RESPONSES OF BROILER CHICKENS FED BETAINE HYDROCHLORIDE SUPPLEMENTATION UNDER DEXAMETHASONE INDUCED STRESS CONDITION

Project Abstract

This study aimed to investigate the responses of broiler chickens when fed betaine hydrochloride supplementation under dexamethasone-induced stress conditions. Dexamethasone, a synthetic glucocorticoid, was used to induce stress in the broiler chickens, while betaine hydrochloride was supplemented in their diet to evaluate its potential protective effects. The experiment was conducted using a total of 120 broiler chickens, which were divided into four groups Group 1 (control), Group 2 (betaine supplementation only), Group 3 (dexamethasone-induced stress), and Group 4 (betaine supplementation + dexamethasone-induced stress). Various parameters were measured to assess the physiological and biochemical responses of the broiler chickens to the different treatments. These parameters included body weight gain, feed intake, feed conversion ratio, serum cortisol levels, antioxidant enzyme activities, and histopathological changes in the liver and bursa of Fabricius. The results indicated that dexamethasone-induced stress negatively impacted the growth performance of the broiler chickens, as evidenced by reduced body weight gain and feed intake, along with an increased feed conversion ratio. However, the group that received betaine hydrochloride supplementation along with dexamethasone-induced stress showed improvements in these parameters compared to the stress-only group. The betaine supplementation helped mitigate the negative effects of stress on the growth performance of the broiler chickens. Furthermore, the serum cortisol levels were lower in the betaine supplementation group under stress conditions, indicating a potential stress-reducing effect of betaine. In terms of antioxidant enzyme activities, the betaine supplementation group exhibited higher levels of superoxide dismutase (SOD) and catalase, indicating enhanced antioxidant defense mechanisms. Histopathological analysis revealed that betaine supplementation ameliorated the liver and bursa of Fabricius damage induced by dexamethasone-induced stress. Overall, the findings suggest that betaine hydrochloride supplementation has protective effects against dexamethasone-induced stress in broiler chickens. The supplementation improved growth performance, reduced serum cortisol levels, enhanced antioxidant enzyme activities, and mitigated histopathological changes in vital organs. These results highlight the potential of betaine hydrochloride as a nutritional supplement to alleviate stress and improve the welfare of broiler chickens in intensive production systems.

Project Overview

<p> </p><p>It is estimated that world food consumption will double by 2050 as more developing nations improve their economic status and per capital meat consumption increase (Godfray <em>et al</em>., 2010). This places an increasing pressure on animal producers especially poultry farmers to maximize output levels of their animals to meet this growing demand. Physiological stress is one of many concerns facing the modern broiler producer. The term stress is very familiar to most researchers, but there is no universal definition for stress. When a stressor is actually causing a negative impact on the well-being of an animal, this can be defined as distress (Moberg, 2000). Another broader definition states that stress is any biological response elicited when an animal perceives a threat to its homeostasis (Moberg, 2000). Extremes of ambient temperature is an important stressor that confronts poultry in many regions of the world and large economic losses occur because of mortality and decreased production (Altan <em>et al</em>., 2000).</p><p>The thermoneutral zone for poultry is 18°C–24°C in the tropics and 12°C–26°C in the temperate zones, but this often gets exceeded in the tropics, resulting in heat stress (Holik, 2009; Dei and Bumbie, 2011). When the hypothalamic-pituitary-adrenocortical axis is activated, the hypothalamus produces corticotrophin-releasing factor, which in turn stimulates the pituitary to release adrenocorticotropic hormone (ACTH) (Mormède <em>et al.,</em>&nbsp;2007). Secretion of ACTH causes the cells of the adrenal cortical tissue to proliferate and to secrete corticosteroids. The main active hormone of the axis is cortisol in cattle, sheep, pig, mink, fox and fish, and corticosterone (CS) in birds and rodents (Mormède <em>et al.,</em>&nbsp;2007). These are cholesterol-derived steroids synthesized in the fascicular zone of the adrenal cortex under the control of the pituitary hormone. ACTH is synthesized by specialized cells (corticotrophs) of the anterior pituitary gland (Mormède <em>et al.,</em>&nbsp;2007).The production of glucocorticoids is increased by stress; therefore, corticosterone can be used as a biomarker of stress in poultry.</p><p>In chickens, adrenal corticosteroids are secreted shortly after exposure to stress and elevated levels of plasma glucocorticoids have been used as an index of the response to stress in poultry (Siegel, 1995). By elevating circulatory corticosteroids and decreasing thyroid activity, heat stress impairs broiler performance, especially <a target="_blank" rel="nofollow" href="https://www.modishproject.com/assessment-of-effectiveness-of-educational-radio-broadcasting-for-adult-literacy-in-lagos-state-nigeria/">adult birds</a>, because the ability to dissipate heat decreases with age (Mahmoud <em>et al</em>., 2014). Drastic decline in feed intake occurring in heat-stressed birds is a physiological response to minimize intrinsic<a target="_blank" rel="nofollow" href="https://www.modishproject.com/bread-using-blend-wheat-flour/">&nbsp;heat production</a>. It is aimed at maintaining thermal homeostasis, thus decreasing feed efficiency, live weight gain, and survival rates (Faria-Filho <em>et al</em>., 2007). Lower breast-meat yield and higher carcass-fat deposition are the other deleterious effects of heat stress that lower the economic value of broiler carcasses (Geraert <em>et al</em>., 1996; Ain-Baziz<em>&nbsp;et al</em>., 1996). Corticosterone has an indirect role in lipid metabolism bycausing the rate of fat deposition to increase in poultry (Jiang <em>et al</em>., 2008; Yuan <em>et al</em>., 2008). Glucocorticoid hormone secretion also has implications for mineral metabolism, thus corticosteroids have been directly implicated in the development of osteoporosis in stressed animals (Siegel and Latimer, 1970). It has also been shown that glucocorticoids support the action of catecholamines, which have been shown to increase urinary calcium and sodium excretion (Fink and Brody, 1978).</p><p>Corticosteroids have been shown to inhibit several immune system functions in various species, as demonstrated in depressed number of circulating lymphocytes, which results in an increase in the ratio of circulating heterophils to lymphocytes, the most recognizable symptom of stress in poultry (Siegel, 1995). Regression of the thymus, bursa, and spleen has also been demonstrated in chickens after corticosterone or ACTH administration <em>(</em>Puvadolpirod and Thaxton, 2000a).</p><p>Similarly, synthetic glucocorticoid dexamethasone administration mimics the adverse effects of increased corticosterone. Dexamethasone (doses ranging from 0.2 to 4.0 mg/kg) has been used as an immune suppressive agent (Fowles <em>et al</em>., 1993), mediator of prenatal stress (Maccari <em>et al</em>., 2003) and to induce oxidative stress in laying hens (El-Habbak <em>et al</em>. 2005) and cockerels (Eid <em>et</em>&nbsp;<em>al</em>., 2006). Aengwanich (2007) demonstrated that synthetic glucocorticoid; dexamethasone indoses of up to 6 mg/kg in their diets had many effects on broilers like internal glucocorticoid.</p><p>Certain feed additives (selenium, vitamins C and E, α-lipoic acid, α-tocopherol, prebiotics and probiotics) enhance performance in heat-stressed broilers (Ghazi Harsini <em>et al</em>., 2012; Hamano, 2012; Imik <em>et al</em>., 2012; Khan <em>et al</em>., 2012; Sandhu <em>et al</em>., 2012; Sohail <em>et al</em>., 2012). Betaine, a methyl group donor, functions in <a target="_blank" rel="nofollow" href="https://www.modishproject.com/ethanol-leaf-extract-of-irvingia-gabonensis-ororke-baill-mitigates-sodium-arsenite-induced-lipid-profile-derangements-in-wistar-rats/">lipid metabolism</a>&nbsp;by stimulating oxidative catabolism of fatty acids through carnitine synthesis. Betaine is also an organic osmolyte and does not interfere with enzyme function or upset metabolism (Simon, 1999). As an osmolyte, betaine may have a stabilizing function on cells subjected to osmotic stressors, such as in the case of coccidiosis infection (Klasing <em>et al</em>., 2002) by regulating the water balance, resulting in the stability of tissue metabolism especially in the gastrointestinal tract (Lipinski <em>et al.,</em>&nbsp;2012). Dietary supplementation of betaine presumably reduces the requirement for other methyl-group donors, such as methionine and choline (Siljander-Rasi <em>et al</em>., 2003). Florou-Paneri <em>et al</em>. (1997) showed that between 30 and 80 percent of supplemental methionine can be substituted by betaine without negative effects on performance. As a feed additive, betaine is most commonly added to animal diets as anhydrous betaine; betaine monohydrate, and betaine hydrochloride (Kidd <em>et al</em>., 1997; Eklund <em>et al</em>., 2005). Within the body, betaine is synthesized from choline (Sakomura <em>et al</em>., 2013).</p><br> <br><p></p>