Pharmacopsychiatry 2021; 54(05): 215-223
DOI: 10.1055/a-1349-3870
Original Paper

Withanone Ameliorates Stress Symptoms in Caenorhabditis Elegans by Acting through Serotonin Receptors

Janine Naß
Department of Pharmaceutical Biology, Institute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany
,
Thomas Efferth
Department of Pharmaceutical Biology, Institute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany
› Institutsangaben

ABSTRACT

Introduction Depression is responsible for 800 000 deaths worldwide, a number that will rise significantly due to the COVID-19 pandemic. Affordable novel drugs with less severe side effects are urgently required. We investigated the effect of withanone (WN) from Withania somnifera on the serotonin system of wild-type and knockout Caenorhabditis elegans strains using in silico, in vitro, and in vivo methods.

Methods WN or fluoxetine (as positive control drug) was administered to wild-type (N2) and knockout C. elegans strains (AQ866, DA1814, DA2100, DA2109, and MT9772) to determine their effect on oxidative stress (Trolox, H2DCFDA, and juglone assays) on osmotic stress and heat stress and lifespan. Quantitative real-time RT-PCR was applied to investigate the effect of WN or fluoxetine on the expression of serotonin receptors (ser-1, ser-4, ser-7) and serotonin transporter (mod-5). The binding affinity of WN to serotonin receptors and transporter was analyzed in silico using AutoDock 4.2.6.

Results WN scavenged ROS in wild-type and knockout C. elegans and prolonged their lifespan. WN upregulated the expression of serotonin receptor and transporter genes. In silico analyses revealed high binding affinities of WN to Ser-1, Ser-4, Ser-7, and Mod-5.

Limitations Further studies are needed to prove whether the results from C. elegans are transferrable to mammals and human beings.

Conclusion WN ameliorated depressive-associated stress symptoms by activating the serotonin system. WN may serve as potential candidate in developing new drugs to treat depression.

Supplementary Material



Publikationsverlauf

Artikel online veröffentlicht:
06. Mai 2021

© 2021. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 World Health Organization. Depression and other common mental disorders: Global health estimates; 2017; https://apps.who.int/iris/handle/10665/254610 Accessed on February 19, 2021
  • 2 Kanter JMK. COVID-19 could lead to an epidemic of clinical depression, and the health care system isn’t ready for that, either. 2020; https://theconversation.com/covid-19-could-lead-to-an-epidemic-of-clinical-depression-and-the-health-care-system-isnt-ready-for-that-either-134528. Accessed on February 19, 2021
  • 3 Zhang Y, Chen Y, Ma L. Depression and cardiovascular disease in elderly: Current understanding. J Clin Neurosci 2018; 47: 1-5
  • 4 Rivera M, Porras-Segovia A, Rovira P. et al. Associations of major depressive disorder with chronic physical conditions, obesity and medication use: Results from the PISMA-ep study. Eur Psychiatry 2019; 60: 20-27
  • 5 Crawford AA, Lewis S, Nutt D. et al. Adverse effects from antidepressant treatment: randomised controlled trial of 601 depressed individuals. Psychopharmacology (Berl) 2014; 231: 2921-2931
  • 6 Bellivier F, Henry C, Szöke A. et al. Serotonin transporter gene polymorphisms in patients with unipolar or bipolar depression. Neurosci Lett 1998; 255: 143-146
  • 7 Yuan H, Zhu X, Luo Q. et al. Early symptom non-improvement and aggravation are associated with the treatment response to SSRIs in MDD: a real-world study. Neuropsychiatr Dis Treat 2019; 15: 957-966
  • 8 Li J, OW Li W. et al. Oxidative stress and neurodegenerative disorders. Int J Mol Sci 2013; 14: 24438-24475
  • 9 Angelova PR, Abramov AY. Role of mitochondrial ROS in the brain: From physiology to neurodegeneration. FEBS Lett 2018; 592: 692-702
  • 10 Wadhwa R, Gupta R, Maurya PK. Oxidative stress and accelerated aging in neurodegenerative and neuropsychiatric disorder. Curr Pharm Des 2018; 24: 4711-4725
  • 11 Chung CP, Schmidt D, Stein CM. et al. Increased oxidative stress in patients with depression and its relationship to treatment. Psychiatry Res 2013; 206: 213-216
  • 12 Maes M, Kubera M, Mihaylova I. et al. Increased autoimmune responses against auto-epitopes modified by oxidative and nitrosative damage in depression: implications for the pathways to chronic depression and neuroprogression. J Affect Disord 2013; 149: 23-29
  • 13 Sperner-Unterweger B, Kohl C, Fuchs D. Immune changes and neurotransmitters: Possible interactions in depression?. Prog Neuropsychopharmacol Biol Psychiatry 2014; 48: 268-276
  • 14 Krishnan V, Nestler EJ. The molecular neurobiology of depression. Nature 2008; 455: 894-902
  • 15 Liu L, Liu C, Wang Y. et al. Herbal medicine for anxiety, depression and insomnia. Curr Neuropharmacol 2015; 13: 481-493
  • 16 Wang Y, Li M, Liang Y. et al. Chinese herbal medicine for the treatment of depression: Applications, efficacies and mechanisms. Curr Pharm Des 2017; 23: 5180-5190
  • 17 Sarris J, Panossian A, Schweitzer I. et al. Herbal medicine for depression, anxiety and insomnia: a review of psychopharmacology and clinical evidence. Eur Neuropsychopharmacol 2011; 21: 841-860
  • 18 Ren Y, Zhu C, Wu J. et al. Comparison between herbal medicine and fluoxetine for depression: a systematic review of randomized controlled trials. Complement Ther Med 2015; 23: 674-684
  • 19 Ismail H, Amanat MA, Iqbal A. et al. Medicinal plants: A complementary and alternative antidepressant therapy. Curr Pharm Des 2018; 24: 2609-2624
  • 20 Singh N, Bhalla M, Jager Pde. et al. An overview on ashwagandha: a Rasayana (rejuvenator) of Ayurveda. Afr J Tradit Complement Altern Med 2011; 8: 208-213
  • 21 Konar A, Shah N, Singh R. et al. Protective role of Ashwagandha leaf extract and its component withanone on scopolamine-induced changes in the brain and brain-derived cells. PLoS One 2011; 6: e27265
  • 22 Panossian A, Seo EJ, Efferth T. Effects of anti-inflammatory and adaptogenic herbal extracts on gene expression of eicosanoids signaling pathways in isolated brain cells. Phytomedicine 2019; 60: 152881
  • 23 Garg S, Kaul SC, Wadhwa R. Anti-stress and glial differentiation effects of a novel combination of cucurbitacin B and withanone (CucWi-N): Experimental evidence. Ann Neurosci 2018; 25: 201-209
  • 24 Kaletta T, Hengartner MO. Finding function in novel targets: C. elegans as a model organism. Nat Rev Drug Discov 2006; 5: 387-398
  • 25 Rodriguez M, Snoek LB, Bono Mde. et al. Worms under stress: C. elegans stress response and its relevance to complex human disease and aging. Trends Genet 2013; 29: 367-374
  • 26 Ding X, Njus Z, Kong T. et al. Effective drug combination for Caenorhabditis elegans nematodes discovered by output-driven feedback system control technique. Sci Adv 2017; 3: eaao1254
  • 27 O’Reilly LP, Luke CJ, Perlmutter DH. et al. C. elegans in high-throughput drug discovery. Adv Drug Deliv Rev 2014; 69-70: 247-453
  • 28 Ni YG, Miledi R. Blockage of 5HT2C serotonin receptors by fluoxetine (Prozac). Proc Natl Acad Sci USA 1997; 94: 2036-2040
  • 29 Zafir A, Banu N. Antioxidant potential of fluoxetine in comparison to Curcuma longa in restraint-stressed rats. Eur J Pharmacol 2007; 572: 23-31
  • 30 Girard LR, Fiedler TJ, Harris TW. et al. WormBook: The online review of Caenorhabditis elegans biology. Nucleic Acids Res 2007; 35: D472-D475
  • 31 Strange K. An overview of C. elegans biology. Methods Mol Biol 2006; 351: 1-11
  • 32 Wongchai K, Schlotterer A, Lin J. et al. Protective effects of liraglutide and linagliptin in C. elegans as a new model for glucose-induced neurodegeneration. Horm Metab Res 2016; 48: 70-75
  • 33 Miller NJ, Rice-Evans C, Davies MJ. et al. A novel method for measuring antioxidant capacity and its application to monitoring the antioxidant status in premature neonates. Clin Sci 1993; 84: 407-412
  • 34 Naß J, Efferth T. Ursolic acid ameliorates stress and reactive oxygen species in C. elegans knockout mutants by the dopamine Dop1 and Dop3 receptors. Phytomedicine 2021; 81: 153439
  • 35 Naß J, Abdelfatah S, Efferth T. Ursolic acid enhances stress resistance, reduces ROS accumulation and prolongs life span in C. elegans serotonin-deficient mutants. Food Funct 2021; https://doi.org/10.1039/d0fo02208j; PMID: 33596295
  • 36 Naß J, Abdelfatah S, Efferth T. Induction of stress resistance and extension of lifespan in Chaenorhabditis elegans serotonin-receptor knockout strains by withanolide A. Phytomedicine. 2021; 84: 153482
  • 37 Solomon A, Bandhakavi S, Jabbar S. et al. Caenorhabditis elegans OSR-1 regulates behavioral and physiological responses to hyperosmotic environments. Genetics 2004; 167: 161-170
  • 38 Zevian SC, Yanowitz JL. Methodological considerations for heat shock of the nematode Caenorhabditis elegans. Methods 2014; 68: 450-457
  • 39 Sutphin GL, Kaeberlein M. Measuring Caenorhabditis elegans life span on solid media. J Vis Exp 2009; 27: 1152
  • 40 Zhang Y, Chen D, Smith MA. et al. Selection of reliable reference genes in Caenorhabditis elegans for analysis of nanotoxicity. PLoS One 2012; 7: e31849
  • 41 Kiefer F, Arnold K, Künzli M. et al. The SWISS-MODEL Repository and associated resources. Nucleic Acids Res 2009; 37: D387-D392
  • 42 Dallakyan S, Olson AJ. Small-molecule library screening by docking with PyRx. Methods Mol Biol 2015; 1263: 243-250
  • 43 Morris GM, Huey R, Lindstrom W. et al. AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility. J Comput Chem 2009; 30: 2785-2791
  • 44 Humphrey W, Dalke A, Schulten K. VMD: visual molecular dynamics. J Mol Graph 1996; 1: 33-38
  • 45 Kadioglu O, Saeed ME, Valoti M. et al. Interactions of human P-glycoprotein transport substrates and inhibitors at the drug binding domain: Functional and molecular docking analyses. Biochem Pharmacol 2016; 104: 42-51
  • 46 Han SK, Lee D, Lee H. et al. OASIS 2: online application for survival analysis 2 with features for the analysis of maximal lifespan and healthspan in aging research. Oncotarget 2016; 7: 56147-56152
  • 47 GraphPad Prism. La Jolla California USA 2020 Available from URL www.graphpad.com
  • 48 Huether G, Fettkötter I, Keilhoff G. et al. Serotonin acts as a radical scavenger and is oxidized to a dimer during the respiratory burst of activated microglia. J Neurochem 1997; 69: 2096-2101
  • 49 Lv J, Liu F. The role of serotonin beyond the central nervous system during embryogenesis. Front Cell Neurosci 2017; 11: 74
  • 50 Herr N, Bode C, Duerschmied D. The effects of serotonin in immune cells. Front Cardiovasc Med 2017; 4: 48i https://doi.org/10.3389/fcvm.2017.00048
  • 51 Dar NJ, Bhat JA, Satti NK. et al. Withanone, an active constituent from Withania somnifera, affords protection against NMDA-induced excitotoxicity in neuron-like cells. Mol Neurobiol 2017; 54: 5061-5073 https://doi.org/10.1007/s12035-016-0044-7; PMID: 27541286
  • 52 Bhattacharya SK, Satyan KS, Ghosal S. Antioxidant activity of glycowithanolides from Withania somnifera. Indian J Exp Biol 1997; 35: 236-239 PMID: 9332168
  • 53 Ahmad T, Suzuki YJ. Juglone in oxidative stress and cell signaling. Antioxidants (Basel) 2019; 8: 91
  • 54 Hukema RK, Rademakers S, Jansen G. Gustatory plasticity in C. elegans involves integration of negative cues and NaCl taste mediated by serotonin, dopamine, and glutamate. Learn Mem 2008; 15: 829-836
  • 55 Martinière A, Fiche JB, Smokvarska M. et al. Osmotic stress activates two reactive oxygen species pathways with distinct effects on protein nanodomains and diffusion. Plant Physiol 2019; 179: 1581-1593
  • 56 Tatum MC, Ooi FK, Chikka MR. et al. Neuronal serotonin release triggers the heat shock response in C. elegans in the absence of temperature increase. Curr Biol 2015; 25: 163-174
  • 57 Slimen IB, Najar T, Ghram A. et al. Reactive oxygen species, heat stress and oxidative-induced mitochondrial damage. A review. Int J Hyperthermia 2014; 30: 513-523
  • 58 Yu Y-B, Dosanjh L, Lao L. et al. Cinnamomum cassia bark in two herbal formulas increases life span in Caenorhabditis elegans via insulin signaling and stress response pathways. PLoS One 2010; 5: e9339
  • 59 Murakami H, Murakami S. Serotonin receptors antagonistically modulate Caenorhabditis elegans longevity. Aging Cell 2007; 6: 483-488
  • 60 Nikiforuk A. Targeting the Serotonin 5-HT7 Receptor in the search for treatments for CNS disorders: Rationale and progress to date. CNS Drugs 2015; 29: 265-275
  • 61 Petrascheck M, Ye X, Buck LB. An antidepressant that extends lifespan in adult Caenorhabditis elegans. Nature 2007; 450: 553-556
  • 62 Kumar R, Gupta K, Saharia K. et al. Withania somnifera root extract extends lifespan of Caenorhabditis elegans. Ann Neurosci 2013; 20: 13-16
  • 63 Larsen PL. Aging and resistance to oxidative damage in Caenorhabditis elegans. Proc Natl Acad Sci USA 1993; 90: 8905-8909
  • 64 Wang H, Liu J, Li T. et al. Blueberry extract promotes longevity and stress tolerance via DAF-16 in Caenorhabditis elegans. Food Funct 2018; 9: 5273-5282 https://doi.org/10.1039/c8fo01680a
  • 65 Wiegant FA, Surinova S, Ytsma E. et al. Plant adaptogens increase lifespan and stress resistance in C. elegans. Biogerontology 2009; 10: 27-42