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South African Journal of Animal Science

On-line version ISSN 2221-4062
Print version ISSN 0375-1589

S. Afr. j. anim. sci. vol.51 n.2 Pretoria  2021

http://dx.doi.org/10.4314/sajas.v51i2.5 

ARTICLES

 

Effects of different feeding methods on neuropeptide nesfatin-1 and irisin in turkeys

 

 

F. CafI; H. InciII, #; T. AyasanIII

IVocational School of Technical Sciences University of Bingol 1200, Bingol, Turkey
IIDepartment of Animal Science, Faculty of Agriculture, Bingöl University, Bingöl 12000, Turkey
IIIOsmaniye Korkut Ata University, Kadirli Academy of Applied Sciences, Osmaniye/Turkey

 

 


ABSTRACT

In this study, the effects of different methods of feeding turkeys on the neuropeptide nesfatin-1 and the hormone irisin were evaluated. A total of 90 turkeys were distributed to three treatment groups, namely T1: conventional system, T2: 50% feed and pasture, and T3: pasture. There were 30 birds in each group with three random replications. The birds were fed for 18 weeks. At the end of the study, blood was collected from 10 birds of each group. Plasma nesfatin-1 and irisin levels were measured with an enzyme-linked immunoassay. The nesfatin-1 levels of male turkeys in T1, T2, and T3 were 0.76 ± 0.1 ng/m, 0.41 ± 0.1 ng/ml, and 1.24 ± 0.2 ng/ml, respectively. Nesfatin-1 levels in the female turkeys in T1, T2 and T3 were 0.53 ± 0.07 ng/ml, 1.18 ± 0.3 ng/ml, 1.32 ± 0.1 ng/ml, respectively. The irisin levels in the male turkeys in T1, T2, and T3 were 575.93 ± 42.5 pg/ml, 188.39 ± 1.8 pg/ml, and 607.54 ± 24.1 pg/ml, respectively. Irisin levels of the female turkeys in T1, T2 and T3 were 603.20 ± 42.2 pg/ml, 241.42 ± 18.4 pg/ml, and 399.29 ± 21.5 pg/ml, respectively. Because nesfatin-1 is involved in regulating food intake, food intake by turkeys might differ, depending on the management system. Different management systems might also alter irisin secreation because it can be induced by exercise.

Keywords: endocrine, food intake, management system


 

 

Introduction

Living organisms must consume enough energy to survive. Suppression of feed intake and the energy it supplies are important factors that can affect the nutrition, reproduction, growth, and other metabolic functions of living things negatively (Cameron et al., 1993; Steiner et al., 2003). Because Turkey imports feed resources and pays in foreign exchange, efforts to find feed resources that are cheap and are not used directly in human nutrition have gained momentum (Blake, 1993). Feed expenses constitute approximate 30% of the total cost of production for turkeys (McDougal, 2020). Thus, it is necessary to know how and how much to feed turkeys.

The hypothalamus is the main centre in which bodyweight-energy balance control is regulated (Spiegelman & Flier, 2001; Juge-Aubry et al., 2003). The lateral hypothalamus controls hunger, whereas the ventromedial hypothalamus controls satiation. These two areas work in collaboration and with other regions of the brain to maintain energy balance (Richard & Baraboi, 2004). The hypothalamus controls energy balance by evaluating the stimulating or suppressive signals received from the body systems (Havel, 2004; King, 2005). The neuropeptide nesfatin-1 is secreted from the hypothalamus and by the nervous system and peripheral tissues (Unniappan & Peter, 2005; Volkoff et al., 2005), and is responsible for the regulation of appetite (Oh-I et al., 2006; Shimizu et al., 2009; Gonzalez et al., 2010; Stengel et al., 2012) and body temperature (Könczöl et al., 2012). The nucleobindin 2 gene (NUCB2) codes for a hormone that consists of 396 amino acids and has a high amino acid sequence homology in rats, mice, and human beings (Garcia-Galiano et al., 2010). Of the 396 amino acids of NUCB2, the first 82 amino acids constitute nesfatin-1, amino acids 85-163 constitute nesfatin-2, and amino acids 166-396 constitute nesfatin-3 (Oh-I et al., 2006).

Irisin is a hormone composed of 111 amino acids with secretion induced by exercise (Boström et al., 2012). Irisin is an adipomyocine that reportedly stimulates thermogenesis by transforming white adipose tissue to brown in mammals. It is synthesized and released by many tissues with its main sources being skeletal muscle and adipose tissue (Aydin, 2014; Arhire et al., 2019).

There is limited information pertaining to irisin in non-mammalian invertebrates, including birds. For the first time, Li et al. (2015) identified irisin in chickens and indicated that it had a high degree of sequence homology with the human (97%), mouse (97%), and zebra fish (80%) hormones. Li et al. (2015) demonstrated that avian irisin was abundantly expressed in muscle, heart, pituitary gland, ovary, and brain, and in small amounts in adipose tissue, kidney, lung, testis, and the small intestine.

Nesfatin-1 and irisin are potentially effective in regulating hunger, nutrient intake, energy metabolism, bodyweight, and glucose balance. Although the effects of nesfatin-1 on humans and rats have been studied in more detail, there are few studies on poultry (e.g. Cisse, 2012; Shousha et al., 2015; Banerjee & Chaturvedi, 2015) and even less is known about the effects of irisin in birds. Previously, it was shown that turkeys fed in confinement, those that were pastured, and those in hybrid systems differed in their patterns of growth (Inci et al., 2020). Therefore, these systems were evaluated for effects on circulating levels of nesfatin-1 and irisin.

 

Material and Methods

This research was carried out in the poultry unit of the Department of Zootechnics, Faculty of Agriculture, Bingöl University. Bingöl University Experimental Ethics Committee approved the project (No 2014/09-09/03).

Day-old turkey chicks (n = 90) were distributed to three treatment groups, namely T1: conventional system, T2: 50% feed and pasture, and T3: pasture. The 30 birds that were allocated to each treatment were randomly divided into three replications of 10 birds each. The concentrate feeds that was used in T1 and T2 (Table 1) was formulated to meet the approximate needs of turkeys according to NRC (1993) norms. During the first eight weeks of their lives all poults were fed a starter diet inside. Two 60-watt bulbs were used to light the experiment room. Heat was provided by the thermostatically controlled electric stoves. The room was divided into three equal compartments that were bedded to a depth of 8 cm with wood shavings and straw. Plastic feeders with wire grills were placed in the compartments, and hygienic measures were used to ensure the health of the animals. When the poults were eight weeks old, the treatments were imposed. T1 continued to be fed concentrated feed indoors. T2 had access to pasture for eight hours a day and received 50% of concentrate feed that the T1 group consumed. T3 grazed on pasture and were not given supplemental feed. The pasture comprised alfalfa, grass, sainfoin, vetch, wheat and barley. It was sampled while it was grazed with the samples being used for nutrient analysis. The forage was 87% dry matter and contained 14.85% crude protein, 2.4% crude fat, 31.5% crude fibre, and 9.6% crude ash. The calculated energy content of the forage was 1900 kcal / kg DM. The trial ended when the birds were 18 weeks old.

At slaughter, blood was aspirated into an evacuated tube containing an anticoagulant. It was then centrifuged for 10 minutes at 3000 rpm to obtain the plasma. The plasma was transferred to 2-ml Eppendorf tubes and kept frozen at -80 °C until it was analysed (Price et al., 2007; Stengel et al., 2009). Nesfatin-1 plasma levels in turkeys were measured with a commercial kit (LSBio Inc., Seattle, Washington, USA, catalogue number LSF10671), with a measurement interval of 0.78 ng/mL to 50 ng/mL. The intra- and inter-assay coefficients of variation and sensitivity for nesfatin-1 were lower than 5.3% and 7.1%, respectively. The ELISA assays of nesfatin-1 had a sensitivity of < 0.78 ng/mL. Irisin plasma levels were measured with a commercial kit (LSBio Inc., Seattle, Washington, USA; catalogue no LS-F13185), with a measurement interval of 78 pg/mL to 5000 pg/mL. The intra- and inter-assay coefficients of variation and sensitivity for Irisin were lower than 5.1% and 8.1%, respectively. The ELISA assays of Irisin had a sensitivity of <78 pg/mL.

The Kolmogorov-Smirnov Z test was applied to the data to test for normality. An analysis of variance was used to assess the significance of treatment and gender effects. The critical value for significance was set at P =0.05. Results were presented as mean ± SE.

 

Results and Discussion

The effects of the feeding methods on nesfatin-1 levels were significant, but the pattern of the effects differed by gender (Figure 1). Average effects of gender on nesfatin-1 were not detectably different. For the male turkeys, nesfatin-1 levels differed (P <0.05), with the highest levels in T3 (1.24 ± 0.2 ng/ml) and lowest levels in T2 (0.41 ± 0.1 ng/ml) with T1 being intermediate (0.76 ± 0.1 ng/ml). The difference between T2 and T3 was significant, whereas T1 was not significantly different from the other treatments. In contrast, the nesfatin-1 levels of female turkeys in T2, T3, and T1 were 1.18 ± 0.3 ng/ml, 1.32 ± 0.1 ng/ml, and 0.53 ± 0.07 ng/ml, respectively. The nesfatin-1 level of female turkeys that had been subjected to T3 was significantly higher than those that were subjected to T1.

Effects of feeding methods on irisin levels were significant and, as with nesfatin-1, the pattern of effects differed by gender (Figure 2). For the male turkeys, the highest levels of irisin were found in T3 (607.54 ± 24.1 pg/ml) and significantly lower levels T2 (188.39 ± 1.8 pg/ml) with T1 again being intermediate (575.93 ± 42.5 pg/ml), but not different from T3. In contrast, the irisin levels of female turkeys were highest in T1 (603.20 ± 42.2) and lower in T2 (241.42 ± 18.4) and T3 (399.29 ± 21.5 pg/ml). Thus, the irisin levels were depressed for poults in T2 as opposed to those in T1 and T3. The irisin levels found in male turkeys were on average only slightly higher than those found in females.

The hypothalamus plays an important role in the brain as the production site of food intake regulatory factors. More importantly, this area integrates the peripheral and central signalling factors to regulate food intake and long-term bodyweight (Çatli et al., 2014). The nesfatin-1 neuropeptide is a signal that controls appetite in rodents, humans, and fish, resulting in reduced food intake, and can pass through the blood-brain barrier (Price et al., 2007). Likewise, nesfatin-1 has physiological connections at the central nervous system level when regulating nutrient uptake and energy homeostasis in pigs (Varricchio et al., 2014) and rats (Wernecke at al., 2014). Plasma nesfatin-1 levels have been shown to rise as the weight increases (Aydin, 2013; Mirzaei et al., 2014). However, in the current study, the plasma nesfatin-1 levels of the turkeys fed with pasture were higher than those of T1. The turkeys that could access pasture also showed a marked reduction of growth rate at eight weeks, with only the T3 group showing full recovery to the level of T1 by the 16th week (Inci et al., 2020). Haghshenas et al. (2014) reported that exercising would be likely to decrease nutrient intake, weight gain and fat deposition by increasing nesfatin-1 levels. In a study investigating the serum nesfatin-1 levels in patients with disease-related weight loss, it was found that nesfatin-1 levels were lower in the patients with weight loss compared with those with no weight loss, suggesting that weight loss may lower serum nesfatin-1 levels (Cetinkaya et al., 2013). Peripheral concentrations of nesfatin-1 have been found to be significantly negatively correlated with body fat ratio, body fat weight, and blood sugar (Tsuchiya et al., 2010). Significant relationships between fat percentage and circulating nesfatin-1 were observed in obese and morbidly obese subjects (Mirzaei et al., 2014). In obese subjects, with lower nesfatin-1 concentrations, calorie, carbohydrate and protein intakes were even higher, also implying a relationship between nesfatin-1, food consumption and body composition. Further, there may be a feedback mechanism in which the composition of the diet affects the circulating level of nesfatin-1 (Mohan et al., 2014).

Despite these physiological effects in a variety of species, nesfatin-1 expression and physiology have not been studied thoroughlt in birds. Banerjee and Chaturvedi (2015) reported the localization and expression of nesfatin-1 in the testes, ovaries and shell glands of Coturnix coturnix japónica. They emphasized its role in regulating reproduction, and stated that the relationship between appetite control and feed intake through energy balance was important. In the present study, circulating (plasma) nesfatin-1 levels were determined in turkeys fed with various methods. In addition, it was found that plasma nesfatin-1 levels were gender independent (Li et al., 2010). The difference in nesfatin-1 levels between male and female turkeys was found to be non-significant (P =0.10).

Irisin secretion by skeletal muscle cells is induced by exercise in mice and humans, and mildly increased irisin levels in the blood cause an increase in energy expenditure in mice without additional activity or food intake (Böstrom et al., 2012). This increase was from irisin, which caused browning of white adipose tissue and increased metabolism. In T3 irisin levels were high, presumably because of their increased level of physical activity in the more novel environment. However, the heaviest and presumably most sedentary turkeys in this study were in T1 (Inci et al., 2020), and this group had high levels of irisin levels in both males and females. Thus, another explanation could be that these birds had a greater amount of body fat because 28% of the circulating irisin was secreted from adipose tissue (Roca-Rivada et al., 2013). This observation is supported by Stengel et al. (2009), who found that circulating irisin levels in obese individuals were higher than those in individuals with normal weight.

Previous studies have not found a relationship between gender and irisin levels in obese people (Lopez-Legarrea et al., 2014; Blüher et al., 2014). However, in this study the difference between male and female poults in irisin levels bordered on being significant (P =0.054).

 

Conclusions

The feeding methods imposed in this study affected the levels of nesfatin-1 and irisin, with some indication of an interaction between feeding method and gender. Curiously, the hybrid system in which pasture was supplemented with concentrate feed did not consistently produce results that were intermediate between the two extreme feeding methods. However, detailed studies are needed to understand the mechanisms of action of nesfatin-1 and irisin in poultry and whether they can affect animal health and the balance between feed consumption and fattening performance.

 

Acknowledgements

The authors would like to thank Central Laboratory Research and Application Centre, Bingol University

 

Authors' Contributions

HI and FC contributed to the project idea, design and execution of the study. FC and HI were in charge of laboratory analyses. TA and CF were responsible for supervising and writing the manuscript.

 

Conflict of Interest Declaration

The authors declare that there is no conflict of interests regarding the publication of this manuscript.

 

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Submitted 25 March 2020
Accepted 19 November 2020
Published 3 March 2021

 

 

# Corresponding author: hakaninci2565@hotmail.com

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