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Growth in pigs is regulated in large part by the brain neuroendocrine growth hormone (GH)-insulin-like growth factors (IGFs) axis [1]. The complex neuroendocrine control of GH release has been extensively reviewed [2,3]. In essence, the chief hypothalamic regulators of GH release are growth hormone releasing hormone (GHRH) and somatostatin (SS), which are subject to modulation by other hypothalamic peptides and by complex networks of neurotransmitter neurons. GHRH is able not only to stimulate pituitary GH secretion but also promote hypothalamic SS output£¬thus starting an autoregulatory circuit, whereas SS inhibits both GH release from the pituitary gland and GHRH secretion from the hypothalamus.
The inhibiting action of SS may provide an alternative means of accelerating growth because the 14 or 28 amino acid residuals of SS containing an S-S bond are potent inhibitors of endogenous GH secretion [1]. One of the more elegant techniques is represented by the active or passive immunization of animals against endogenous regulatory peptides, for instance, SS, to immunoneutralize them [1,4,5]. In fact, the application of this method in endocrinology has proven to be feasible and has provided remarkable success in some tests with rats£¬sheep, and fish [5¨C8]. However, the growth-promoting effects of anti-SS require further studies, as the results obtained to date provide reasons for optimism with regard to the application of this methodology for the examination of pig growth physiology.
CS is an agent that works as a specific inhibitor of SS in animal production to affect the endocrine system and improve the growth rate of fish, piglets, and finishing pigs [8¨C10]. Thus, CS may become a new candidate as a growth-promoter for pigs. Previous experiments involving rats, sheep, fish, and piglets have demonstrated that CS increases GH secretion [5¨C7,9,11,12]. The increase in GH secretion is possibly due to the decreasing levels of SS in the tissue and hypothalamus in response to the action of CS. The production of IGF-I depends on the actions of GH. IGF-I produced by the liver and other tissues is considered to be the prime effector of GH actions on growth and development. IGF-I produced by the liver is secreted into the circulation and has an endocrine action on target tissues [13,14]. In addition, IGF-I is also produced in most extrahepatic tissues and can function as an autocrine and/or paracrine growth stimulator [13,14]. The biological actions of IGF-I are mediated mainly through the IGF-I receptor (IGF-IR), and partly through the insulin receptor (IR) [15]. Furthermore, IGF binding proteins (IGFBPs) are important modulators of the biological actions of IGF [16]. However, there is no information about continuous long-term CS supplementation on the secretion and gene expression of the IGF system in any mammalian in vivo system.
CS, as a novel growth promoter, is affected in animals by many factors: species of the animal, feeding time, feeding dosage, and chemical stability. Low doses of CS increase the average daily weight gain (ADG) and the average daily feed intake (ADFI) and higher doses of CS have no effect on ADG and ADFI in piglets and finishing pigs.12,13 Moreover, CS supplementation reduces back-fat thickness.13 in vitro study that CS is a reducing aminothiol, which has antioxidant capacity and increases embryo development.20  It can stimulate intracellular glutathione (GSH) production, 21,22 which could protect cells against thiol-derived peroxide. GSH acts as an oxidizable substrate of GSH-Px and as a direct scavenging agent.23 Little information, however, is known on the effects of chronic CS supplementation in meat quality, antioxidation, and carcass characteristics in finishing pigs. We have tested the hypothesis that chronic CS supplementation may affect carcass characteristics, meat quality, and antioxidant status in finishing pigs. In addition, in order to explore the mechanism responsible for the growth-promoting effect of CS supplementation, we have also tested the hypothesis that chronic CS supplementation may affect serum IGF-I concentrations and IGF-I, IGF-IR, IGFBP-3, and IR mRNA levels in different tissues of finishing pigs.
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