Natural Products and Bioprospecting    2023, Vol. 13 Issue (4) : 29-29     DOI: 10.1007/s13659-023-00390-3
ORIGINAL ARTICLES |
Puerarin alleviates sleep disorders in aged mice related to repairing intestinal mucosal barrier
Qing Tao1, Jinhua Zhang2, Qiao liang1, Shiyu Song1, Shuxia Wang2, Xiaoming Yao2, Qian Gao1, Lei Wang1,3
1. Center for Translational Medicine and Jiangsu Key Laboratory of Molecular Medicine, Medical School, Nanjing University, Nanjing, 210093, Jiangsu, China;
2. Department of Clinical Laboratory, Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Jiangsu Province Academy of Traditional Chinese Medicine, Nanjing, 210028, China;
3. Department of Clinical Laboratory, Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Jiangsu Province Academy of Traditional Chinese Medicine, Nanjing, 210028, China
Download: PDF(2598 KB)   HTML ()  
Export: BibTeX | EndNote | Reference Manager | ProCite | RefWorks    
Abstract  More and more evidence suggests that puerarin, a potential remedy for gut inflammation, may have an ameliorative effect on sleep disturbances. However, the relationship between puerarin and sleep disruption has not been extensively researched. This study aims to explore the role and mechanisms of puerarin in improving sleep disorders. We established a light-induced sleep disorder model in mice and assessed the effects of puerarin on cognitive behavior using open field and water maze tests. Pathological detection demonstrated that sleep disturbances resulted in observable damage to the liver, lung, and kidney. Puerarin reversed multi-organ damage and inflammation. Further, puerarin activated paneth cells, resulting in increased lysozyme and TGF-β production, and stimulating intestinal stem cell proliferation. Puerarin also effectively inhibited the expression of F4/80, iNOS, TNF-α, and IL-1β in the small intestine, while it increased Chil3, CD206, and Arg-1 levels. Moreover, puerarin treatment significantly decreased P-P65, TLR4, Bcl-xl, and cleaved caspase-3 protein levels while increasing barrier protein levels, including ZO-1, Occludin, Claudin 1 and E-cadherin suggesting a reduction in inflammation and apoptosis in the gut. Overall, puerarin diminished systemic inflammation, particularly intestinal inflammation, and enhanced intestinal barrier integrity in mice with sleep disorders. Our findings suggest a potential new therapeutic pathway for sleep disorders.
Keywords Intestinal inflammation      Intestinal mucosal barrier      Light-induced sleep disorder      Puerarin     
Fund:We thank all involved for their participation and technical support. We also thank the Center for Translational Medicine and Jiangsu Key Laboratory of Molecular Medicine, Medical School of Nanjing University and the Department of Clinical Laboratory, Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese medicine, Jiangsu Province Academy of Traditional Chinese Medicine. The authors wish to express their gratitude for the financial support received from the National Key Research and Development Program of China (No: 2020YFC2005300, No: 2021YFC2009101), Open/Independent Project of the Center for Translational Medicine and Jiangsu Key Laboratory of Molecular Medicine, Medical School of Nanjing University, and Jiangsu Province Postgraduate Scientific Research Innovation Project (KYCX22-0183).
Corresponding Authors: Qian Gao,E-mail:qian_gao@nju.edu.cn;Lei Wang,E-mail:wlei@nju.edu.cn     E-mail: qian_gao@nju.edu.cn;wlei@nju.edu.cn
Issue Date: 08 October 2023
Service
E-mail this article
E-mail Alert
RSS
Articles by authors
Qing Tao
Jinhua Zhang
Qiao liang
Shiyu Song
Shuxia Wang
Xiaoming Yao
Qian Gao
Lei Wang
Trendmd:   
Cite this article:   
Qing Tao,Jinhua Zhang,Qiao liang, et al. Puerarin alleviates sleep disorders in aged mice related to repairing intestinal mucosal barrier[J]. Natural Products and Bioprospecting, 2023, 13(4): 29-29.
URL:  
http://npb.kib.ac.cn/EN/10.1007/s13659-023-00390-3     OR     http://npb.kib.ac.cn/EN/Y2023/V13/I4/29
1. Gulia KK, Kumar VM. Sleep disorders in the elderly: a growing challenge. Psychogeriatrics. 2018;18(3):155–65.
2. Cybulski M, et al. Sleep disorders among educationally active elderly people in Bialystok, Poland: a cross-sectional study. BMC Geriatr. 2019;19(1):1–8.
3. Li Q, et al. Obstructive sleep apnea is related to alterations in fecal microbiome and impaired intestinal barrier function. Sci Rep. 2023;13(1):778.
4. Ancoli-Israel S. Sleep and aging: prevalence of disturbed sleep and treatment considerations in older adults. J Clin Psychiatry. 2005;66:24–30.
5. Wagner-Skacel J, et al. Sleep and microbiome in psychiatric diseases. Nutrients. 2020;12(8):2198.
6. Malaivijitnond S. Medical applications of phytoestrogens from the thai herb Pueraria mirifica. Front Med. 2012;6:8–21.
7. Leblanc M-F, Desjardins S, Desgagné A. Sleep problems in anxious and depressive older adults. Psychol Res Behav Manage. 2015;8:161–9.
8. Liu R, et al. Puerarin mitigates symptoms of depression in ovariectomized female rats by regulating hippocampal cAMP-CREB-BDNF signaling pathway. Trop J Pharm Res. 2021;20(7):1403–9.
9. Chiao Y-W, et al. Use of chinese herbal medicines is related to a reduction in depression risk among patients with insomnia: a matched cohort study. Front Neurol. 2021;11:583485.
10. Dai J, et al. Edible plant Jiaosu: manufacturing, bioactive compounds, potential health benefits, and safety aspects. J Sci Food Agric. 2020;100(15):5313–23.
11. Gao LN, et al. Puerarin alleviates depression-like behavior induced by high-fat diet combined with chronic unpredictable mild stress via repairing TLR4-induced inflammatory damages and phospholipid metabolism disorders. Front Pharmacol. 2021;12:767333.
12. Liu X, Huang R, Wan J. Puerarin: a potential natural neuroprotective agent for neurological disorders. Biomed Pharmacother. 2023;162:114581.
13. Fisher JR, et al. Pattern recognition receptors in innate immunity to obligate intracellular bacteria. Zoonoses (Burlington Mass). 2021;1(1):10.
14. Li J, et al. Puerarin improves intestinal barrier function through enhancing goblet cells and mucus barrier. J Funct Foods. 2020;75:104246.
15. Wennberg AM, et al. Sleep disturbance, cognitive decline, and dementia: a review. Semin Neurol. 2017. https://doi.org/10.1055/s-0037-1604351.
16. Chokroverty S. Overview of sleep & sleep disorders. Indian J Med Res. 2010;131(2):126–40.
17. Wershil BK, Furuta GT. Gastrointestinal mucosal immunity. J Allergy Clin Immunol. 2008;121(2):S380–3.
18. Kim YS, Ho SB. Intestinal goblet cells and mucins in health and disease: recent insights and progress. Curr Gastroenterol Rep. 2010;12(5):319–30.
19. Barreto e, Barreto L, et al. Paneth cells and their multiple functions. Cell Biol Int. 2022;46(5):701–10.
20. Luvhengo T, Khan U, Marumo TKJAS. Paneth cells and Lgr5 + intestinal stem cells in Radiation Enteritis. Appl Sci. 2023;13(5):2758.
21. Samanta S. Mechanisms of gastrointestinal pathogenesis and landscape of intestinal immunity, viral, parasitic, bacterial, and fungal infections. 2023, Elsevier, pp. 863–913.
22. Li C, et al. Glycolytic regulation of Intestinal Stem Cell Self-Renewal and differentiation. Cell Mol Gastroenterol Hepatol. 2023;15(4):931–47.
23. Wang C, et al. Dysregulated lung stroma drives emphysema exacerbation by potentiating resident lymphocytes to suppress an epithelial stem cell reservoir. Immunity. 2023;56(3):576–91.
24. Saez A, et al. Pathophysiology of inflammatory bowel disease: Innate Immune System. Int J Mol Sci. 2023;24(2):1526.
25. Wang M, et al. Exercise suppresses neuroinflammation for alleviating Alzheimer’s disease. J Neuroinflamm. 2023;20(1):1–22.
26. Zhu T, et al. Puerarin alleviates vascular cognitive impairment in vascular dementia rats. Front Behav Neurosci. 2021;15:717008.
27. Li S, et al. Flavonoids ameliorate aluminum chloride-induced learning and memory impairments via suppression of apoptosis and oxidative stress in rats. J Inorg Biochem. 2020;212:111252.
28. Mallick BN, Mehta R. Optimum sleep for healthy ageing. In: Sleep and clocks in aging and longevity. Springer, 2023. pp. 129–42.
29. Liu B, et al. Gastrodin improves cognitive dysfunction in REM sleep-deprived rats by regulating TLR4/NF-κB and Wnt/β-Catenin signaling pathways. Brain Sci. 2023;13(2):179.
30. Wang J, et al. Treatment of insomnia based on the mechanism of pathophysiology by acupuncture combined with herbal medicine: a review. Med (Baltim). 2023;102(11):e33213.
31. Lin WL, et al. Using text mining and data visualization approaches for investigating Mental illness from the perspective of traditional chinese medicine. Med (Kaunas). 2023;59(2):196.
32. Lee YD, et al. Melatonin attenuates lipopolysaccharide-induced acute lung inflammation in sleep-deprived mice. J Pineal Res. 2009;46(1):53–7.
33. Irwin MR, et al. Sleep deprivation and activation of morning levels of cellular and genomic markers of inflammation. Arch Intern Med. 2006;166(16):1756–62.
34. Baranwal N, Yu PK, Siegel NS. Sleep physiology, pathophysiology, and sleep hygiene. Prog Cardiovasc Dis. 2023;77:59–69.
35. Shen Y, et al. Circadian disruption and sleep disorders in neurodegeneration. Transl Neurodegener. 2023;12(1):8.
36. Calero K, W.M.J.J.o.C SM, Anderson. Can poor sleep cause kidney disease? Another step closer to the answer. J Clin Sleep Med. 2019;15(3):371–2.
37. Ali T, et al. Sleep, immunity and inflammation in gastrointestinal disorders. World J Gastroenterol. 2013;19(48):9231–9.
38. Ranjbaran Z, et al. Impact of sleep disturbances in inflammatory bowel disease. J Gastroenterol Hepatol. 2007;22(11):1748–53.
39. Chen MJ, et al. Gastroesophageal reflux disease and sleep quality in a chinese population. J Formos Med Assoc. 2009;108(1):53–60.
40. Ananthakrishnan AN, et al. Sleep disturbance and risk of active disease in patients with Crohn’s disease and ulcerative colitis. Clin Gastroenterol Hepatol. 2013;11(8):965–71.
41. Mazzon E, et al. Melatonin modulates signal transduction pathways and apoptosis in experimental colitis. J Pineal Res. 2006;41(4):363–73.
42. Necefli A, et al. The effect of melatonin on TNBS-induced colitis. Dig Dis Sci. 2006;51(9):1538–45.
43. Specian RD, Oliver MG. Functional biology of intestinal goblet cells. Am J Physiol. 1991;260(2 Pt 1):C183–93.
44. Stappenbeck TS. Paneth cell development, differentiation, and function: new molecular cues. Gastroenterology. 2009;137(1):30–3.
45. Poroyko VA, et al. Chronic sleep disruption alters gut microbiota, induces systemic and adipose tissue inflammation and insulin resistance in mice. Sci Rep. 2016;6(1):35405.
46. König J, et al. Human intestinal barrier function in health and disease. Clin Translational Gastroenterol. 2016;7(10):e196.
47. Irwin MR. Sleep and inflammation: partners in sickness and in health. Nat Rev Immunol. 2019;19(11):702–15.
48. Park YS, et al. Melatonin in the colon modulates intestinal microbiota in response to stress and sleep deprivation. Intest Res. 2020;18(3):325–36.
49. Lin PY. The study of intestinal epithelial monolayer development and its Interaction with Intestinal Subepithelial Myofibroblast. Los Angeles: University of California; 2019.
50. Yeung TM, et al. Regulation of self-renewal and differentiation by the intestinal stem cell niche. Cell Mol Life Sci. 2011;68(15):2513–23.
51. Powell AE, et al. The pan-ErbB negative regulator Lrig1 is an intestinal stem cell marker that functions as a tumor suppressor. Cell. 2012;149(1):146–58.
52. Peng L, et al. Effects of butyrate on intestinal barrier function in a Caco-2 cell monolayer model of intestinal barrier. Pediatr Res. 2007;61(1):37–41.
53. Kinnucan JA, et al. Sleep and inflammatory bowel disease: exploring the relationship between sleep disturbances and inflammation. Gastroenterol Hepatol. 2013;9(11):718.
54. Rutsch A, Kantsjö JB, Ronchi J. The gut-brain axis: how microbiota and host inflammasome influence brain physiology and pathology. Front Immunol. 2020;11:604179.
55. Wu H, et al. Enhanced oral bioavailability of puerarin using microemulsion vehicle. Drug Dev Ind Pharm. 2009;35(2):138–44.
56. Baranova IN, et al. Human SR-BI and SR-BII potentiate lipopolysaccharide-induced inflammation and acute liver and kidney injury in mice. J Immunol. 2016;196(7):3135–47.
57. Matute-Bello G, et al. An official american thoracic society workshop report: features and measurements of experimental acute lung injury in animals. Am J Respir Cell Mol Biol. 2011;44(5):725–38.
58. Ascon M, et al. Renal ischemia-reperfusion leads to long term infiltration of activated and effector-memory T lymphocytes. Kidney Int. 2009;75(5):526–35.
No related articles found!
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed