Background: This study aimed to investigate the mechanisms by which Citrus aurantium honey modulates gastrointestinal motility, inflammation, and barrier function using network pharmacology and Drosophila melanogaster models.
Methods: Ultra-high-performance liquid chromatography coupled with Q Exactive high-field mass spectrometry (UHPLC-Q Exactive HF-MS) characterized the chemical profile. Network pharmacology predicted targets and enriched pathways, and molecular docking validated core component–target binding. In lipopolysaccharide (LPS)-induced Drosophila intestinal injury models, functional assays (fecal excretion, intestinal transit, barrier integrity) and mechanistic analyses (reactive oxygen species [ROS] levels, TORC1 pathway–related protein/gene expression) were performed.
Results: Network pharmacology revealed 17 key targets enriched in calcium signaling, cAMP/cGMP-PKG, and neuroactive ligand–receptor pathways. In Drosophila, honey dose-dependently (0.25% < 0.5% < 1%) enhanced intestinal motility (increased volume of stool and shorter transit time) and reduced inflammation (reduced ROS levels and improved barrier integrity, p < 0.01). Mechanistically, honey inhibited TORC1 overactivation by reducing 4E-BP phosphorylation and regulating Thor/Nprl2 expression.
Conclusions: C. aurantium honey exerts gastrointestinal effects via a “multi-component, multi-target” mechanism. It modulates smooth muscle contraction through calcium/cAMP/cGMP pathways and alleviates inflammation by suppressing TORC1 signaling, highlighting its potential as a dietary intervention for dysmotility and inflammation.
| [1] |
Lacy BE, Weiser K. Gastrointestinal motility disorders: an update. Dig Dis. 2006; 24(3–4): 228-242.
|
| [2] |
Mao L, Liang Q, Wang L, et al. Effects of Pingwei capsule on gastrointestinal motility in a rat model of functional dyspepsia based on the brain–gut axis. Chin J Pharmacol Clin Ther. 2019; 35(5): 84-90.
|
| [3] |
Guo X, Xu Y. The key ingredient acacetin in Weishu decoction alleviates gastrointestinal motility disorder based on network pharmacology analysis. Mediat Inflamm. 2021; 2021:5265444.
|
| [4] |
Zhang Y, Wang L, Zhang Z. Effect of Huazhuo Jiedu Shugan formula on gastrointestinal motility in rats with liver-qi stagnation type functional dyspepsia based on the brain–gut axis. Chin J Gerontol. 2023; 43(23): 5805-5809.
|
| [5] |
Sperber AD, Bangdiwala SI, Drossman DA, et al. Worldwide prevalence and burden of functional gastrointestinal disorders, results of Rome Foundation Global Study. Gastroenterology. 2021; 160(1): 99-114.e3.
|
| [6] |
Brenner DM, Domínguez-Muñoz JE. Differential diagnosis of chronic diarrhea: an algorithm to distinguish irritable bowel syndrome with diarrhea from other organic gastrointestinal diseases, with special focus on exocrine pancreatic insufficiency. J Clin Gastroenterol. 2023; 57(7): 663-670.
|
| [7] |
Bosman M, Bosman MHMA, Weerts ZZRM, et al. The socio-economic impact of irritable bowel syndrome: an analysis of direct and indirect health care costs. Clin Gastroenterol Hepatol. 2023; 21(10): 2660-2669.
|
| [8] |
Wang R, Xu Y, Xu C, et al. Research progress on the mechanism of gastrointestinal motility disorders in inflammatory bowel disease. Chin J Gastroenterol. 2021; 26(12): 748-751.
|
| [9] |
Wang M, Fu R, Xu D, et al. Traditional Chinese medicine: a promising strategy to regulate the imbalance of bacterial flora, impaired intestinal barrier and immune function attributed to ulcerative colitis through intestinal microecology. J Ethnopharmacol. 2024; 318(Pt A):116879.
|
| [10] |
Liu Y, Li BG, Su YH, et al. Potential activity of traditional Chinese medicine against ulcerative colitis: a review. J Ethnopharmacol. 2022; 289:115084.
|
| [11] |
He W, Li Y, Liu M, et al. Citrus aurantium L. and its flavonoids regulate TNBS-induced inflammatory bowel disease through anti-inflammation and suppressing isolated jejunum contraction. Int J Mol Sci. 2018; 19(10):3057.
|
| [12] |
Gao M, Yang W. Effects of Citrus aurantium L. on gastrointestinal motility and gastric cancer cell proliferation. Cancer Biother Radiopharm. 2023; 38(2): 111-115.
|
| [13] |
He W, Liu M, Li Y, et al. Flavonoids from Citrus aurantium ameliorate TNBS-induced ulcerative colitis through protecting colonic mucus layer integrity. Eur J Pharmacol. 2019; 857:172456.
|
| [14] |
Zhu J, Tong H, Ye X, et al. The effects of low-dose and high-dose decoctions of Fructus aurantii in a rat model of functional dyspepsia. Med Sci Monit. 2020; 26:e919815.
|
| [15] |
Yi S, Zhang G, Liu M, et al. Citrus honey ameliorates liver disease and restores gut microbiota in alcohol-feeding mice. Nutrients. 2023; 15(5):1078.
|
| [16] |
Peller CR, Bacon EM, Bucheger JA, Blumenthal EM. Defective gut function in drop-dead mutant Drosophila. J Insect Physiol. 2009; 55(9): 834-839.
|
| [17] |
Tang R. Research on the anti-aging activity and molecular mechanism of Lycium barbarum polysaccharides based on Drosophila model. Master's Thesis, Northwest University; 2019.
|
| [18] |
Zhou Y, Liu ZL, Chen YC, et al. Effects of extracts from Trichosanthes kirilowii, Carthamus tinctorius, Ligusticum chuanxiong and Chrysanthemum morifolium on gut immunity of Drosophila melanogaster induced by oxidative stress. Chin Tradit Herb Drug. 2014; 45(15): 2194-2200.
|
| [19] |
Xia ZK, Yin LZ, Zheng YH, et al. Effect of Sargassum fusiforme polysaccharide on antioxidant activity and lifespan of Drosophila. Pharm Biotechnol. 2018; 25(2): 130-134.
|
| [20] |
Sanders KM, Koh SD, Ro S, Ward SM. Regulation of gastrointestinal motility—insights from smooth muscle biology. Nat Rev Gastroenterol Hepatol. 2012; 9(11): 633-645.
|
| [21] |
Wank SA. G protein-coupled receptors in gastrointestinal physiology. I. CCK receptors: an exemplary family. Am J Phys. 1998; 274(4 Pt 1): G607-G613.
|
| [22] |
Bonvento G, Bolaños JP. Astrocyte-neuron metabolic cooperation shapes brain activity. Cell Metab. 2021; 33(8): 1546-1564.
|
| [23] |
Fanibunda SE, Deb S, Maniyadath B, et al. Serotonin regulates mitochondrial biogenesis and function in rodent cortical neurons via the 5-HT(2A) receptor and SIRT1-PGC-1α axis. Proc Natl Acad Sci USA. 2019; 116(22): 11028-11037.
|
| [24] |
Guzel T, Mirowska-Guzel D. The role of serotonin neurotransmission in gastrointestinal tract and pharmacotherapy. Molecules. 2022; 27(5):1680.
|
| [25] |
Ellaithy A, Gonzalez-Maeso J, Logothetis DA, Levitz J. Structural and biophysical mechanisms of class C G protein-coupled receptor function. Trends Biochem Sci. 2020; 45(12): 1049-1064.
|
| [26] |
Gurevich EV, Gainetdinov RR, Gurevich VV. G protein-coupled receptor kinases as regulators of dopamine receptor functions. Pharmacol Res. 2016; 111: 1-16.
|
| [27] |
Ippolito M, de Pascali F, Inoue A, Benovic JL. Phenylalanine 193 in extracellular loop 2 of the β(2)-adrenergic receptor coordinates β-Arrestin interaction. Mol Pharmacol. 2022; 101(2): 87-94.
|
| [28] |
Hill CS, Treisman R. Transcriptional regulation by extracellular signals: mechanisms and specificity. Cell. 1995; 80(2): 199-211.
|
| [29] |
Liu HN, Ohya S, Furuzono S, Wang J, Imaizumi Y, Nakayama S. Co-contribution of IP3R and Ca2+ influx pathways to pacemaker Ca2+ activity in stomach ICC. J Biol Rhythm. 2005; 20(1): 15-26.
|
| [30] |
Zhang K, Xu Y, Zheng Y, et al. Bifidobacterium pseudolongum-derived bile acid from dietary carvacrol and thymol supplementation attenuates colitis via cGMP-PKG-mTORC1 pathway. Adv Sci. 2024; 11(43):e2406917.
|
| [31] |
Wang JY, Duan WQ, Du H, et al. Exploring the mechanism of astragaloside IV in treating diabetic nephropathy based on network pharmacology and molecular docking. Shanxi. J Tradit Chin Med. 2025; 41(7): 61-64+71.
|
| [32] |
Dong BH, Peng Y, Jiang YX, et al. Analysis of the processing mechanism of “salt-processing enhancing efficacy” in Wuzi Yanzong pills by UPLC-Q-TOF-MS combined with network pharmacology and molecular docking. Chin J Pharmacol Clin Ther. 2023; 39(12): 15-24.
|
| [33] |
Wu L, Li GY, Yan YP, et al. Protective effect of thymoquinone on chemically induced ulcerative colitis. J Hefei Univ Technol (Nat Sci Ed). 2023; 46(6): 849-852.
|
| [34] |
Du P, Paskaranandavadivel N, Angeli TR, Cheng LK, O'Grady G. The virtual intestine: in silico modeling of small intestinal electrophysiology and motility and the applications. Wiley Interdiscip Rev Syst Biol Med. 2016; 8(1): 69-85.
|
| [35] |
Xie Z, Rose L, Feng J, et al. Enteric neuronal Piezo1 maintains mechanical and immunological homeostasis by sensing force. Cell. 2025; 188(9): 2417-2432.e19.
|
| [36] |
Zheng Z, Tang J, Hu Y, Zhang W. Role of gut microbiota-derived signals in the regulation of gastrointestinal motility. Front Med (Lausanne). 2022; 9:961703.
|
| [37] |
Chang L. The role of stress on physiologic responses and clinical symptoms in irritable bowel syndrome. Gastroenterology. 2011; 140(3): 761-765.
|
| [38] |
Thomas EA, Carson MJ, Neal MJ, Sutcliffe JG. Unique allosteric regulation of 5-hydroxytryptamine receptor-mediated signal transduction by oleamide. Proc Natl Acad Sci USA. 1997; 94(25): 14115-14119.
|
| [39] |
Huang GY, Kim JJ, Reger AS, et al. Structural basis for cyclic-nucleotide selectivity and cGMP-selective activation of PKG I. Structure. 2014; 22(1): 116-124.
|
| [40] |
Deshpande R, Lee B, Qiao Y, Grewal SS. TOR signalling is required for host lipid metabolic remodelling and survival following enteric infection in Drosophila. Dis Model Mech. 2022; 15(5):dmm049551.
|
| [41] |
Strilbytska OM, Storey KB, Lushchak OV. TOR signaling inhibition in intestinal stem and progenitor cells affects physiology and metabolism in Drosophila. Comp Biochem Physiol B Biochem Mol Biol. 2020; 243–244:110424.
|
| [42] |
Ouweneel AB, Thomas MJ, Sorci-Thomas MG. The ins and outs of lipid rafts: functions in intracellular cholesterol homeostasis, microparticles, and cell membranes: thematic review series: biology of lipid rafts. J Lipid Res. 2020; 61(5): 676-686.
|
| [43] |
Bernard C, Carotenuto AR, Pugno NM, Fraldi M, Deseri L. Modelling lipid rafts formation through chemo-mechanical interplay triggered by receptor-ligand binding. Biomech Model Mechanobiol. 2024; 23(2): 485-505.
|
| [44] |
Snape WJ Jr. Role of motility measurements in managing upper gastrointestinal dysfunction. Gastroenterologist. 1998; 6(1): 44-59.
|
| [45] |
Luo D, Huang Z. Naringin mitigates LPS-induced intestinal barrier injury in mice. Food Funct. 2023; 14(3): 1617-1626.
|
| [46] |
Gu YF, Chen YP, Jin R, Wang C, Wen C, Zhou YM. Dietary chitooligosaccharide supplementation alleviates intestinal barrier damage, and oxidative and immunological stress in lipopolysaccharide-challenged laying hens. Poult Sci. 2022; 101(4):101701.
|
| [47] |
Xi JM. Functional study of Nprl2 gene in Drosophila Gastrointestinal aging model. Master's Thesis, Yangzhou University; 2020.
|
| [48] |
Yu JB, Zhu JY, Mei WY, et al. Research progress on the mechanism of Fructus aurantii and its active components in regulating gastrointestinal motility. Chin J Exp Tradit Med Formul. 2024; 30(10): 290-298.
|
| [49] |
Tseng CH, Wu CY. From dysbiosis to longevity: a narrative review into the gut microbiome's impact on aging. J Biomed Sci. 2025; 32(1): 93.
|
| [50] |
Kang P, Ryu KH, Lee JM, Kim HK, Seol GH. Endothelium- and smooth muscle-dependent vasodilator effects of Citrus aurantium L. var. amara: focus on Ca(2+) modulation. Biomed Pharmacother. 2016; 82: 467-471.
|
| [51] |
Markowiak-Kopeć P, Śliżewska K. The effect of probiotics on the production of short-chain fatty acids by human intestinal microbiome. Nutrients. 2020; 12(4):1107.
|
| [52] |
Barron JT, Bárány M, Gu L, Parrillo JE. Metabolic fate of glucose in vascular smooth muscle during contraction induced by norepinephrine. J Mol Cell Cardiol. 1998; 30(3): 709-719.
|
| [53] |
Wang T, Xu YQ, Yuan YX, et al. Succinate induces skeletal muscle fiber remodeling via SUCNR1 signaling. EMBO Rep. 2021; 22(6):e53027.
|
| [54] |
Stevens Y, de Bie T, Pinheiro I, Elizalde M, Masclee A, Jonkers D. The effects of citrus flavonoids and their metabolites on immune-mediated intestinal barrier disruption using an in vitro co-culture model. Br J Nutr. 2022; 128(10): 1917-1926.
|
| [55] |
Li J, Xie S, Chen M, et al. Panose prevents acute-on-chronic liver failure by reducing bacterial infection in mice. J Clin Invest. 2025; 135(14):e184653.
|
| [56] |
Yang WS, Lee SR, Jeong YJ, et al. Antiallergic activity of ethanol extracts of Arctium lappa L. undried roots and its active compound, oleamide, in regulating FcεRI-mediated and MAPK signaling in RBL-2H3 cells. J Agric Food Chem. 2016; 64(18): 3564-3573.
|
| [57] |
Bauset C, Lis-Lopez L, Coll S, et al. SUCNR1 mediates the priming step of the inflammasome in intestinal epithelial cells: relevance in ulcerative colitis. Biomedicine. 2022; 10(3):532.
|
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2026 The Author(s). Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences.