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  • AZD 3965 australia It has been suggested that the presence o


    It has been suggested that the presence of nutrient-sensing receptors and their natural ligands originating from different metabolic pathways in farm animals, are related to the critical outcome of metabolic-derived diseases in cattle (Mielenz, 2017). Thus, current article aimed to review the most recently accumulated evidence supporting the potential role of fatty acids, hydroxycarboxylic acids, and their receptors as the missing link of immunometabolic diseases in cattle.
    Fatty acids
    Hydroxycarboxylic acid
    Introduction In the past 20 years, it has become clear that GPCR ligands include not only traditional hormones and neurotransmitters but also ions and other endogenous molecules. In this chapter, we focus on a recently discovered GPCR family with affinity for several intermediates of energy metabolism. These metabolite ligands are all hydroxy-carboxylic acids (HCAs), hence the novel nomenclature for this receptor family: HCA receptors (Ahmed et al., 2009b, Offermanns 2011). HCA1 (GPR81) is endogenously activated by lactate, HCA2 (GPR109A) by 3-hydroxy-butyrate, and HCA3 (GPR109B) by 3-hydroxylated β-oxidation intermediates, especially 3-hydroxy-octanoic AZD 3965 australia (Ahmed et al., 2009a, Cai et al., 2008, Liu et al., 2009, Taggart et al., 2005). All three receptors are predominantly expressed in adipose tissue, where they couple to Gi proteins (Ahmed et al., 2009b). Activation of the receptors has an antilipolytic effect. Discovery of the endogenous HCA ligands has increased our understanding of the (patho)physiological roles of their receptors and opens new avenues for research and drug discovery. Of the HCA family, HCA2 is most extensively studied, as it is the target of the antidyslipidemic drug nicotinic acid (or niacin; Soga et al., 2003, Tunaru et al., 2003, Wise et al., 2003). Nicotinic acid has been used since the 1950s (Altschul et al., 1955) and is still the most efficacious drug approved to raise HDL cholesterol plasma levels (Carlson, 2005). In HCA2 knockout mice, the antilipolytic and triglyceride lowering effects of nicotinic acid are abolished (Tunaru et al., 2003). Skin flushing, the major nicotinic acid side effect, was also shown to be receptor dependent (Benyó et al., 2006). Separating this side effect from the therapeutic effects of HCA2 ligands is one of the major challenges in this field. In addition, it will be important to analyze the potential of HCA1 and HCA3 as therapeutic targets. This review will summarize current knowledge on the pharmacology and physiology of HCA receptors as well as the recent development of new synthetic ligands of this receptor class.
    Identification and Characterization of HCA Receptors
    Gene Structure and Tissue Distribution
    Physiological and Pharmacological Roles of HCA Receptors
    Receptor Classification with Pharmacological Tools Although nicotinic acid was introduced in man in the 1950s (Altschul et al., 1955), structure–activity relationships for its target(s) were developed much later. Only in the 1980s, Aktories et al., 1980, Aktories et al., 1983 proposed the existence of a specific receptor for nicotinic acid and a related compound, acipimox. Progress being slow, members of the same laboratory explored a few more compounds related to nicotinic acid in a number of receptor assays, using membranes from rat adipocytes and rat spleen (Lorenzen et al., 2001). A few years later, the human HCA2 receptor was cloned (Wise et al., 2003). In that paper, a number of nicotinic acid-like compounds were also tested. As most medicinal chemistry efforts have been directed toward the HCA2 receptor, we will discuss the synthetic ligands for this receptor first, followed by the more restricted information on the HCA3 receptor. To our knowledge, synthetic ligands for the HCA1 receptor have only been reported in the patent literature, which is beyond the scope of this review. Last but not least, antagonists have not been disclosed for any of the HCA receptors, which are currently hampering a full pharmacological characterization of these receptors. A few years ago, we published a review on the then available ligands, largely nicotinic acid-like compounds (Soudijn et al., 2007). The current review does not reiterate that but starts from there and is organized according to chemical classes. We report representative structures of these classes in Fig. 3.