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Effects of Bile Acids and Lipase Supplementation in Low-Energy Diets on Growth Performance, Fat Digestibility and Meat Quality in Broiler Chickens

ABSTRACT

The aim of this study was to investigate the effect of bile acids and lipase supplementation in low energy (LE) diets on growth, fat digestibility, serum lipid profile and meat quality of broilers. Seven hundred one-day-old broiler chicks were divided into 5 dietary treatments with five replicates of 28 birds each. The five treatments were: i) high energy diet (HE; metabolizable energy (ME) = 3,000 and 3,170 kcal/kg for starter and finisher diet), ii) low energy diet (LE; ME = 2,900 and 3,070 kcal/kg for starter and finisher diet), iii) LE diet supplemented with 300 g/ton bile acids (LEB), iv) LE diet supplemented with 180 g/ton lipase (LEL), v) LE diet supplemented both with bile acids (300 g/ton) and lipase (180 g/ton). The experiment lasted 35 days having starter phase from days 1-21 and finisher phase from days 22-35. Dietary inclusion of both bile acids and lipase in LE diet had no effect (p>0.05) on body weight (BW) gain and feed intake. High energy diet reduced feed intake and BW gain during starter and overall period; however, during finisher phase BW gain was similar in all dietary treatments. Dietary energy level had no effect on feed conversion ratio. Fat digestibility (p>0.05) both in the starter and finisher phase was not affected by the dietary treatments. Concentration of total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol and triglycerides were not affected by the dietary treatments (p>0.05). Meat quality of breast and thigh muscle was unaffected due to the dietary treatments (p>0.05). It is concluded that the supplementation of bile acids alone or in combination with lipase in low-energy diets did not improve broiler performance, fat digestibility, serum lipid profile and meat quality.

Keywords:
Digestibility; enzyme; energy density; fat; meat quality

INTRODUCTION

Animal fats and vegetable oils are being used in broiler diets to increase energy density and improve growth performance (Leeson and Summers, 2005Leeson S, Summers J. Commercial poultry production. Guelph: University Books ;2005. p.63-64.; Abudabos, 2014Abudabos A. Effect of fat source, energy level and enzyme supplementation and their interactions on broiler performance. South African Journal of Animal Science 2014;44(3):80-87.; Wu, 2018WU G. Principles of animal nutrition. Boca Raton: CRC Press; 2018.). However, fat addition negatively affects fat digestibility (Tancharoenrat et al., 2013Tancharoenrat P, Ravindran V, Zaefarian F, Ravindran G. Influence of age on the apparent metabolisable energy and total tract apparent fat digestibility of different fat sources for broiler chickens. Animal Feed Science and Technology 2013;86(3-4):186-192.; Siyal et al., 2017Siyal FA, Babazadeh D, Wang C, Arain MA, Saeed M, Ayasan T, et al. Emulsifiers in the poultry industry. World’s Poultry Science Journal 2017;73(3):611-620.) especially during early broiler age (Tancharoenrat et al., 2013; Ravindran et al., 2016Ravindran V, Tancharoenrat P, Zaefarian F, Ravindran G. Fats in poultry nutrition: Digestive physiology and factors influencing their utilisation. Animal Feed Science and Technology 2016;213:1-21.). Immature physiological function of the pancreas in broilers results in less production of bile acids and pancreatic lipase during early ages (Wiseman & Lewis, 1998Wiseman J, Lewis CE. Influence of dietary energy and nutrient concentration on the growth of body weight and of carcass components of broiler chickens. The Journal of Agricultural Science 1998;131(3):361-371.; Al-Marzooqi & Leeson, 1999Al-Marzooqi W, Leeson S. Evaluation of dietary supplements of lipase, detergent, and crude porcine pancreas on fat utilization by young broiler chicks. Poultry Science 1999;78(11):1561-1566.; Lilburn & Loeffler, 2015Lilburn MS, Loeffler S. Early intestinal growth and development in poultry. Poultry Science 2015;94(7):1569-1576.; Classen, 2017Classen HL. Diet energy and feed intake in chickens. Animal Feed Science and Technology 2017;233:13-21.), which may leads to poor fat digestibility.

Recently, bile acids are getting attention as dietary emulsifier for increasing fat digestibility (Upadhaya et al., 2019bUpadhaya SD, Yun KS, Zhao PY, Lee IS, Kim IH. Emulsifier as a feed additive in poultry and pigs-a review. Animal Nutrition and Feed Technology 2019b;19(2):323-336.) and improving broiler performance (Maisonnier et al., 2003Maisonnier S, Gomez J, Bree A, Berri C, Baeza E, Carre B. Effects of microflora status, dietary bile salts and guar gum on lipid digestibility, intestinal bile salts, and histomorphology in broiler chickens. Poultry Science 2003;82(5):805-814.; Parsaie et al., 2007Parsaie S, Shariatmadari F, Zamiri MJ, Khajeh K. Influence of wheat-based diets supplemented with xylanase, bile acid and antibiotics on performance, digestive tract measurements and gut morphology of broilers compared with a maize-based diet. British Poultry Science 2007;48(5):594-600.). Supplementation of bile acids in broiler diet significantly improve the digestibility of fat (Nazir, 2014; Hemati Matin et al., 2016; Lammasak et al., 2019Lammasak K, Kijpakorn S, Angkanaporn K. Corrigendum to: Porcine bile powder supplementation of a high fat broiler diet in relation to growth performance and nutrient digestion. Animal Production Science 2019;59(7):1310-1317.). Similarly, other studies (Ge et al., 2018Ge XK, Wang AA, Ying ZX, Zhang LG, Su WP, Cheng K, et al. Effects of diets with different energy and bile acids levels on growth performance and lipid metabolism in broilers. Poultry Science 2018;98(2):887-895.; Lai et al., 2018aLai W, Cao A, Li J, Zhang W, Zhang L. Effect of high dose of bile acids supplementation in broiler feed on growth performance, clinical blood metabolites, and organ development. The Journal of Applied Poultry Research 2018a;27(4):532-539.; Lai et al., 2018b) reported that the supplementation of bile acids improve daily weight gain, feed conversion ratio (FCR) and carcass yield in broilers.

Like bile acids, exogenous lipase also improves physiological limitation of poultry digestive system (Nagargoje et al., 2016Nagargoje S, Dhumal MV, Nikam MG, Khose KK. Effect of crude soy lecithin with or without lipase on performance and carcass traits, meat keeping quality and economics of broiler chicken. International Journal of Livestock Research 2016;6(6):46-54.). On the other hand, Hu et al. (2018Hu YD, Lan D, Zhu Y, Pang HZ, Mu XP, Hu XF. Effect of diets with different energy and lipase levels on performance, digestibility and carcass trait in broilers. Asian-Australasian Journal of Animal Sciences 2018;31(8):1275-1286.) reported that providing reduced energy diet had decreased (p<0.05) body weight (BW) gain compared to basal energy diet during a period of 14 days, however, it was compensated with the supplementation of 0.015% and 0.03% lipase. According to Wang et al. (2017), the supplementation of lipase in broiler diets improved FCR, growth performance and fat digestibility. On the contrary, other researchers reported that lipase supplementation had no effect on nutrient utilization and bird’s performance in broiler fed wheat-based diets (Polin et al., 1980Polin D, Wing TL, Ki P, Pell KE. The effect of bile acids and lipase on absorption of tallow in young chicks. Poultry Science 1980;59(12):2738-2743.; Meng et al., 2004Meng X, Slominski BA, Guenter W. The effect of fat type, carbohydrase, and lipase addition on growth performance and nutrient utilization of young broilers fed wheat-based diets. Poultry Science 2004;83(10):1718-1727.). Based on contrary results of lipase supplementation in broiler diets on performance, this study was planned to investigate the effect of supplementing bile acids and lipase in combination or alone in broiler diets on growth performance, fat digestibility, serum lipid profiles and meat quality of broiler. Our hypothesis was that feeding low energy diets supplementation with bile acids and lipase will improve broiler performance.

MATERIALS AND METHODS

All procedures carried out in this experiment were reviewed and approved by the Animal Protocol Review Committee of the University of Agriculture, Faisalabad. The experiment was conducted at the Research and Development Farm of Sharif Feed Mills (Pvt.) Limited, Okara, Pakistan.

Experimental birds, diet and housing

Seven hundred one-day-old 500 mix sex broiler chicks with an average initial BW of 45.9 ± 0.25 g were used in the trial. The chicks were randomly assigned to 5 dietary treatments with 5 replicates of 28 birds each. The five treatments were: i) high energy diet (HE; metabolizable energy (ME) = 3,000 and 3,170 kcal/kg for starter and finisher diet), ii) low energy diet (LE; ME = 2,900 and 3,070 kcal/kg for starter and finisher diet), iii) LE diet supplemented with 300 g/ton bile acids (LEB), iv) LE diet supplemented with 180 g/ton lipase (LEL), v) LE diet supplemented both with bile acids (300 g/ton) and lipase (180 g/ton). The bile acids were composed of hyocholic acid, hyodeoxycholic acid and chenodeoxycholic acid. The experiment lasted for 35 days having starter phase from days 1-21 and finisher phase from days 22-35. The composition of the experimental diets is given in Table 1. All nutrients in the experimental diets were formulated according to the nutrient requirement suggested by NRC (1994), except for ME, which was 100 kcal/kg less than recommendations for LE diets. All diets were formulated on digestible amino acids (AA) basis keeping lysine as reference AA as described in a recent study (Abdullah et al. 2019Abdullah HM, Bielke LR, Helmy YA. Effect of arginine supplementation on growth performance and immunity of broilers: A Review. Journal of Global Innovation in Agricultural and Social Sciences 2019;7(4):141-144.). Feed was offered in pellet form.

Table 1
Ingredients and nutrient analysis of experimental diets for broiler chicks (as-fed basis).

Birds in each replicate were housed in pens of 5.5’× 3.8’× 2’. Each pen had a separate tube feeder and automatic nipple drinkers. Rice husk was used for bedding material. It was ensured that the birds were not in stress and pain during the trail. Instruction of recent studies were followed to conduct the experiment (Aziz ur Rahman et al., 2017Aziz ur Rahman M, Chuanqi X, Huawei S, Binghai C. Effects of hay grass level and its physical form (full length vs. chopped) on standing time, drinking time, and social behavior of calves. Journal of Veterinary Behavior: Clinical Applications and Research 2017;21(Supplement C):7-12.; Aziz ur Rahman et al., 2019).

Data recording

To measure the feed intake, growth rate and performance parameters standard procedures were adopted as presented in the recent study (Hussain et al. 2018Hu YD, Lan D, Zhu Y, Pang HZ, Mu XP, Hu XF. Effect of diets with different energy and lipase levels on performance, digestibility and carcass trait in broilers. Asian-Australasian Journal of Animal Sciences 2018;31(8):1275-1286.; Hussain et al. 2020). In brief, the birds were weighed by pen at days 1, 21 and 35 of the experiment. Weekly feed intake was calculated, body weight gain and feed intake were recorded for the overall period.

Nutrient digestibility and chemical analysis

Acid insoluble ash (AIA) was added @ 1% as internal marker in the experimental diets for determination of nutrient digestibility. Diets with AIA were offered for 4 consecutive days. Polythene sheets were placed under the floor of all pens excreta collection. Samples were placed carefully in sampling bags as described in recent studies (Iamam-ul-Haq et al. 2019Iamam-ul-Haq, Naeem MS, Amir RM, Ilyas M, Shabir F, Ahmad I, et al. Growth and yield response of spring maize (zea mays l.) Under different potassium doses and irrigation regimes. Journal of Global Innovation in Agricultural and Social Sciences 2019;7(3):135-139.; Shahzad et al. 2019Shahzad M, Ghani WH, Ayyub M, Ali Q, Ahmad HM, Faisal M, et al. Performance of some wheat cultivars against aphid and its damage on yield and photosynthesis. Journal of Global Innovation in Agricultural and Social Sciences 2019;7(3):105-109.). . Excreta were stored at −20 °C after the removal of the feathers and scales. Feed samples from the feeders of each pen were also collected. Before chemical analysis, excreta samples were dried at 57 °C for 72 h, after which they were ground to pass through a one-mm screen. Feed and excreta content of moisture and fat was determined according to the methods of the Association of Official Analytical Chemists (AOAC, 2006) as decribed in literature (Muhammad et al. 2016Muhammad AU, Xia CQ, Cao BH. Dietary forage concentration and particle size affect sorting, feeding behaviour, intake and growth of Chinese holstein male calves. Journal of Animal Physiology and Animal Nutrition 2016;100(2):217-223.; Niu et al. 2017Niu W, He Y, Xia C, Rahman MAU, Qiu Q, Shao T, et al. Effects of replacing Leymus chinensis with whole-crop wheat hay on Holstein bull apparent digestibility, plasma parameters, rumen fermentation, and microbiota. Scientific Reports 2017;7(1):1-12.; Xia et al. 2018). Fat contents were determined by Soxhlet apparatus. Determination of AIA was performed after ashing the samples and treating the ash with boiling hydrochloric acid (Viveros et al., 2002Viveros A, Brenes A, Arija I, Centeno C. Effects of microbial phytase supplementation on mineral utilization and serum enzyme activities in broiler chicks fed different levels of phosphorus. Poultry Science 2002;81(8):1172-1183.). Digestibility procedure was followed as described in recent studies (Massuquetto et al.,2019Massuquetto A, Panisson JC, Marx FO, Surek D, Krabbe EL, Maiorka A. Effect of pelleting and different feeding programs on growth performance, carcass yield, and nutrient digestibility in broiler chickens. Poultry Science 2019;98(11):5497-5503.).

Digestibility was calculated using the following equation:

% d i g e s t i b i l i t y = 1 ( % m a r ker f e e d × % n u t r i e n t f e c e s % m a r ker f e c e s × % n u t r i e n t f e e d ) × 100

Organ index

On day 35, five birds (Pre-weighed) from each pen were slaughtered. After slaughtering the birds were defeathered, and the Bursa of fabricius, heart, liver (without gallbladder), gizzard (removal of content) and breast muscle were collected for calculation of the eviscerated weight as described in literature (Sharif et al. 2018Sharif M, Shoaib M, Rahman MAU, Ahmad F, Rehman SU. Effect of distillery yeast sludge on growth performance, nutrient digestibility and slaughter parameters in Japanese quails. Scientific Reports 2018;8(1):1-6.). Organ index was expressed as a percentage of live weight.

Serum lipid profile

On day 35, ten birds were randomly selected from each treatment (2 birds per pen) for blood collection. Serum lipid profile was determined following the procedure of previous studies (Chen et al. 2019; He et al. 2018He Y, Niu W, Qiu Q, Xia C, Shao T, Wang H, et al. Effect of calcium salt of long-chain fatty acids and alfalfa supplementation on performance of Holstein bulls. Oncotarget 2018;9(3):3029.; Su et al. 2013Su H, Wang Y, Zhang Q, Wang F, Cao Z, Rahman MAU, et al. Responses of energy balance, physiology, and production for transition dairy cows fed with a low-energy prepartum diet during hot season. Tropical Animal Health and Production. 2013;45(7):1495-1503.). Blood samples were then centrifuged at 3,000×g for 15 min and serum was separated. The total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and triglycerides (TG) in the serum samples were analyzed using a kit method on Microlab 300 (Merck, Germany).

Meat quality

Breast and thigh muscles pH was tested 24 h after slaughtering, by dipping glass-electrode in meat solution as described by (Sallam et al., 2004Sallam KI, Ishioroshi M, Samejima K. Antioxidant and antimicrobial effects of garlic in chicken sausage. LWT-Food Science and Technology 2004;37(8):849-855.). Color (lightness) of the breast and thigh muscles were measured by using handheld tristimulus colorimeter (Color Test Meter II, Neuhaus Neotec, 95808, Germany) by following the procedure of Sohaib et al. (2016Sohaib M, Butt MS, Anjum FM, Khan MI, Shahid M. Augmentation of Oxidative stability, descriptive sensory attributes and quality of meat nuggets from broilers by dietary quercetin and ALPHA‐Tocopherol regimens. Journal of Food Processing and Preservation 2016;40(3):373-385.).

Water holding capacity (WHC) was determined on breast and thigh muscles using the method of Zhang et al. (1995Zhang M, Mittal GS, Barbut S. Effects of test conditions on the water holding capacity of meat by a centrifugal method. LWT-Food Science and Technology 1995;28(1):50-55.), with some modifications. Briefly, 15 ± 0.3 g of chopped lean muscle and 22.5 ml 0.6 N NaCl solution were inserted into a centrifuge tube. The centrifuge tube with the sample and solution was weighed (W1) after homogenizing, then centrifuged at 5000×g for 10 min at 4 °C. The centrifuge tube was then removed from the centrifuge machine, then the water was carefully removed from the tube and weighed again (W2). WHC was calculated according to the following formula:

% W H C = ( W 1 W 2 S a m p l e w e i g h t S a m p l e w e i g h t ) × 100

Statistical Analysis

Data were analyzed using Analysis of Variance (ANOVA) technique under completely randomized design of Minitab Statistical Software 17 (Minitab, 2010Minitab I. Minitab statistical software. Release 17. State College; 2010.) with the cage being considered as the experimental unit. Tukey’s test was used to separate difference means among treatments. Data were assumed to be statistically significant when p<0.05 and variability in the data was expressed as the standard error means.

RESULTS

Growth performance

Dietary inclusion of bile acids and lipase separately or in combination in LE diet did not differ (p>0.05) BW gain and feed intake in starter phase. Feed intake and BW gain was lower (p<0.05) in broilers fed HE diet than other dietary treatments during starter phase and in the overall period. FCR was not affected (p>0.05) by the dietary treatments during the starter phase of the experiment. However, during finisher and overall period HE treatment had better FCR (p<0.05) as compared to LE treatment (Table 2).

Table 2
Effect of dietary bile acids and lipase enzyme supplementation on growth performance in broiler chickens.

Fat Digestibility

Reducing the energy in diet did not affect (p>0.05) fat digestibility compared to HE diet. Furthermore, the addition of bile acids and lipase alone or in combination in LE diet caused no difference (p>0.05) in fat digestibility both at 21 and 35 d of age (Table 3).

Table 3
Effect of dietary bile acids and lipase enzyme supplementation on fat digestibility in broiler chickens.

Organ index

The effect of bile acids and lipase supplementation in LE diets are presented in Table 4. Dietary treatments had no effect (p>0.05) on relative weights of bursa of fabricius, gizzard, heart, liver, spleen, abdominal fat and breast muscle.

Table 4
Effect of dietary bile acids and lipase enzyme supplementation on the relative organ weights in broiler chickens.

Serum lipid profile

Concentration of TC, HDL-C, LDL-C and TG were not affected (p>0.05) by all dietary treatments (Table 5).

Table 5
­- Effect of dietary bile acids and lipase enzyme supplementation on serum lipid profile of broiler chickens at 35 d of age.

Meat quality

Dietary treatments had no effect on WHC and pH of breast and thigh muscles. Furthermore, dietary treatments caused no difference (p>0.05) in breast and thigh muscles lightness (Table 6).

Table 6
Effect of dietary bile acids and lipase enzyme supplementation on the meat quality of breast and thigh muscle in broiler chickens.

DISCUSSION

In the current study, feed intake was not affected by the supplementation of bile acids and lipase in LE diet during starter, finisher and the overall period. However, LE diet intake was more as compared to HE diet which is similar with the findings of Harrington et al. (2015Harrington D, Sims M, Kehlet AB. Effect of Bacillus subtilis supplementation in low energy diets on broiler performance. Journal of Applied Poultry Research 2015;25(1):29-39.) and Hosseini et al. (2018Hosseini SM, Nourmohammadi R, Nazarizadeh H, Latshaw JD. Effects of lysolecithin and xylanase supplementation on the growth performance, nutrient digestibility and lipogenic gene expression in broilers fed low‐energy wheat‐based diets. Journal of Animal Physiology and Animal Nutrition 2018;102(6):1564-1573.) who reported that increased dietary energy could reduce the feed intake of broilers. Similarly, Lamot et al. (2017Lamot DM, Sapkota D, Wijtten PJ, van den Anker I, Heetkamp MJ, Kemp B, van den Brand H. Diet density during the first week of life: Effects on energy and nitrogen balance characteristics of broiler chickens. Poultry Science 2017;96(7):2294-3000.) reported that increasing diet density had reduced feed intake. Broilers have the ability to control energy intake by adjusting their feed intake based on dietary energy concentration changes (Leeson et al., 1996Leeson S, Caston L, Summers JD. Broiler response to diet energy. Poultry Science 1996;75(4):529-535.). In the current study, low intake of HE diet could be explained by the fulfillment of energy demand for broiler growth. Body weight gain was not changed by the supplementation of bile acids and lipase alone or in combination in LE diet during starter, finisher and the overall period. However, BW gain was more in LE diet compared to HE diet in starter and the overall period which is contrary to the findings of the previous researcher who reported that feeding low-energy diets reduced BW gain compared to high-energy diets during 14 d period (Zhao and Kim, 2017Zhao PY, Kim IH. Effect of diets with different energy and lysophospholipids levels on performance, nutrient metabolism, and body composition in broilers. Poultry Science 2017;96(5):1341-1347.; Hu et al., 2018Hu YD, Lan D, Zhu Y, Pang HZ, Mu XP, Hu XF. Effect of diets with different energy and lipase levels on performance, digestibility and carcass trait in broilers. Asian-Australasian Journal of Animal Sciences 2018;31(8):1275-1286.) and during the period of 28 to 35 d (Ge et al., 2018Ge XK, Wang AA, Ying ZX, Zhang LG, Su WP, Cheng K, et al. Effects of diets with different energy and bile acids levels on growth performance and lipid metabolism in broilers. Poultry Science 2018;98(2):887-895.). In birds offered reduced energy diets, they probably compensated for lower energy intake per kilogram of feed. It can explain the increased feed intake and BW of LE diets compared to HE diets. However, bile acids and lipase in LE energy diets failed to cause any improvement in feed efficiency. Decreased BW gain in the present study evidences that feed form may influence partially to the results observed (Brickett et al., 2007Brickett K, Dahiya J, Classen H, Gomis S. Influence of dietary nutrient density, feed form, and lighting on growth and meat yield of broiler chickens. Poultry Science 2007;86(10):2172-2181.; Saveewonlop et al., 2019Saveewonlop N, Rattanatabtimtong S, Ruangpanit Y, Songserm O, Attamangkune S. Effects of different phase-feeding programs with different feed forms on broiler growth performance, carcass traits and intestinal morphology. International Journal of Poultry Science 2019;18:181-186.).

The digestibility of fat was similar among all dietary treatments in the current study. It has been reported by Rabie et al. (2010Rabie MH, Ismail FS, Sherif SK. Effect of dietary energy level with probiotic and enzyme addition on performance, nutrient digestibility and carcass traits of broilers. Poultry Science 2010;30:179-201.) that digestibility of fat did not change by decreasing the energy level in the diet of broiler chicks. Similar digestibility coefficient of HE diets with LE diet could be explained by the decreased feed intake in HE diet. Although low intake increases digestibility, in present study this mechanism is failed due to high fat content in HE diet (Lammasak et al., 2019Lammasak K, Kijpakorn S, Angkanaporn K. Corrigendum to: Porcine bile powder supplementation of a high fat broiler diet in relation to growth performance and nutrient digestion. Animal Production Science 2019;59(7):1310-1317.). Our findings are similar with the findings of Dairo et al. (2010Dairo FAS, Adesehinwa AOK, Oluwasola TA, Oluyemi JA. High and low dietary energy and protein levels for broiler chickens. African Journal of Agricultural Research 2010;5(15):2030-2038.) and Papadopoulos et al. (2018Papadopoulos GA, Poutahidis T, Chalvatzi S, Di Benedetto M, Hardas A, Tsiouris V, et al. Effects of lysolecithin supplementation in low-energy diets on growth performance, nutrient digestibility, viscosity and intestinal morphology of broilers. British Poultry Science 2018;59(2):232-239.) who reported that LE or HE diet did not have any effect on fat digestibility. Similarly, Hu et al. (2018Hu YD, Lan D, Zhu Y, Pang HZ, Mu XP, Hu XF. Effect of diets with different energy and lipase levels on performance, digestibility and carcass trait in broilers. Asian-Australasian Journal of Animal Sciences 2018;31(8):1275-1286.) reported that supplementing 0.015% lipase enzyme in LE diet had similar fat digestibility compared to HE diets.

The difference in the energy level in the diet did not affect relative organ weight and breast muscle yield of broilers in the current study. Similarly, supplementation of bile acid and lipase alone or in combination in LE diet also did not affect relative organ weight and breast muscle yield of broilers. Similar organ weight and breast muscle yield of broilers in LE and HE diet are in agreement with the findings of Ge et al. (2018He Y, Niu W, Qiu Q, Xia C, Shao T, Wang H, et al. Effect of calcium salt of long-chain fatty acids and alfalfa supplementation on performance of Holstein bulls. Oncotarget 2018;9(3):3029.) and Upadhaya et al. (2019aUpadhaya SD, Rudeaux F, Kim IH. Effects of inclusion of Bacillus subtilis (Gallipro) to energy-and protein-reduced diet on growth performance, nutrient digestibility, and meat quality and gas emission in broilers. Poultry Science 2019a;98(5):2169-2178.) who reported that LE diet had no effect on liver, spleen, gizzard, abdominal fat, bursa of fabricius and breast muscle weight. Additionally, similar results were also reported by Corduk et al. (2007Corduk M, Ceylan N, Ildiz F. Effects of dietary energy density and L-carnitine supplementation on growth performance, carcass traits and blood parameters of broiler chickens. South African Journal of Animal Science 2007;37(2):65-73.) and Rabie et al. (2010Rabie MH, Ismail FS, Sherif SK. Effect of dietary energy level with probiotic and enzyme addition on performance, nutrient digestibility and carcass traits of broilers. Poultry Science 2010;30:179-201.) who stated that carcass traits of broiler chicks remained unaffected by dietary energy level. However, many researchers claimed increased percentage of abdominal fat by increasing dietary energy levels (Zhao & Kim, 2017Zhao PY, Kim IH. Effect of diets with different energy and lysophospholipids levels on performance, nutrient metabolism, and body composition in broilers. Poultry Science 2017;96(5):1341-1347.; Mohammadigheisar et al., 2018Mohammadigheisar M, Kim HS, Kim IH. Effect of inclusion of lysolecithin or multi-enzyme in low energy diet of broiler chickens. Journal of Applied Animal Research 2018;46(1):1198-1201.). In the present study, the percentage of abdominal fat was similar among HE and LE diets which might be due to lower intake of HE diets. The remaining organ index weight was also unaffected due to dietary supplementation of bile acids and lipase in the present study, which is in agreement with previous researchers (Ge et al., 2018; Hu et al., 2018Hu YD, Lan D, Zhu Y, Pang HZ, Mu XP, Hu XF. Effect of diets with different energy and lipase levels on performance, digestibility and carcass trait in broilers. Asian-Australasian Journal of Animal Sciences 2018;31(8):1275-1286.; Lai et al., 2018aLai W, Cao A, Li J, Zhang W, Zhang L. Effect of high dose of bile acids supplementation in broiler feed on growth performance, clinical blood metabolites, and organ development. The Journal of Applied Poultry Research 2018a;27(4):532-539.). Generally, gut health is considered important for better performance in livestock (Qiu et al. 2019aQiu Q, Gao C, Gao Z, He Y, Cao B, Su H. Temporal dynamics in rumen bacterial community composition of finishing steers during an adaptation period of three months. Microorganisms 2019a;7(10):410.; Qiu et al. 2019b) and external feed additives are provided to improve the gut health and performance of livestock. However, in the current study, they didn’t improve the bird’s performance.

Generally key indicators of lipid metabolism balance are TC, HDL-C and LDL-C (Helkin et al., 2016Helkin A, Stein JJ, Lin S, Siddiqui S, Maier KG, Gahtan V. Dyslipidemia part 1-review of lipid metabolism and vascular cell physiology. Vascular and Endovascular Surgery 2016;50(2):107-118.). In the current study, dietary treatments did not influence serum lipid profile of broilers. It has been reported that HE diets had no effect on serum TG, TC, HDL-C and LDL-C (Ge et al., 2018He Y, Niu W, Qiu Q, Xia C, Shao T, Wang H, et al. Effect of calcium salt of long-chain fatty acids and alfalfa supplementation on performance of Holstein bulls. Oncotarget 2018;9(3):3029.). Similar results were also reported by Zhao and Kim (2017Zhao PY, Kim IH. Effect of diets with different energy and lysophospholipids levels on performance, nutrient metabolism, and body composition in broilers. Poultry Science 2017;96(5):1341-1347.) and Hosseini et al. (2018Hosseini SM, Nourmohammadi R, Nazarizadeh H, Latshaw JD. Effects of lysolecithin and xylanase supplementation on the growth performance, nutrient digestibility and lipogenic gene expression in broilers fed low‐energy wheat‐based diets. Journal of Animal Physiology and Animal Nutrition 2018;102(6):1564-1573.) who observed that TG, TC, HDL-C and LDL-C concentrations were unaffected due to dietary energy in broilers. In the present study, bile acids supplementation in LE diet did not change serum TG, TC, HDL-C and LDL-C, which is in agreement with (Alzawqari et al., 2011Alzawqari M, Moghaddam HN, Kermanshahi H, Raji AR. The effect of desiccated ox bile supplementation on performance, fat digestibility, gut morphology and blood chemistry of broiler chickens fed tallow diets. Journal of Applied Animal Research 2011;39(2):169-174.; Ge et al., 2018; Lai et al., 2018bLai W, Huang W, Dong B, Cao A, Zhang W, Li J, et al. Effects of dietary supplemental bile acids on performance, carcass characteristics, serum lipid metabolites and intestinal enzyme activities of broiler chickens. Poultry Science 2018b;97(1):196-202.). Similarly, lipase supplementation along with bile in LE diet had similar effect as bile acid supplementation alone in LE diet. Limited studies reported the influence of lipase supplementation on blood serum profile, however, Zhao & Kim (2017) noted that supplementing 0.05% emulsifier caused no effect on serum TG, TC, HDL-C and LDL-C.

In our study, HE, LE and LE supplementation with bile acid alone or in combination with lipase had similar meat quality of breast and thigh muscles. In agreement with our results, the low-energy diet had no effect on the breast and thigh muscle color (lightness), pH value and WHC in broilers fed HE diet (Upadhaya et al., 2017Upadhaya SD, Park JW, Park JH, Kim IH. Efficacy of 1, 3-diacylglycerol as a fat emulsifier in low-density diet for broilers. Poultry Science 2017;96(6):1672-1678.; Hu et al., 2018Hu YD, Lan D, Zhu Y, Pang HZ, Mu XP, Hu XF. Effect of diets with different energy and lipase levels on performance, digestibility and carcass trait in broilers. Asian-Australasian Journal of Animal Sciences 2018;31(8):1275-1286.; Upadhaya et al., 2019a). However, limited research has been done to evaluate the quality of breast and thigh muscle in broilers fed LE diet supplemented with bile and lipase, therefore further research is needed to cross check the mechanism for the effects of bile acids on the meat quality in broilers.

CONCLUSIONS

Overall, results suggest that bile acids and lipase supplementation at 300 g/ton and 150g/ton of feed in LE diets did not affect broiler growth, digestibility, serum lipid profile and meat quality.

ACKNOWLEDGEMENTS

The authors acknowledge the Sharif Feed Mills (Pvt.) Ltd. for providing the Research and Development Farm and for the financial support of this study. We thank Dr. Muhammad Mubashar (Area Sale Manager, Asia Feed) for providing the lipase enzyme.

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Publication Dates

  • Publication in this collection
    21 Sept 2020
  • Date of issue
    2020

History

  • Received
    19 Jan 2020
  • Accepted
    19 Apr 2020
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