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. Author manuscript; available in PMC: 2022 Nov 1.
Published in final edited form as: Alcohol Clin Exp Res. 2021 Sep 30:10.1111/acer.14719. doi: 10.1111/acer.14719

Figure 2: Intravenous ghrelin administration alters the circulating metabolite profile.

Figure 2:

Serum metabolite profiles were analyzed from repeated serum samples collected during each of the four sessions (see Figure 1). When comparing area under the curve values using linear mixed-effect models, significant differences between ghrelin and placebo infusions were seen in both the intravenous (IV) alcohol self-administration (ASA) experiment and the IV alcohol clamp (AC) experiment in levels of cortisol (FRD corrected q-value = 0.0003, and <0.0001, respectively), corticosterone (q = 0.0202, and <0.0001, respectively), and glycochenodeoxycholic acid (q = 0.0375, and 0.0013, respectively). Furthermore, during the IV-ASA experiment, significant differences between ghrelin and placebo infusions were seen also in the levels of cortisone (q = 0.0352), fatty acids (FA) 18:1 (q = 0.0406) and FA 18:3 (q = 0.0320), and hippuric acid (q = 0.0112). However, these metabolites were not significantly altered in the IV-AC experiment (cortisone q = 0.5237, FA 18:1 q = 0.9698, FA 18:3 q = 0.9843, and hippuric acid q = 0.9886). Moreover, in the IV-AC experiment, significant differences between the ghrelin and placebo infusions were seen in levels of glycocholic acid (q < 0.0001), and phenylalanine (q = 0.0458). However, these metabolites were not significantly altered in the IV-ASA experiment (glycocholic acid q = 0.3197, and phenylalanine q = 0.9259). Mean ion abundance and standard error of mean are shown for each measurement point. Abbreviations: BrAC=Breath Alcohol Concentration; infusion=continuous infusion of ghrelin or placebo; IV=Intravenous; IV-ASA=IV Alcohol Self-Administration; IV-A=IV Alcohol Clamp; LD=Loading Dose.