diets consisted of a mixture with commercial concentrates and hay approximately in the ratio of 35:65 as incubation substrates (Tables 1 and 2).

Preparation of rumen inoculum and incubation procedure

Rumen inoculum used was obtained from a Holstein cow equipped with a permanent ruminal cannula. Once being taken, rumen contents were transferred to a laboratory using a thermos bottle kept at 39°C, immediately after which the rumen content was filtered with four layers cheesecloth to remove feed particles, and stored in a constant temperature bath maintained at 39°C. The filtered rumen fluid was mixed with McDougal’s buffer (McDougall, 1948) bubbled with CO₂ in 1:1 ratio, and used as a rumen inoculum. First, 0.25 g of substrate was placed in a 120 mL serum bottle, into which 25 mL of rumen inoculum was added under anaerobic conditions. The bottles were plugged with a butyl-rubber stopper and aluminum cap, and were incubated in a shaking incubator (SI-600R, Lab. Companion, Seoul, Korea) maintained at 39°C, 120 rpm, where the incubation times were 0, 3, 6, 9, 12, and 24 h. After completion of each incubation time, the pH was measured immediately using a pH meter (inoLab pH Level 1, Weilheim, Germany), and supernatant was sampled after centrifugation at 3,000 rpm for 15 min, and stored at −20°C for the analyses of ammonia nitrogen (NH₃-N) and volatile fatty acids (VFA). For VFA analysis, 4 mL of supernatant was added to 1 mL of 25% HPO₃ and stored at −72°C.

Sample analysis

Dry matter (DM), crude protein, ether extracts, organic matter, Ca and phosphorus of basal diets and BSB used were analyzed according to the method of AOAC (1995), and acid detergent fiber and neutral detergent fiber were analyzed according to the method of Van Soest et al. (1991). Analysis of ammonia-N was determined by using a spectrophotometer (Optizen 1142H, MECASYS Co., Ltd, Daejeon, Korea) after color fixation in the same quantities for phenol and alkali according to Chaney and Marbach (1962). An analysis of VFA was made with gas chromatography (VARIAN CP-3800, Varian Inc., Walnut Creek, CA, USA) according to the method by Erwin et al (1961) with a fused silica capillary column (30 m×0.32 mm, 0.5 μm film thickness, HP Innowax, Agilent Technologies Inc., Santa Clara, CA, USA) equipped with flame ionization detector.

Experiment 2: Effect of supplementing BSB on growth, endocrine status, and milk production of Holstein dairy cows

Experimental design and animals

Initially, twenty-one Holstein heifers (average body weight 419 kg) were randomly divided into 3 groups, consisting of control, 2% (2% BSB) and 4% (4% BSB) supplementation of BSB by replacing a relatively similar portion of tall fescue based on nutritional requirements (Tables 1 and 2), and the experiment was conducted for 12 months at the research farm of Seoul National University, Korea. All experimental procedures were in accordance with the “Guidelines for Care and Use of Experimental Animals of Konkuk University”.

Feeding management

All heifers were offered feed based on their nutritional requirements with the target body weight gain at 0.7 kg/d, depending on their body weights and weight gains as shown by National Research Council (2001). Concentrates mixed with BSB were offered twice a day at 8:30 AM and 16:00 PM, and tall fescue was fed at 65% of DM intake with water and mineral blocks. Chemical composition of BSB was same as the one used in Experiment 1 (Tables 1 and 2). Body weight was measured at 9:00 AM at intervals of 2 months and at the end of the study. Animal performance in terms of daily gain and feed intake was measured for 9 months. Two months after beginning the experiment, artificial insemination of heifers was implemented by a specialized inseminator after confirmation of estrus. Most heifers gave birth to calves, and milk samples were collected (see below for the sampling procedure). However, 2 animals from the control and 1 animal from 2% BSB and 4% BSB fail to give a birth and hence were omitted from blood and milk sampling.

Sample collection and analysis

Ten-mL of blood was collected from the jugular veins in a heparin-treated vacuum tube (BD Vacutainer Systems Preanalytical Solutions, Becton, Dickinson and Company, Franklin Lakes, NJ, USA) at 9:00 AM before the start of the experiment, on 120th day and 240th day of pregnancy. After collection, the plasma was separated by centrifugation (4°C, 3,000 rpm, 15 min), and stored at −70°C until further analysis. Milk production was recorded daily by automatic recording with ALPRO SYSTEM (Alfa-Laval Agri., Peterborough, Ontario, Canada), and 30 days after parturition the milk was analyzed for milk protein, milk fat, lactose and solid-not-fat (SNF) using Milkoscan-133B (Foss, Hilleroed, Denmark), and the number of somatic cells was determined by using Fossomatic-300 (Foss).

Analysis of total estrogen, progesterone, triiodothyronine (T3) and thyroxine (T4) in blood was as follows; Total estrogen was measured by radioimmunoassay (RIA) method using DA Total Estrogen kit (ICN Biomedicals, Irvine, CA, USA), and progesterone measured using CoAT-A-OUNT Progesterone kit (Diagnostic Products Corporation, Los Angeles, CA, USA). T3 and T4 were determined by RIA method using RIA-mat-T3 and RIA-mat-T4 kits (Byk-Sangtec Diagnostica, Dietzenbach, Germany).

Calculation and statistical analysis

All the results for Experiments 1 and 2 were subjected to analysis of variance with the level of BSB as the main effect using SAS version 8.1 (SAS Institute Inc., Cary, NC, USA) (SAS Institute Inc., 2000). Mean values for each treatment were further tested by Duncan’s multiple range test, and the significance was declared when p<0.05.

RESULTS AND DISCUSSION

Experiment 1: Effect of different levels of BSB on fermentation characteristics in the rumen in vitro

The pH in vitro changed very little, ranging from 6.20 to 6.63 when BSB was supplemented at different levels (Table 3). The pH above 6.00 at 24 h of incubation in all treatments indicates replacing tall fescue with BSB does not cause any unfavorable fermentative environment for microorganisms. In the case of ammonia-N concentrations, supplementation of BSB at 4% showed a lower (p<0.05) ammonia-N at 3, 9, 12, and 24 h of incubation as compared with the control.

Ammonia-N values above 5 mg/dL in the rumen are known to be optimal for microbial growth (Satter and Slyter, 1974), although there are large discrepancies among studies (i.e., 1.4 mg/Dl [Schaefer et al., 1980] to 19.4 mg/dL [Mehrez et al., 1977]). The large quantities polysaccharides present in brown seaweed exist in structural carbohydrates including alginic acid, fucoidan and laminaran, and consists of heteropolysaccharides such as D-mannuronic acid and its isomer of L-guluronic acid, which account for most of the cell walls of Phaeophyceae, including brown seaweed (Beresford et al., 2000; Klinkenberg et al., 2001). These polysaccharides can be easily degraded by the rumen microbes and act as an energy for the microbes in the rumen (Greenwood et al., 1983; Beresford et al., 1999). Hence, reduction in ammonia-N with supplemented BSB is likely to occur due to synchronization between energy and N for the growth of rumen microorganisms. Concentrations of VFA were not different except for 24 h of incubation where total VFA concentration was lower (p<0.05) when 4% BSB was supplemented (Table 4). It is unclear why VFA concentration with 4% BSB diet at 24 h was lower than that in the other dietary treatments. One might speculate that DMD (dry matter degradability) is lower with 4% BSB; however, it is difficult to conclude this as we did not obtain results on DMD.

From the results of the in vitro study, the BSB supplementation did not change ruminal pH with little variation at high level of concentrate in the diets, and may show potential to improve N metabolism in the rumen without a particular influence on the generation of VFA for other than 24 h of fermentation. Thus it was not considered that supplementation of BSB in the diets of ruminants had an unfavorable influence on the fermentation characteristics in the rumen.

Experiment 2: Influence of adding BSB on growth, endocrine response, and milk production of Holstein dairy cows during transition

Animal performance

Animal performance in terms of daily gain and feed intake of Holstein cows is presented in Table 5. Daily gains with an average weight of 419 kg for a total of 275 days were approximately 0.7 kg/d for all three treatments as expected, indicating that addition of BSB did not influence daily gains. Alginic acids composing cell walls of seaweeds have been reported to have characteristics of forming viscous gel so that palatability preference is lowered, accompanied by a reduction in feed intakes (Beresford et al., 2000). Franklin et al. (1999) also reported that DM intake was significantly reduced as a result of daily supplementation of seaweeds for milking cows. On the other hand, the levels of supplement in the present study are not considered to have major impact on DM intake, as similar results were observed between treatments where total DM intakes were 10.58, 10.36, and 10.49 kg for the control, 2% BSB and 4% BSB, respectively. However, as this experiment was conducted with a group feeding regime and the results were presented with a mean value of all animals within a treatment, statistical analysis of the feed intake was not provided.

Endocrine responses

Influences of adding BSB on various hormones in blood are given in Table 6. The pattern of estrogen before and after pregnancy indicated a normal pattern of estrogen. In terms of both estrogen and progesterone, no particular differences per stage were indicated among treatments. T3 and T4 are hormones synthesized in the thyroid glands, where I is an important precursor for the synthesis. Pattanaik et al. (2001) reported that contents of T3 and T4 in plasma had increased significantly compared with the control when I at the level of 0.05 mg and 0.075 mg per head a day was added in the basic feeds for goats. However, a pattern of increase in hormone synthesis in the thyroid glands was not exhibited per stage in the present study. In the case of T3, only a slight increase of 3.83% and 5.87% was observed when compared with the beginning of the study for a pregnancy of 120 days and 240 days, respectively.

Milk production and composition

Milk productions and milk composition 1 month after delivery of dairy cows are given in Table 7. DM intakes showed similar results among treatments with 21.05 kg, 20.88 kg, 20.52 kg for the control, 2% BSB, 4% BSB, respectively. Although the concentrations of estrogen and progesterone during pregnancy period, which tended to show higher values for 2% BSB compared with other treatments, were expected to influence duct development causing differences in milk production, no differences in milk production were brought about with resultant values of 27.14 kg, 28.77 kg, 27.65 kg corresponding to the control, 2% BSB and 4% BSB, respectively at 4th week of lactation. Contents of milk protein, milk fat, lactose, SNF were shown to be similar among treatments, indicating that addition of BSB during pregnancy period did not have an influence in the lactation period. Our results are somewhat different compared with previous reports. For example, Bendary et al. (2013) reported increased milk yield when dairy cows were supplemented with the mixture of seaweed and premix, and another study also has shown a similar result, an increased milk yield in high-yielding dairy cows (Hostens et al., 2011). The discrepancy in terms of milk yield between previous studies and our results remains to be determined. It is interesting to note, however, that in the report by Kellogg et al. (2006) where they concluded from a series of studies that supplementation of commercially available brown seaweed such as Tasco (Acadian Seaplants Ltd., Dartmouth, Nova Scotia, Canada) is beneficial for milk production in large dairy cows during moderate to severe heat stress, but not with cows at first-lactation where the body size is still relatively small compared with mature cows.

IMPLICATIONS

The present study examined the influence of BSB on fermentation characteristics in vitro and also on animal performance, endocrine response and milk production in Holstein dairy cows. From the results of both in vitro (Experiment 1) and in vivo studies (Experiment 2), it is concluded that addition of BSB hardly changes pH, induces fermentation synchronization in vitro and has little influence on estrogen and progesterone, and no increase in milk production was observed up to 1 month after delivery. The results from our study may provide an insight in the use of by-products or waste materials in the diet of dairy cows from fisheries.

Notes

CONFLICT OF INTEREST

We certify that there is no conflict of interest with any financial organization regarding the material discussed in the manuscript.

ACKNOWLEDGMENTS

This research was supported by Bio-industry Technology Development Program (313002031HD020) for Ministry of Agriculture, Food and Rural Affairs, Republic of Korea.

Table 1

Chemical composition of feeds used in Experiments 1 and 2 (% of dry matter unless otherwise stated)

Item	Diets

	Concentrate	Tall fescue	BSB
Crude protein	13.50	14.21	8.37
Ether extract	2.00	3.47	0.87
Crude fiber	10.00	26.16	11.53
Crude ash	15.00	6.24	35.84
Ca	0.90	0.14	1.05
P (mg/100 g)	0.50	0.02	0.24
I (mg/100 g)	-	-	7.8
Total digestible nutrients	68.00	51.00	43.20

BSB, brown seaweed by-products.

Table 2

Ingredient and chemical composition of experimental diets used in Experiments 1 and 2 (% of dry matter unless otherwise stated)

Item	Control	2% BSB	4% BSB
Ingredient
Concentrate	36.49	37.17	35.09
Tall fescue hay	63.51	60.93	61.47
BSB	0	1.90	3.44
Total	100.0	100.0	100.0
Chemical composition
Dry matter	89.57	89.50	89.52
Crude protein	13.95	13.84	13.76
Ether extract	2.89	2.83	2.82
Neutral detergent fiber	52.14	51.46	51.76
Acid detergent fiber	27.53	27.07	27.34
Ca	0.45	0.47	0.47
P	0.33	0.33	0.33
I (ppm)	-	1.35	2.70
Total digestible nutrients	57.15	57.12	56.64

BSB, brown seaweed by-products.

Table 3

Effects of dietary BSB supplementation on in vitro pH and ammonia nitrogen (NH₃-N) concentration in Experiment 1

Incubation time (h)	Treatments1			SEM	p-value

	Control	2% BSB	4% BSB
pH
3	6.62	6.60	6.63	0.009	0.546
6	6.51	6.51	6.53	0.008	0.535
9	6.39	6.37	6.39	0.007	0.460
12	6.26b	6.30a	6.30a	0.005	0.028
24	6.22	6.20	6.22	0.014	0.747
NH₃-N (mg/dL)
3	7.66a	6.44a,b	5.05b	0.368	0.072
6	4.94	4.44	4.66	0.241	0.711
9	6.74a	6.98a	3.44b	0.497	0.047
12	8.00a	6.71a,b	4.74b	0.485	0.085
24	18.10a	14.03b	10.43c	0.570	0.005

BSB, brown seaweed by-products; SEM, standard error of the mean.

¹ All values represent the mean of triplicates.

^a,b,c Means in the same row with different superscripts differ (p<0.05).

Table 4

Effects of dietary BSB supplementation on in vitro volatile fatty acids concentration in Experiment 1

Incubation time (h)	Treatments1			SEM	p-value

	Control	2% BSB	4% BSB
Acetate (mM)
3	45.47	48.30	46.02	1.434	0.8253
6	53.29	52.39	55.48	0.972	0.5745
9	62.51	56.41	52.96	1.884	0.0697
12	62.58	60.98	62.97	1.607	0.8789
24	71.47a	77.47a	62.40b	2.408	0.0057
Propionate (mM)
3	11.78	12.78	12.75	0.473	0.7730
6	14.52	14.64	16.20	0.430	0.3446
9	17.69	15.21	15.58	0.536	0.0738
12	17.95	17.64	19.47	0.646	0.4907
24	20.70a,b	23.69a	19.15b	0.797	0.0357
Butyrate (mM)
3	5.99	6.59	6.14	0.326	0.8504
6	7.57	7.16	7.90	0.210	0.5047
9	9.60	8.09	7.26	0.483	0.1133
12	9.65	9.09	9.25	0.407	0.8683
24	11.45a	12.06a	8.97b	0.551	0.0116
Valerate (mM)
3	0.69	0.74	0.64	0.046	0.7955
6	0.83	0.76	0.81	0.022	0.4254
9	1.05	0.90	0.72	0.065	0.0827
12	1.06	1.00	0.97	0.050	0.7851
24	1.43a	1.40a	1.08b	0.072	0.0043
Total volatile fatty acids (mM)
3	65.26	69.94	66.99	2.324	0.8332
6	77.70	76.39	82.01	1.645	0.5073
9	92.82	82.26	77.87	3.033	0.0753
12	93.33	90.64	94.55	2.740	0.8526
24	108.41a	118.14a	93.97b	3.941	0.0089

BSB, brown seaweed by-products; SEM, standard error of the mean.

¹ All values represent the mean of triplicates.

^a, b Means in the same row with different superscripts differ (p<0.05).

Table 5

Effects of dietary BSB supplementation on growth performance for 9 months in Holstein heifers in Experiment 2

Item	Control	2% BSB	4% BSB	SEM	p-value
Initial body weight (kg)	419.1	419.0	419.1	8.85	0.9997
Final body weight (kg)	612.7	610.3	611.7	17.46	0.9927
Weight gain (kg)	193.6	191.3	192.6	6.35	0.9928
Daily weight gain (kg/d)	0.70	0.70	0.70	0.023	0.9963
Feed intake (kg/d)	10.58	10.36	10.49	-	-
Tall fescue	6.78	6.38	6.45	-	-
BSB	0	0.18	0.36	-	-
Concentrate	3.80	3.78	3.58	-	-
Growth efficiency (%)	6.62	6.76	6.68	-	-

BSB, brown seaweed by-products; SEM, standard error of the mean.

Table 6

Effects of dietary BSB supplementation on endocrine response of Holstein dairy heifers in Experiment 21

Item	Control	2% BSB	4% BSB	SEM	p-value
Before BSB offered
Estrogen (pg/mL)	20.57	20.57	23.14	1.417	0.3101
Progesterone (ng/mL)	3.26	3.26	1.94	0.438	0.0917
T3 (ng/dL)	167.24	167.24	147.47	2.865	0.0163
T4 (μg/dL)	6.52	6.53	6.19	0.145	0.1531
Conception at 120 d
Estrogen (pg/mL)	55.71	94.14	72.73	7.314	0.0764
Progesterone (ng/mL)	4.92	5.84	4.61	0.450	0.4479
T3 (ng/dL)	159.69	167.71	153.12	3.695	0.1843
T4 (μg/dL)	5.95	6.25	5.35	0.235	0.1957
Conception at 240 d
Estrogen (pg/mL)	121.57	189.57	165.22	20.159	0.3871
Progesterone (ng/mL)	5.53	5.19	5.00	0.446	0.8902
T3 (ng/dL)2	160.38	167.29	156.14	2.419	0.0888
T4 (μg/dL)3	5.45	5.95	5.36	0.212	0.4149

BSB, brown seaweed by-products; SEM, standard error of the mean.

¹ Experimental animals were heifers and were conceived during the study.

² Triiodothyronine.

³ Thyroxine.

Table 7

Effects of dietary BSB supplementation on DMI, milk yield and composition of Holstein dairy cows in Experiment 2

Item	Treatments			SEM	p-value

	Control	2% BSB	4% BSB
Number of cows	5	6	6
DMI (kg/d)	21.05	20.88	20.52	0.525	0.8752
Milk yield (kg/d)	27.14	28.77	27.65	0.342	0.7963
Milk fat (%)	4.07	4.12	4.03	0.230	0.5364
Milk protein (%)	3.11	3.06	3.12	0.158	0.8897
Milk lactose (%)	4.71	4.81	4.73	0.112	0.7856
Solid-not-fat (%)	8.27	8.31	8.32	0.175	0.9982

DMI, dry matter intake; BSB, brown seaweed by-products; SEM, standard error of the mean.

REFERENCES

Allen VG, Pond KR, Saker KE, Fontenot JP, Bagley CP, Ivy RL, Evans RR, Brown CP, Miller MF, Montgomery JL, Dettle TM, Wester DB. 2001. Tasco-Farage: III. Influence of a seaweed extract on performance, monocyte immune cell response, and carcass characteristics in feedlot-finished steers. J Anim Sci 79:1032–1040.

Amano H, Kakinuma M, Coury DA, Ohno H, Hara T. 2005. Effect of seaweed mixture on serum lipid level and platelet aggregation in rats. Fish Sci 71:1160–1166.

AOAC. 1995. Official Methods of Analysis. 16th ednAssociation of Official Analytical Chemists, AOAC Inc; Washington, DC, USA:

Bach SJ, Wang Y, McAllister TA. 2008. Effect of feeding sun-dried seaweed (Ascophyllum nodosum) on fecal shedding of Escherichia coli O157 : H7 by feedlot cattle and on growth performance of lambs. Anim Feed Sci Technol 142:17–32.

Bendary MM, Bassiouni MI, Ali MF, Gaafar HM, Shamas ASh. 2013. Effect of premix and seaweed additives on productive performance of lactating friesian cows. Int Res J Agric Sci Soil Sci 3:174–181.

Beresford NA, Mayes RW, Colgrove PM, Barnett CL, Bryce L, Dodd BA, Lamb CS. 2000. A comparative assessment of the potential use of alginates and dietary calcium manipulation as countermeasures to reduce the transfer of radiostrontium to the milk of dairy animals. J Environ Radioact 51:321–334.

Beresford NA, Mayes RW, MacEachern PJ, Dodd BA, Lamb CS. 1999. The effectiveness of alginates to reduce the transfer of radiostrontium to the milk of dairy goats. J Environ Radioact 44:43–54.

Chaney AL, Marbach EP. 1962. Modified reagents for determination of urea and ammonia. Clin Chem 8:130–132.

Erwin ES, Marco GJ, Emery EM. 1961. Volatile fatty acid analyses of blood and rumen fluid by gas chromatography. J Dairy Sci 44:1768–1771.

Fleurence J. 1999. Seaweed proteins: biochemical, nutritional aspects and potential uses. Trends Food Sci Technol 10:25–28.

Franklin ST, Martin KR, Baer RJ, Schingoethe DJ, Hippen AR. 1999. Dietary marine algae (Schizochytrium sp.) increases concentrations of conjugated linoleic, docosahexaenoic and transvaccenic acids in milk of dairy cows. J Nutr 129:2048–2054.

Greenwood Y, Orpin CG, Paterson IW. 1983. Digestibility of seaweeds in Orkney sheep. In : Proceedings of the Physiological Society, Cambridge Meeting: Babraham Poster Communications; 16–18 June 1983; J Physiol. 343:p. 120

Haroun-Bouhedja F, Lindenmeyer F, Lu H, Soria C, Jozefonvicz J, Boisson-Vidal C. 2002. In vitro effects of fucans on MDA-MB231 tumor cell adhesion and invasion. Anticancer Res 22:2285–2292.

Holdt SL, Kraan S. 2011. Bioactive compounds in seaweed: functional food applications and legislation. J Appl Phycol 23:543–597.

Hostens M, Fievez V, Vlaeminck B, Buyse J, Leroy J, Piepers S, De Vliegher S, Opsomer G. 2011. The effect of marine algae in the ration of high-yielding dairy cows during transition on metabolic parameters in serum and follicular fluid around parturition. J Dairy Sci 94:4603–4615.

Iwamoto Y, Xu X, Tamura T, Oda T, Muramatsu T. 2003. Enzymatically depolymerized alginate oligomers that cause cytotoxic cytokine production in human mononuclear cells. Biosci Biotechnol Biochem 67:258–263.

Kaufmann S, Wolfram G, Delange F, Rambeck WA. 1998. Iodine supplementation of laying hen feed: a supplementary measure to eliminate iodine deficiency in humans? Z Ernährungswiss 37:288–293.

Kellogg DW, Anschutz K, Pennington J. 2006. Report of research trial with Tasco at Rose Ark Dairy in Arkansas during summer 2005. AAES Research Series 545: Arkansas Animal Science Department Report 2006Fayetteville, AR, USA: p. 100–104.

Kimura Y, Watanabe K, Okuda H. 1996. Effects of soluble sodium alginate on cholesterol excretion and glucose tolerance in rats. J Ethnopharmacol 54:47–54.

Klinkenberg G, Lystad KQ, Levine DW, Dyrset N. 2001. Cell release from alginate immobilized Lactococcus lactis ssp. lactis in chitosan and alginate coated beads. J Dairy Sci 84:1118–1127.

Maruyama H, Tamauchi H, Hashimoto M, Nakano T. 2003. Antitumor activity and immune response of Mekabu fucoidan extracted from Sporophyll of Undaria pinnatifida. In Vivo 17:245–249.

McDougall EI. 1948. Studies on ruminant saliva: 1. The composition and output of sheep’s saliva. Biochem J 43:99–109.

Mehrez AZ, Ørskov ER, McDonald I. 1977. Rates of rumen fermentation in relation to ammonia concentration. Br J Nutr 38:437–443.

National Research Council. 2001. Nutrient requirements of dairy cattle. 7th revised ednNational Academy Press; Washington, DC, USA:

Nishino T, Yamauchi T, Horie M, Nagumo T, Suzuki H. 2000. Effects of a fucoidan on the activation of plasminogen by u-PA and t-PA. Thromb Res 99:623–634.

Pattanaik AK, Khan SA, Varshney VP, Bedi SP. 2001. Effect of iodine level in mustard (Brassica juncea) cake-based concentrate supplement on nutrient utilisation and serum thyroid hormones of goats. Small Rumin Res 41:51–59.

SAS Institute Inc. 2000. User’s Guide: Statistics, release 8.1 version. SAS Institute Inc; Cary, NC, USA:

Satter LD, Slyter LL. 1974. Effect of ammonia concentration on rumen microbial protein production in vitro. Br J Nutr 32:199–208.

Schaefer DM, Davis CL, Bryant MP. 1980. Ammonia saturation constants for predominant species of rumen bacteria. J Dairy Sci 63:1248–1263.

Van Soest PJ, Robertson JB, Lewis BA. 1991. Methods for dietary fiber, neutral detergent fiber, and nonstartch polysaccharides in relation to animal nutrition. J Dairy Sci 74:3583–3597.

Yonekura L, Suzuki H. 2003. Some polysaccharides improve zinc bioavailability in rats fed a phytic acid-containing diet. Nutr Res 23:343–355.

Yoon NY, Kim HR, Chung HY, Choi JS. 2008. Anti-hyperlipidemic effect of an edible brown algae, Ecklonia stolonifera, and its constituents on poloxamer 407-induced hyperlipidemic and cholesterol-fed rats. Arch Pharm Res 31:1564–1571.