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Article

Feeding Black Pepper (Piper nigrum) or Exogenous Xylanase Improves the Blood Lipid Profile of Broiler Chickens Fed Wheat-Based Diets

by
Vasil Radoslavov Pirgozliev
1,*,
Stephen Charles Mansbridge
1,
Isobel Margaret Whiting
1,
Kristina Kljak
2,
Artur Jozwik
3,
Judith Maria Rollinger
4,
Atanas Georgiev Atanasov
3,5 and
Stephen Paul Rose
1
1
National Institute of Poultry Husbandry, Harper Adams University, Newport TF10 8NB, UK
2
Department of Animal Nutrition, Faculty of Agriculture, University of Zagreb, 10000 Zagreb, Croatia
3
Institute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Jastrzebiec, 05-552 Magdalenka, Poland
4
Department of Pharmaceutical Sciences, Division of Pharmacognosy, University of Vienna, A-1090 Vienna, Austria
5
Ludwig Boltzmann Institute for Digital Health and Patient Safety, Medical University of Vienna, A-1090 Vienna, Austria
*
Author to whom correspondence should be addressed.
Vet. Sci. 2023, 10(9), 587; https://doi.org/10.3390/vetsci10090587
Submission received: 19 August 2023 / Revised: 13 September 2023 / Accepted: 19 September 2023 / Published: 21 September 2023
(This article belongs to the Special Issue Assessment of Oxidant and Antioxidant Status in Livestock)

Abstract

:

Simple Summary

Epidemiological research indicates that low blood plasma levels of high-density lipoprotein (HDL) and increased levels of low-density lipoprotein (LDL) are associated with an increased risk of cardiovascular diseases in humans. Yet, the impact of blood lipids on the health and wellbeing of poultry is not fully understood. This research provides information that feeding black peppercorn (BP) increases HDL and feeding xylanase (XYL) reduces LDL in the blood plasma of broiler chickens. For XYL-fed birds, this coincided with increased hepatic antioxidant capacity. Although the life span of commercial poultry is much shorter than that of humans, further understanding of the need to manipulate blood lipids for the improvement of the health and wellbeing of poultry is important. This study offers a nutritional approach to influence the production performance and health of poultry.

Abstract

This study aimed to determine the impact of dietary black peppercorn (BP) and xylanase (XYL) alone or in combination on growth performance, dietary energy, nutrient digestibility and blood lipid profile when fed to male Ross 308 broiler chickens from the ages of 7 to 21 d. A wheat-soy-based basal feed that was formulated to be 0.42 MJ lower in metabolizable energy (ME) was mixed. The basal feed was then split into four batches, with the first batch set aside as the basal control; the second batch was supplemented with freshly milled BP; the third batch was supplemented with XYL; the fourth batch was supplemented with both BP and XYL, as in the previous two batches. Each diet was fed to eight pens, with two birds in a pen, following randomization. Feeding BP reduced bird growth and most of the digestibility coefficients but increased blood high-density lipoprotein (p < 0.05). Dietary XYL increased bird growth, dietary ME and nutrient digestibility (p < 0.05). In addition, XYL increased hepatic carotenoids and coenzyme Q10, but reduced blood low-density lipoprotein (p < 0.05). There were no BP by XYL interactions (p > 0.05) observed. Further research is needed to identify the optimum level of BP in broiler diets.

1. Introduction

The inclusion of dietary plant extracts to poultry diets is gaining popularity, not only for being used as an alternative to antimicrobial growth promotors [1] but also for their antioxidant properties [2] and potential health benefits [3]. Animal studies showed that the long-term intake of synthetic antioxidants, e.g., butylated hydroxyanisole and butylated hydroxytoluene [4,5], may lead to health risks including skin allergies, gastrointestinal tract (GIT) disorders and the increased likelihood of cancer [6,7]. Natural antioxidants, such as vitamin E and carotenoids, play important roles in maintaining poultry health and the productive and reproductive performance of breeders, layers, rearing birds and growing broilers [8]. Thus, studying the impact of antioxidants from natural origin, e.g., plant extracts from natural spices, on the health and welfare of poultry is an important aspect of nutritional research.
Black pepper (Piper nigrum L.) is a tropical plant belonging to the Piperaceae family and cultivated for its peppercorns (BP). It is native to parts of the Malabar Coast of India and is one of the earliest known spices. Black pepper is also well known for its use as a food ingredient and in traditional Chinese and Indian medicine [9]. The principal bioactive component of BP fruits, piperine, is an alkaloid that has a wide range of pharmacological effects, including antioxidant, anti-bacterial, anti-proliferative and anti-tumour and cholesterol-lowering properties [10]. Studies with rats have indicated that dietary BP can elevate the blood plasma levels of high-density lipoprotein (HDL) and decrease the plasma levels of total cholesterol (TC), triglyceride (TG) and low-density lipoprotein (LDL) cholesterol [11]. However, others [12] did not find changes in blood lipid variables attributed to feeding BP to broiler chickens. Previous research [9] showed that feeding BP to growing pigs increased HDL and vitamin C in blood. It has been reported [13] that feeding BP to poultry decreases blood TC. Dietary BP does not consistently affect the growth of broiler chickens, since [14,15] did not find enhanced growth performance, whilst dietary BP reduced the growth performance in other studies [16] or was found to be dose-dependent [13,17].
Exogenous xylanase (XYL) has been routinely used in poultry diets for over three decades. The mode of XYL action is mainly associated with a reduction in digesta viscosity, improved digestion and absorption of nutrients, dietary energy availability and the generation of fibres with prebiotic properties, leading to the improved growth performance of broilers [18,19]. Beyond performance results, it has been reported [20] that dietary XYL increases blood HDL and reduces TC, although it was not identified previously [21]. Recently, it has been reported that dietary XYL increases hepatic vitamin E [22] and coenzyme Q10 [23] when fed to broiler chickens, suggesting antioxidant properties. In addition, there is lack of information on the interaction between dietary BP and supplementary XYL.
Blood mineral composition can be affected by diet, bird strain, sex, age and season [24], although information on birds fed BP and XYL is limited. No difference was found in blood sodium and potassium concentrations of birds fed BP [12]. An increase in blood phosphorus in broilers fed a mixture of phytase and XYL was found, but no differences in calcium level was found [25]. Whilst this limited information is available, there is a general lack of knowledge on the interaction between BP and XYL when fed to broiler chickens. Since XYL is known to modulate nutrient digestibility and absorption, including minerals, in combination with the bioactive properties of BP, an interaction may be expected. Thus, the experiment aimed to investigate the effect of dietary BP and XYL, alone or in combination, on growth performance, relative GIT organ weight, the availability of dietary energy and nutrients, hepatic antioxidant concentration, blood lipids and mineral profiles of broiler chickens. To avoid confounding with antioxidants in maize, a wheat-based diet was chosen [20,21].

2. Materials and Methods

2.1. Experimental Diets and BP Sample

A wheat-soy-based basal grower feed that was approximately 0.42 MJ (100 kcal) lower than the breeder’s recommendations (Aviagen Ltd., Edinburgh, UK) was mixed for the experiment (Table 1). Black peppercorns (registered feed material: ID number 009237-EN) with a determined amount of 42 g/kg piperine were purchased from the market (Sainsburys, UK) (Table 2).
The basal feed was then split into four batches, with the first batch set aside as the basal control portion; the second batch was supplemented with an Aspergillus oryzae commercial preparation of endo-1,4-beta-XYL at 200 FXU/kg (Ronozyme WX (CT), DSM, Kaiseraugst, Switzerland); the third batch was supplemented with a 10 g/kg diet of freshly milled BP corns; the fourth batch was supplemented with both XYL and BP, as in the previous two batches. All diets contained 20 g/kg of acid-insoluble ash (AIA), a feed-grade diatomaceous earth (Multi-Mite®, Wiltshire, UK), as an insoluble marker. Feed was not reformulated to account for XYL or BP inclusion.

2.2. Birds, Management and Sample Collection

Eighty male Ross 308 chicks were purchased at a day old from a commercial hatchery (Cyril Bason Ltd., Craven Arms, UK). On arrival, all chicks were allocated to a single-floor pen, reared on wood shavings and fed a proprietary broiler feed. On day 7, sixty-four birds were allocated to 32 pens, two birds per pen, following randomization. Each pen (experimental unit) was equipped with a trough feeder and drinker. The room temperature was 32 °C when the chicks were a day old and was gradually reduced to 20 °C by the end of the study (21 d old). A standard lighting programme for broilers was used (Aviagen Ltd., Edinburgh, UK). For the last three days of the study, from the ages of 18 to 21 d, the solid floor in each pen was replaced with wire mesh, and excreta were collected each day. Pooled excreta were oven-dried at 60 °C and milled prior to chemical analysis. Data on growth performance, including feed intake (FI), weight gain (WG) and mortality-corrected feed conversion ratio (FCR), were obtained from 7 d to 21 d of age. At the end of the study, at 21 d of age, one bird per pen was head-only electrically stunned, and blood was collected during exsanguination (terminal blood collection) into lithium heparin tubes. Plasma was obtained via centrifugation of the blood and stored at −80 °C until analysis. The liver of the dead bird was weighed and immediately stored at −20 °C until analysis. The organs from the GIT of the same bird, including proventriculus and gizzard (PG), duodenum (D), pancreas (P), jejunum (J), ileum (I), caeca and the spleen, were weighed and processed as previously described [26].

2.3. Laboratory Analyses

Piperine in BP was determined at the Department of Pharmacognosy, University of Vienna (Austria) [27]. Starch and non-starch polysaccharides (NSPs) in basal feed and BP were determined by Englyst Carbohydrates Ltd. (Southampton, UK), following standard methodology [28,29]. Dry matter (DM), crude protein (CP; 6.25 × N) and oil (crude fat, CF) in feed and excreta samples were determined following standard procedures as previously described [30]. The gross energy (GE) in feed, BP and excreta samples was determined using a Parr 6200 isoperibol oxygen bomb calorimeter (Parr Instrument Co., Moline, IL, USA). Neutral detergent fibres (NDFs) in samples were determined as previously described [31]. Acid-insoluble ash (AIA) in feed and excreta was determined by following the standard procedure [32]. The antioxidants in basal feed, BP and liver, including vitamin E, coenzyme Q10 and total carotenoids (TCS), were determined as previously described [33,34]. Blood plasma analyses including total cholesterol (TC), high-density lipoprotein (HDL), low-density lipoproteins (LDL), triglyceride (TG), total protein (TP), Ca, P, Fe and Mg were also performed [9,35,36].

2.4. Statistical Analysis

Data analyses were performed in Genstat (23rd edition) statistical software (IACR Rothamstead, Hertfordshire, UK). Comparisons among the studied variables were performed via two-way ANOVA using a 2 × 2 factorial design (dietary BP × xylanase). Outliers, homogeneity and normality of residuals were assessed prior to the ANOVA. In all instances, differences were reported as significant at p < 0.05.

3. Results

The determined chemical composition of the basal diet and BP are presented in Table 2. Black pepper contained less CP, but more CF, GE, starch, carotenoids and coenzyme Q10 compared to the basal diet. The total NSP content in the BP and the basal diet was similar (Table 2).
The results of bird growth performance, AMEn and total tract nutrient digestibility coefficients are presented in Table 3.
Birds fed the BP diet had lower final BWs (p < 0.001), lower daily FIs (p < 0.05), lower WGs (p < 0.001), higher FCRs (p < 0.001) and lower DMD, ND and NDFD values (p < 0.05) compared to those fed BP-free diets. Dietary BP did not influence dietary AMEn and FD (p > 0.05). Feeding XYL improved the final BW, daily FI, daily WG, AMEn, DMD, ND and NDFD coefficients (p < 0.05). There was no diet by XYL interaction observed (Table 3).
Table 4 presents information on relative GIT organ weights. Feeding BP increased (p < 0.05) the relative weight of D and J.
Whilst dietary XYL overall did not significantly affect the weight of SI, when fed alone (without BP), it reduced the relative weight of SI (p < 0.05). Similarly, feeding dietary XYL alone reduced the relative weight of GIT compared to the combination of BP and XYL (p < 0.05); however, this was not different to the basal control or BP-only diets.
Dietary XYL increased the hepatic concentration of TCS and coenzyme Q10 (p < 0.05) (Table 5).
There was a tendency of BP by XYL interaction (p = 0.067) as feeding diet containing both, BP and XYL, numerically increased hepatic vitamin E concentration (basal feed, 74 µg/g; BP feed, 75 µg/g; XYL feed, 63 µg/g; BP and XYL feed, 88 µg/g; SEM = 6.34).
Feeding BP resulted in increased HDL (p < 0.05) and reduced Ca (p < 0.05) in blood plasma (Table 6). Feeding XYL reduced (p < 0.05) blood LDL level. No differences were found for other studied variables in blood (p > 0.05). There was no BP by XYL interaction observed.

4. Discussion

The chemical composition of BP was within the expected range [9,27,37]. It is recognized that the composition of plants, e.g., wheat [38], naturally varies due to different climate, soil, agronomy, cultivars, geographical regions, processing and laboratory analysis techniques. The popularity of foods with high antioxidant content is increasing; thus, the observed levels of coenzyme Q10 (103 µg/g) in BP may be used to enhance animal and human diets. Several different diseases have been associated with pro-oxidative processes [39,40], and the improvement of antioxidant defences of the body has been considered as a preventive and therapeutic strategy [41,42].
Chickens fed non-BP-containing diets had 12% lower body weight than breeders’ recommendations, which was expected and can be explained by them being fed mash rather than pelleted feed and kept in small groups [43,44], although this was not considered to be detrimental to the experimental aims. However, birds fed BP had an average body weight that was 31% lower compared to breeders’ recommendations, which is in addition to a 21.4% reduction in FI compared to non-BP-fed birds. Previous research also showed a sort of dose-dependent manner in the response of FI and growth to dietary BP [17]. In general, lower BP inclusion, i.e., about 5 g/kg, did not have an impact, although the inclusion of 10 g/kg or more led to reduced FI and overall growth performance [13,16]. Birds’ feed intake is affected primarily by feed’s visual and textural properties, but taste and smell can also influence it [45,46]. Piperine, the main active ingredient in BP, is a naturally occurring pungent and spicy constituent of BP and may bring more intensive dietary flavour when added in greater levels [47]. A study feeding piperine to rats [48] reported reduced FI and WG in those fed 50 mg/kg body weight. Additionally, it has been reported that the introduction of as little as 20 mg of piperine per kg in the diet inhibited the volume of gastric juice, gastric acidity, and pepsin of rats and mice [49]. In the present study, the birds fed BP were consuming 58.2 g of feed daily (14-day feeding period), containing 0.58 g of BP or about 24 mg of piperine, which is about 46 mg/kg of the average daily body weight (523 g). Thus, indicating that the dietary level of piperine in the reported study was high for rats and may therefore also be potentially high for chickens, though further research is required to confirm the tolerances of chickens to piperine. These high levels of piperine may be the reason for the observed lower digestibility and performance results.
In agreement with recent studies [19,23,50], dietary XYL increased the final BW, daily FI, daily WG, AMEn and nutrient digestibility coefficients. Exogenous XYL has been routinely used in poultry nutrition to hydrolyze NSP and improve the feeding quality of fibre-rich diets [18,51]. The beneficial effect of XYL in wheat-based diets is mainly attributed to the reduction in digesta viscosity, improving digestion and absorption of nutrients, dietary energy availability and the subsequent growth performance of chickens [52,53]. The observed differences in the enhancement of bird growth performance, available energy and digestion in the literature are attributed to variations in dietary fibre [38], birds’ age and study duration [44], the transit rate of digesta in various segments of the broilers’ GIT [54] and rearing environment [55].
Although feed materials are the main determinant of antioxidant composition in the liver [34], feed supplements/additives other than antioxidants (e.g., phytase and XYL) can affect the efficiency of antioxidant assimilation from the diet and subsequently their accumulation in the liver [3,56,57]. An increase in hepatic vitamin E and coenzyme Q10 content, respectively, when feeding XYL to broilers has been also reported [22,23]. The mode of action of XYL accounting for the observed increase in hepatic carotenoids and coenzyme Q10 in XYL fed birds is unclear. A high concentration of coenzyme Q10 in cell membranes enhances their antioxidant status against lipid peroxidation. In agreement with previous research [23], the observed increase in hepatic antioxidants suggests that dietary XYL improves not only dietary energy and nutrient availability, but also the antioxidant status within commercial poultry. The increased AMEn, DMD, ND and NDFD of the birds fed XYL diets in the present study is coupled with reduced SI weights. In general, if the efficiency of digestion is consistently suboptimal, whether due to ingredient quality, microbial interaction or anti-nutritive factors, the GIT responds by increasing in both size (surface area) and digestive enzyme output [58].
The results of blood plasma lipid fractions, TP, Ca and P were within the expected range for broiler chickens [24]. The responses in HDL and LDL in blood are supported by previous research with BP in rats [11], pigs [9] and with XYL in broilers [20]. Epidemiological research shows that low blood levels of HDL and high levels of LDL are associated with an increased risk of cardiovascular diseases in humans [59,60]. There are similarities in lipid metabolism between chickens and humans that make birds a suitable model for investigation [61]; thus, a balance between blood lipids may also be important for their health and wellbeing. Sudden death syndrome (SDS), one of the main reasons for mortality in growing broilers, is also associated with heart problems (acute heart failure) as a potential cause of the disease in broiler chickens [62]. However, the use of BP and XYL in the reported study elicited favourable responses in levels of HDL and LDL; thus, they may have the potential to decrease the incidence of SDS in broilers. It can be also speculated that the inclusion of BP and XYL to broiler diets, alone or in combination, may not only enhance the health of the birds but may also reduce the unhealthy lipid fraction in meat, bringing further benefits to consumer health. Low-density lipids and HDL are two main classes of lipoproteins synthesized and secreted by the liver. The triglycerides are primarily used for LDL and most of the phospholipids and cholesterol are in HDL [63]. It has been found that changes in LDL and HDL production may relate to fatty liver haemorrhagic syndrome in laying hens [64,65]. Thus, further research on feeding BP and other plant extracts on bird health is warranted.

5. Conclusions

The inclusion of 10 g/kg of BP to broiler diets increased blood plasma HDL but reduced production performance, including the growth rate of the birds. Dietary XYL, however, reduced blood plasma LDL and increased hepatic antioxidants concentrations, as well as improved bird growth and the availability of dietary energy and nutrients. The lack of interaction between BP and XYL shows that when fed together, these supplements do not cause detrimental effects. Further work is needed to establish the optimum level of dietary BP for poultry; however, XYL can be fed as standard.

Author Contributions

Conceptualization and experimental design, V.R.P., I.M.W. and S.P.R.; laboratory analysis, I.M.W., K.K., A.J., A.G.A. and J.M.R.; statistical analysis, V.R.P., S.C.M. and I.M.W.; writing—original draft preparation, V.R.P., S.C.M., I.M.W. and S.P.R.; writing—review and editing, V.R.P., S.C.M., I.M.W., K.K., A.J., J.M.R., A.G.A. and S.P.R. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted at the National Institute of Poultry Husbandry and approved by the Harper Adams University Research Ethics Committee, UK, Project number 0783-201910-STAFF. The manuscript has been prepared to comply with the ARRIVE 2.0 guidelines [66].

Informed Consent Statement

Not applicable.

Data Availability Statement

The data that support the findings of this study are available on reasonable request from the corresponding author.

Acknowledgments

The authors acknowledge the technical assistance of Richard James and Conor Westbrook of The National Institute of Poultry Husbandry at Harper Adams University.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Whiting, I.M.; Pirgozliev, V.; Kljak, K.; Orczewska-Dudek, S.; Mansbridge, S.C.; Rose, S.P.; Atanasov, A.G. Feeding dihydroquercetin in wheat-based diets to laying hens: Impact on egg production and quality of fresh and stored eggs. Br. Poult. Sci. 2022, 63, 735–741. [Google Scholar] [CrossRef] [PubMed]
  2. Pirgozliev, V.; Mansbridge, S.C.; Rose, S.P.; Mackenzie, A.M.; Beccaccia, A.; Karadas, F.; Ivanova, S.G.; Staykova, G.P.; Oluwatosin, O.O.; Bravo, D. Dietary essential oils improve feed efficiency and hepatic antioxidant content of broiler chickens. Animal 2019, 13, 502–508. [Google Scholar] [CrossRef] [PubMed]
  3. Karadas, F.; Pirgozliev, V.; Pappas, A.C.; Acamovic, T.; Bedford, M.R. Effects of different dietary phytase activities on the concentration of antioxidants in the liver of growing broilers. J. Anim. Physiol. Anim. Nutr. 2010, 94, 519–526. [Google Scholar] [CrossRef] [PubMed]
  4. Botterweck, A.; Verhagen, H.; Goldbohm, R.; Kleinjans, J.; Brandt, P.V.D.; Brandt, P.V.D. Intake of butylated hydroxyanisole and butylated hydroxytoluene and stomach cancer risk: Results from analyses in the Netherlands Cohort Study. Food Chem. Toxicol. 2000, 38, 599–605. [Google Scholar] [CrossRef] [PubMed]
  5. Saad, B.; Sing, Y.Y.; Nawi, M.A.; Hashim, N.; Mohamedali, A.; Saleh, M.I.; Sulaiman, S.F.; Talib, K.; Ahmad, K.; Ali, A.S.M. Determination of synthetic phenolic antioxidants in food items using reversed-phase HPLC. Food Chem. 2007, 105, 389–394. [Google Scholar] [CrossRef]
  6. Randhawa, S.; Bahna, S.L. Hypersensitivity reactions to food additives. Curr. Opin. Allergy Clin. Immunol. 2009, 9, 278–283. [Google Scholar] [CrossRef] [PubMed]
  7. Lourenço, S.C.; Moldão-Martins, M.; Alves, V.D. Antioxidants of natural plant origins: From sources to food industry applications. Molecules 2019, 24, 4132. [Google Scholar] [CrossRef] [PubMed]
  8. Surai, P.F.; Kochish, I.I. Nutritional modulation of the antioxidant capacities in poultry: The case of selenium. Poult. Sci. 2019, 98, 4231–4239. [Google Scholar] [CrossRef]
  9. Yang, Y.; Kanev, D.; Nedeva, R.; Jozwik, A.; Rollinger, J.M.; Grzybek, W.; Pyzel, B.; Yeung, A.W.K.; Uhrin, P.; Breuss, J.M.; et al. Black pepper dietary supplementation increases high-density lipoprotein (HDL) levels in pigs. Curr. Res. Biotechnol. 2019, 1, 28–33. [Google Scholar] [CrossRef]
  10. Siddiqui, S.; Khushtar, M.; Zafar, A.; Hasan, S.M.; Arshad, M.; Ahmad, M.A.; Kashif, M.; Mujahid, M. Mechanism-based physiological effects of piperine: A Review. Curr. Pharmacol. Rep. 2023, 9, 117–127. [Google Scholar] [CrossRef]
  11. Meriga, B.; Parim, B.; Chunduri, V.R.; Naik, R.R.; Nemani, H.; Suresh, P.; Ganapathy, S.; Vvu, S.B. Antiobesity potential of Piperonal: Promising modulation of body composition, lipid profiles and obesogenic marker expression in HFD-induced obese rats. Nutr. Metab. 2017, 14, 72. [Google Scholar] [CrossRef] [PubMed]
  12. Akbarian, A.; Golian, A.; Kermanshahi, H.; Gilani, A.; Moradi, S. Influence of turmeric rhizome and black pepper on blood constituents and performance of broiler chickens. Afr. J. Biotechnol. 2012, 11, 8606–8611. [Google Scholar]
  13. Singh, J.; Sharma, M.; Mehta, N.; Singh, N.D.; Kaur, P.; Sethi, A.P.S.; Sikka, S.S. Influence of supplementation of black pepper powder through feed in broiler chickens on their growth performance, blood profile, meat sensory qualities and duodenum morphology. Indian J. Anim. Sci. 2018, 88, 215–221. [Google Scholar] [CrossRef]
  14. Hosseini, M.N. Comparison of using different level of black pepper with probiotic on performance and serum composition on broilers chickens. J. Basic Appl. Sci. Res. 2011, 1, 2425–2428. [Google Scholar]
  15. Olayemi, W.A.; Williams, G.A.; Olatidoye, O.P.; Omofunmilola, E.O. Influence of dietary inclusion of phytobiotics on growth performance, carcass and organ weight of broiler chickens. J. Agric. Food. Sci. 2020, 18, 26–38. [Google Scholar] [CrossRef]
  16. Ndelekwute, E.K.; Afolabi, K.D.; Uzegbu, H.O.; Unah, U.L.; Amaefule, K.U. Effect of dietary Black pepper (Piper nigrum) on the performance of broiler. Bangladesh J. Anim. Sci. 2015, 44, 120–127. [Google Scholar] [CrossRef]
  17. Puvača, N.; Kostadinović, L.; Ljubojević, D.; Lukač, D.; Lević, J.; Popović, S.; Novakov, N.; Vidović, B.; Đuragić, O. Effect of garlic, black pepper and hot red pepper on productive performances and blood lipid profile of broiler chickens. Eur. Poult. Sci. 2015, 79, 1–13. [Google Scholar]
  18. Bedford, M.R. The evolution and application of enzymes in the animal feed industry: The role of data interpretation. Br. Poult. Sci. 2018, 59, 486–493. [Google Scholar] [CrossRef]
  19. Šimić, A.; González-Ortiz, G.; Mansbridge, S.C.; Rose, S.P.; Bedford, M.R.; Yovchev, D.; Pirgozliev, V.R. Broiler chicken response to xylanase and fermentable xylo-oligosaccharide supplementation. Poult. Sci. 2023, 102, 103000. [Google Scholar] [CrossRef]
  20. Saleh, A.A.; Kirrella, A.A.; Abdo, S.E.; Mousa, M.M.; Badwi, N.A.; Ebeid, T.A.; Nada, A.L.; Mohamed, M.A. Effects of dietary xylanase and arabinofuranosidase combination on the growth performance, lipid peroxidation, blood constituents, and immune response of broilers fed low-energy diets. Animals 2019, 9, 467. [Google Scholar] [CrossRef]
  21. Ahmad, Z.; Butt, M.S.; Hussain, R.; Ahmed, A.; Riaz, M. Effect of oral application of xylanase on some hematological and serum biochemical parameters in broilers. Pak. Vet. J. 2013, 33, 388–390. [Google Scholar]
  22. Pirgozliev, V.; Karadas, F.; Rose, S.P.; Fernándes Beccaccia, A.; Mirza, M.W.; Amerah, A.M. Dietary xylanase increases hepatic vitamin E concentration of chickens fed wheat based diet. J. Anim. Feed Sci. 2015, 24, 80–84. [Google Scholar] [CrossRef]
  23. Pirgozliev, V.; Mansbridge, S.; Whiting, I.; Abdulla, J.; Rose, S.; Kljak, K.; Johnson, A.; Drijfhout, F.; Atanasov, A. The benefits of exogenous xylanase in wheat–soy based broiler chicken diets, consisting of different soluble non-starch polysaccharides content. Poultry 2023, 2, 123–133. [Google Scholar] [CrossRef]
  24. Meluzzi, A.; Primiceri, G.; Giordani, R.; Fabris, G. Determination of blood constituents reference values in broilers. Poult. Sci. 1992, 71, 337–345. [Google Scholar] [CrossRef] [PubMed]
  25. Sobhi, B.M.; Morsi, A.S.; Ahmed, Z.S.O.; Gamal, A.M.; Fahmy, K.N.E.D. The potential enhancing effect of both phytase and β-xylanase enzymes on performance, bone mineralization and nutrient absorption in broiler chicken. J. Adv. Vet. Res. 2023, 13, 806–814. [Google Scholar]
  26. Abdulla, J.M.; Rose, S.P.; Mackenzie, A.M.; Ivanova, S.G.; Staykova, G.P.; Pirgozliev, V.R. Nutritional value of raw and micronised field beans (Vicia faba L. var. minor) with and without enzyme supplementation containing tannase for growing chickens. Arch. Anim. Nutr. 2016, 70, 350–363. [Google Scholar] [CrossRef] [PubMed]
  27. Chauhan, R.A.J.A.N.I.; Dwivedi, J.A.Y.A.; Siddiqui, A.A. Chemical Standardization and quantification of Piperin from methanolic extract of Piper nigrum by HPLC method on the basis of isolated markers. Int. J. Chem. Sci. 2008, 6, 1726–1733. [Google Scholar]
  28. Englyst, H.N.; Quigley, M.E.; Hudson, G.J. Determination of dietary fibre as nonstarch polysaccharides with gas-liquid chromatographic, high-performance liquid chromatographic or spectrophotometric measurement of constituent sugars. Analyst 1994, 119, 1497–1509. [Google Scholar] [CrossRef]
  29. Englyst, K.N.; Hudson, G.J.; Englyst, H.N. Starch Analysis in Food. In Encyclopaedia of Analytical Chemistry; Meyers, R.A., Ed.; John Wiley and Sons: Chichester, UK, 2000; pp. 4246–4262. [Google Scholar]
  30. Whiting, I.; Pirgozliev, V.; Rose, S.P.; Karadas, F.; Mirza, M.W.; Sharpe, A. The temperature of storage of a batch of wheat distillers dried grains with solubles samples on their nutritive value for broilers. Br. Poult. Sci. 2018, 59, 76–80. [Google Scholar] [CrossRef]
  31. Van Soest, P.V.; Robertson, J.B.; Lewis, B.A. Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. J. Dairy Sci. 1991, 74, 3583–3597. [Google Scholar] [CrossRef]
  32. Van Keulen, J.Y.B.A.; Young, B.A. Evaluation of acid-insoluble ash as a natural marker in ruminant digestibility studies. J. Anim. Sci. 1977, 44, 282–287. [Google Scholar] [CrossRef]
  33. Karadas, F.; Pirgozliev, V.; Rose, S.P.; Dimitrov, D.; Oduguwa, O.; Bravo, D. Dietary essential oils improve the hepatic antioxidative status of broiler chickens. Br. Poult. Sci. 2014, 55, 329–334. [Google Scholar] [CrossRef]
  34. Gunjević, V.; Zurak, D.; Grbeša, D.; Kiš, G.; Međimurec, T.; Pirgozliev, V.; Kljak, K. Bioaccessibility of tocols in commercial maize hybrids determined by an in vitro digestion model for poultry. Molecules 2023, 28, 5015. [Google Scholar] [CrossRef] [PubMed]
  35. Jóźwik, A.; Strzałkowska, N.; Bagnicka, E.; Grzybek, W.; Krzyżewski, J.; Poławska, E.; Kołataj, A.; Horbańczuk, J.O. Relationship between milk yield, stage of lactation, and some blood serum metabolic parameters of dairy cows. Czech J. Anim. Sci. 2012, 57, 353–360. [Google Scholar] [CrossRef]
  36. Oso, A.O.; Williams, G.A.; Oluwatosin, O.O.; Bamgbose, A.M.; Adebayo, A.O.; Olowofeso, O.; Pirgozliev, V.; Adegbenjo, A.A.; Osho, S.O.; Alabi, J.O.; et al. Effect of dietary supplementation with arginine on haematological indices, serum chemistry, carcass yield, gut microflora, and lymphoid organs of growing turkeys. Livest. Sci. 2017, 198, 58–64. [Google Scholar] [CrossRef]
  37. Milenković, A.N.; Stanojević, L.P. Black pepper: Chemical composition and biological activities. Adv. Technol. 2021, 10, 40–50. [Google Scholar] [CrossRef]
  38. Azhar, M.R.; Rose, S.P.; Mackenzie, A.M.; Mansbridge, S.C.; Bedford, M.R.; Lovegrove, A.; Pirgozliev, V.R. Wheat sample affects growth performance and the apparent metabolisable energy value for broiler chickens. Br. Poult. Sci. 2019, 60, 457–466. [Google Scholar] [CrossRef] [PubMed]
  39. Hertog, M.G.L.; Feskens, E.J.M.; Holiman, P.C.H.; Katan, M.B.; Kromhout, D. Dietary antioxidant flavonoids and risk of coronary heart disease: The Zutphen elderly study. Lancet 1993, 342, 1007. [Google Scholar] [CrossRef]
  40. Wilson, L.M.; Tharmarajah, S.; Jia, Y.; Semba, R.D.; Schaumberg, D.A.; Robinson, K.A. The effect of lutein/zeaxanthin intake on human macular pigment optical density: A systematic review and meta-analysis. Adv. Nutr. 2021, 12, 2244–2254. [Google Scholar] [CrossRef]
  41. Pirgozliev, V.; Mansbridge, S.C.; Rose, S.P.; Lillehoj, H.S.; Bravo, D. Immune modulation, growth performance, and nutrient retention in broiler chickens fed a blend of phytogenic feed additives. Poult. Sci. 2019, 98, 3443–3449. [Google Scholar] [CrossRef]
  42. Yeung, A.W.K.; Choudhary, N.; Tewari, D.; El Demerdash, A.; Horbanczuk, O.K.; Das, N.; Pirgozliev, V.; Lucarini, M.; Durazzo, A.; Souto, E.B.; et al. Quercetin: Total-scale literature landscape analysis of a valuable nutraceutical with numerous potential applications in the promotion of human and animal health—A review. Anim. Sci. Pap. Rep. 2021, 39, 199–212. [Google Scholar]
  43. Pirgozliev, V.; Mirza, M.W.; Rose, S.P. Does the effect of pelleting depend on the wheat sample when fed to chickens? Animal 2016, 10, 571–577. [Google Scholar] [CrossRef] [PubMed]
  44. Yang, Z.; Pirgozliev, V.R.; Rose, S.P.; Woods, S.; Yang, H.M.; Wang, Z.Y.; Bedford, M.R. Effect of age on the relationship between metabolizable energy and digestible energy for broiler chickens. Poult. Sci. 2020, 99, 320–330. [Google Scholar] [CrossRef] [PubMed]
  45. Gillette, K.; Thomas, D.K.; Bellingham, W.P. A parametric study of flavoured food avoidance in chicks. Chem. Senses 1983, 8, 41–57. [Google Scholar] [CrossRef]
  46. Ferket, P.R.; Gernat, A.G. Factors that affect feed intake of meat birds: A review. Int. J. Poult. Sci. 2006, 5, 905–911. [Google Scholar]
  47. Ziegenhagen, R.; Heimberg, K.; Lampen, A.; Hirsch-Ernst, K.I. Safety aspects of the use of isolated Piperine ingested as a bolus. Foods 2021, 10, 2121. [Google Scholar] [CrossRef]
  48. Bastaki, M.; Aubanel, M.; Bauter, M.; Cachet, T.; Demyttenaere, J.; Diop, M.M.; Harman, C.L.; Hayashi, S.M.; Krammer, G.; Li, X.; et al. Absence of adverse effects following administration of piperine in the diet of Sprague-Dawley rats for 90 days. Food Chem. Toxicol. 2018, 120, 213–221. [Google Scholar] [CrossRef]
  49. Bai, Y.F.; Xu, H. Protective action of piperine against experimental gastric ulcer. Acta Pharmacol. Sin. 2000, 21, 357–359. [Google Scholar] [PubMed]
  50. Whiting, I.M.; Pirgozliev, V.; Bedford, M.R. The effect of different wheat varieties and exogenous xylanase on bird performance and utilization of energy and nutrients. Poult. Sci. 2023, 102, 102817. [Google Scholar] [CrossRef]
  51. Whiting, I.M.; Pirgozliev, V.; Rose, S.P.; Wilson, J.; Amerah, A.M.; Ivanova, S.G.; Staykova, G.P.; Oluwatosin, O.O.; Oso, A.O. Nutrient availability of different batches of wheat distillers dried grains with solubles with and without exogenous enzymes for broiler chickens. Poult. Sci. 2017, 96, 574–580. [Google Scholar] [CrossRef]
  52. Bedford, M.R.; Classen, H.L. Reduction of intestinal viscosity through manipulation of dietary rye and pentosanase concen-tration is effected through changes in the carbohydrate-composition of the intestinal aqueous phase and results in improved growth-rate and food conversion efficiency of broiler chicks. J. Nutr. 1992, 122, 560–569. [Google Scholar] [PubMed]
  53. Whiting, I.M.; Rose, S.P.; Mackenzie, A.M.; Amerah, A.M.; Pirgozliev, V.R. Effect of wheat distillers dried grains with solubles and exogenous xylanase on laying hen performance and egg quality. Poult. Sci. 2019, 98, 3756–3762. [Google Scholar] [CrossRef] [PubMed]
  54. Duve, L.R.; Steenfeldt, S.; Thodberg, K.; Nielsen, B.L. Splitting the scotoperiod: Effects on feeding behaviour, intestinal fill and digestive transit time in broiler chickens. Br. Poult. Sci. 2011, 52, 1–10. [Google Scholar] [CrossRef] [PubMed]
  55. Pirgozliev, V.; Bravo, D.; Rose, S.P. Rearing conditions influence nutrient availability of plant extracts supplemented diets when fed to broiler chickens. J. Anim. Physiol. Anim. Nutr. 2014, 98, 667–671. [Google Scholar] [CrossRef] [PubMed]
  56. Karadas, F.; Pirgozliev, V.; Acamovic, T.; Bedford, M.R. The effects of dietary phytase activity on the concentration of Co-enzyme Q10 in the liver of young turkeys and broilers. Br. Poult. Abs. 2005, 1, 1–74. [Google Scholar] [CrossRef]
  57. Pirgozliev, V.; Karadas, F.; Pappas, A.; Acamovic, T.; Bedford, M.R. The effect on performance, energy metabolism and hepatic carotenoid content when phytase supplemented diets were fed to broiler chickens. Res. Vet. Sci. 2010, 89, 203–205. [Google Scholar] [CrossRef] [PubMed]
  58. Bedford, M.R. Effect of non-starch polysaccharidases on avian gastrointestinal function. In Avian Gut Function in Health and Disease; Perry, G.C., Ed.; Carfax Publishing Company: Oxfordshire, UK, 2006; pp. 159–170. [Google Scholar]
  59. Kardassis, D.; Mosialou, I.; Kanaki, M.; Tiniakou, I.; Thymiakou, E. Metabolism of HDL and its regulation. Curr. Med. Chem. 2014, 21, 2864–2880. [Google Scholar] [CrossRef]
  60. Rye, K.A.; Barter, P.J. Regulation of high-density lipoprotein metabolism. Circ. Res. 2014, 114, 143–156. [Google Scholar] [CrossRef]
  61. Piekarski, A.; Greene, E.; Anthony, N.B.; Bottje, W.; Dridi, S. Crosstalk between autophagy and obesity: Potential use of avian model. Adv. Food Technol. Nutr. Sci. Open J. 2015, 1, 32–37. [Google Scholar] [CrossRef]
  62. Sosnówka-Czajka, E.; Skomorucha, I. Sudden death syndrome in broiler chickens: A review on the etiology and prevention of the syndrome. Ann. Anim. Sci. 2022, 22, 865–871. [Google Scholar] [CrossRef]
  63. Hermier, D. Lipoprotein metabolism and fattening in poultry. J. Nutr. 1997, 127, 805S–808S. [Google Scholar] [CrossRef]
  64. Dong, X.; Tong, J. Different susceptibility to fatty liver-haemorrhagic syndrome in young and older layers and the interaction on blood LDL-C levels between oestradiols and high energy-low protein diets. Br. Poult. Sci. 2019, 60, 265–271. [Google Scholar] [CrossRef]
  65. Lin, C.W.; Huang, T.W.; Peng, Y.J.; Lin, Y.Y.; Mersmann, H.J.; Ding, S.T. A novel chicken model of fatty liver disease induced by high cholesterol and low choline diets. Poult. Sci. 2021, 100, 100869. [Google Scholar] [CrossRef]
  66. Percie du Sert, N.; Hurst, V.; Ahluwalia, A.; Alam, S.; Avey, M.T.; Baker, M.; Browne, W.J.; Clark, A.; Cuthill, I.C.; Dirnagl, U.; et al. The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research. PLoS Biol. 2020, 18, e3000411. [Google Scholar]
Table 1. Composition of broiler chicken basal feed (g/kg, as-fed) used in the experiment.
Table 1. Composition of broiler chicken basal feed (g/kg, as-fed) used in the experiment.
Ingredients (g/kg)Basal Feed
Wheat651.0
Soybean meal (48% CP)219.7
Soybean meal (full fat)50.0
Vegetable oil20.0
Dicalcium phosphate14.5
Limestone12.5
NaCl1.7
Lysine2.7
Methionine3.9
Vitamin/mineral premix 14.0
Acid-insoluble ash20.0
100
Calculated analysis (as fed):
Crude protein g/kg206
ME MJ/kg 12.67
Crude fat g/kg44.4
Ca g/kg9.7
Available P g/kg4.6
Lysine g/kg12.4
Methionine + cysteine g/kg9.9
1 The vitamin and mineral premix contained vitamins and trace elements to meet the breeder’s recommendation (Aviagen Ltd., Edinburgh, UK). The premix provided is as follows (units/kg diet): retinol 3600 μg, cholecalciferol 125 μg, α-tocopherol 34 mg, menadione 3 mg, thiamine 2 mg, riboflavin 7 mg, pyridoxine 5 mg, cobalamin 15 μg, nicotinic acid 50 mg, pantothenic acid 15 mg, folic acid 1 mg, biotin 200 μg, iron 80 mg, copper 10 mg, manganese 100 mg, cobalt 0.5 mg, zinc 80 mg, iodine 1 mg, selenium 0.2 mg and molybdenum 0.5 mg.
Table 2. Determined chemical composition of basal feed and black pepper (as-fed basis).
Table 2. Determined chemical composition of basal feed and black pepper (as-fed basis).
Determined ValuesBasal FeedBlack Pepper
Dry matter (g/kg)902921
Crude protein (g/kg)218130
Crude fat (g/kg)3555
Gross energy (MJ/kg)15.5117.15
Piperine (g/kg)Nd42
Starch (g/kg)429491
Soluble non-starch polysaccharides (NSPs, g/kg)369
Insoluble non-starch polysaccharides (NSPins, g/kg)6083
Total non-starch polysaccharides (NSPt, g/kg)9692
Neutral detergent fibres (NDF, g/kg)84Nd
Total carotenoids (µg/g)0.0662.777
Vitamin E (µg/g)21.2Nd
Coenzyme Q10 (µg/g)2103
MJ = megajoule; Nd = not determined.
Table 3. Effect of dietary black pepper (BP) and xylanase (XYL) on start and end body weight (BW), daily feed intake (FI), weight gain (WG), mortality-corrected feed conversion ratio (FCR), N-corrected apparent metabolizable energy (AMEn), total tract dry matter (DMD), nitrogen (ND), fat (FD) and neutral detergent fibre (NDFD) digestibility coefficients when fed to broiler chickens from 7 to 21 d of age 1.
Table 3. Effect of dietary black pepper (BP) and xylanase (XYL) on start and end body weight (BW), daily feed intake (FI), weight gain (WG), mortality-corrected feed conversion ratio (FCR), N-corrected apparent metabolizable energy (AMEn), total tract dry matter (DMD), nitrogen (ND), fat (FD) and neutral detergent fibre (NDFD) digestibility coefficients when fed to broiler chickens from 7 to 21 d of age 1.
TreatmentBW 7 d
(g)
BW 21 d
(g)
FI
(g/b/d)
WG
(g/b/d)
FCR
(g:g)
AMEn
(MJ/kg DM)
DMDNDFDNDFD
BP
  No17589765.751.61.27612.950.7340.6520.6530.247
  Yes17970258.237.41.56712.760.7160.6120.6660.190
XYL
  No17576759.342.21.43812.710.7190.6160.6450.190
  Yes17883364.646.81.40413.000.7320.6470.6740.247
SEM1.816.61.461.170.02590.0920.00450.00740.02330.0177
Probabilities
BP0.115<0.0010.006<0.001<0.0010.1670.0120.0080.7010.033
XYL0.2980.0100.0190.0120.3650.0390.0480.0410.3870.036
BP × XYL0.4490.3960.6670.4380.4900.3110.1920.7920.3940.889
1 Each mean represents values from sixteen replicate pens for main effects; AMEn and digestibility coefficients were determined between 18 and 21 d of age; SEM = pooled standard errors of mean.
Table 4. Effect of dietary black pepper (BP) and xylanase (XYL) on the relative organ weight expressed as the percent of bird body weight (BW) of gastrointestinal tract (GIT), including proventriculus and gizzard (PG), duodenum (D), jejunum (J), ileum (I), small intestine (SI), caeca, pancreas, liver and spleen of 21 d old broiler chickens 1.
Table 4. Effect of dietary black pepper (BP) and xylanase (XYL) on the relative organ weight expressed as the percent of bird body weight (BW) of gastrointestinal tract (GIT), including proventriculus and gizzard (PG), duodenum (D), jejunum (J), ileum (I), small intestine (SI), caeca, pancreas, liver and spleen of 21 d old broiler chickens 1.
TreatmentBW
(g)
PGDJISICaecaPancreasGITLiver
BP
  No9112.971.642.612.146.390.750.4410.543.57
  Yes6922.781.862.862.176.890.720.4310.813.82
XYL
  No7802.841.692.792.216.690.720.4410.683.73
  Yes8232.911.812.682.116.590.750.4310.683.66
SEM-0.1100.0510.0660.0690.1330.0270.0210.1650.149
BP  XYL
No  No8823.031.612.752.31 a6.67 a0.720.4710.88 ab3.74
No  Yes9402.911.682.471.97 b6.11 b0.770.4110.20 a3.39
Yes  No6792.641.782.832.10 ab6.71 a0.710.4110.47 ab3.71
Yes  Yes7062.911.932.902.24 ab7.07 a0.720.4511.15 b3.92
-0.1550.0720.0660.0980.1890.0390.0300.2340.210
Probabilities
BP-0.3570.0080.0140.7410.0160.4310.6900.2690.246
XYL-0.8380.1380.2670.3110.6110.4020.7500.9970.738
BP × XYL-0.3410.5960.0710.0230.0240.6170.1490.0090.204
1 Each mean represents values from sixteen replicate pens for main effects; GIT = gastrointestinal tract weight without liver; SEM = pooled standard errors of mean; means with different superscripts are statistically significant (p < 0.05). a,b Statistically significant (p < 0.05) difference.
Table 5. Effect of dietary black pepper (BP) and xylanase (XYL) on hepatic carotenoids, vitamin E and coenzyme Q10 of 21 d old broiler chickens 1.
Table 5. Effect of dietary black pepper (BP) and xylanase (XYL) on hepatic carotenoids, vitamin E and coenzyme Q10 of 21 d old broiler chickens 1.
TreatmentCarotenoids
(µg/g)
Vitamin E
(µg/g)
Coenzyme Q10
(µg/g)
BP
  No1.4469418
  Yes1.4981402
XYL
  No1.3375375
  Yes1.6076444
SEM0.0734.520.8
Probabilities
BP0.6680.0600.603
XYL0.0150.8360.030
BP × XYL0.5250.0670.646
1 Each mean represents values from sixteen replicate pens for main effects; SEM = pooled standard errors of mean.
Table 6. Effect of dietary black pepper (BP) and xylanase (XYL) on blood plasma variables of 21 d old broiler chickens 1.
Table 6. Effect of dietary black pepper (BP) and xylanase (XYL) on blood plasma variables of 21 d old broiler chickens 1.
TreatmentTC
(mmol/L)
HDL
(mmol/L)
LDL
(mmol/L)
TRIGL
(mmol/L)
TP
(g/L)
Ca
(mmol/L)
P
(mmol/L)
BP
No4.12.90.551.3922.63.32.10
Yes4.43.10.611.3724.03.01.88
XYL
No4.33.00.661.3723.33.22.14
Yes4.13.00.511.3923.33.11.84
SEM0.1330.070.0370.1410.670.070.1145
Probabilities
BP0.1770.0170.2780.9160.1740.0220.176
XYL0.4010.9180.0100.9160.9530.9470.073
BP × XYL0.5000.8570.1030.5660.3430.9790.429
1 Each mean represents values from sixteen replicate pens for main effects; TC = total cholesterol; HDL = high-density lipoproteins; LDL = low-density lipoproteins; TG = triglyceride; TP = total protein; Ca = calcium; P = phosphorus; SEM = pooled standard errors of mean.
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Pirgozliev, V.R.; Mansbridge, S.C.; Whiting, I.M.; Kljak, K.; Jozwik, A.; Rollinger, J.M.; Atanasov, A.G.; Rose, S.P. Feeding Black Pepper (Piper nigrum) or Exogenous Xylanase Improves the Blood Lipid Profile of Broiler Chickens Fed Wheat-Based Diets. Vet. Sci. 2023, 10, 587. https://doi.org/10.3390/vetsci10090587

AMA Style

Pirgozliev VR, Mansbridge SC, Whiting IM, Kljak K, Jozwik A, Rollinger JM, Atanasov AG, Rose SP. Feeding Black Pepper (Piper nigrum) or Exogenous Xylanase Improves the Blood Lipid Profile of Broiler Chickens Fed Wheat-Based Diets. Veterinary Sciences. 2023; 10(9):587. https://doi.org/10.3390/vetsci10090587

Chicago/Turabian Style

Pirgozliev, Vasil Radoslavov, Stephen Charles Mansbridge, Isobel Margaret Whiting, Kristina Kljak, Artur Jozwik, Judith Maria Rollinger, Atanas Georgiev Atanasov, and Stephen Paul Rose. 2023. "Feeding Black Pepper (Piper nigrum) or Exogenous Xylanase Improves the Blood Lipid Profile of Broiler Chickens Fed Wheat-Based Diets" Veterinary Sciences 10, no. 9: 587. https://doi.org/10.3390/vetsci10090587

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