Comparative analysis of antidepressant-like effects of five herbal essential oils on mice with reserpine-induced depression

References

• Preljevic, V.T., Østhus, T.B.H., Os, I., Sandvik, L., Opjordsmoen, S., Nordhus, I.H., & Dammen, T. (2013). Anxiety and depressive disorders in dialysis patients: association to health-related quality of life and mortality. General Hospital Psychiatry. 35(6): 619-624. doi: 10.1016/j.genhosppsych.2013.05.006
   PubMed Web of Science ®Google Scholar
• Rahman, M.M., Islam, F., Parvez, A., Azad, M.A.K., Ashraf, G.M., Ullah, M.F., & Ahmed, M. (2022). Citrus limon L. (lemon) seed extract shows neuro-modulatory activity in an in vivo thiopental-sodium sleep model by reducing the sleep onset and enhancing the sleep duration. Journal of Integrative Neuroscience,.21(1). doi: 10.31083/j.jin2101042
   PubMed Web of Science ®Google Scholar
• Islam, F., Mitra, S., Nafady, M.H., Rahman, M.T., Tirth, V., Akter, A., Emran, T.B., Mohamed, A.A.R., Algahtani, A. and El-Kholy, S.S. (2022). Neuropharmacological and antidiabetic potential of Lannea coromandelica (houtt.) merr. Leaves extract: an experimental analysis. Evidence-Based Complementary and Alternative Medicine. 2022.
   Web of Science ®Google Scholar
• Duevel, J.A., Hasemann, L., Peña-Longobardo, L.M., Rodríguez-Sánchez, B., Aranda-Reneo, I., Oliva-Moreno, J., López-Bastida, J. and Greiner, W. 2020. (2020). Considering the societal perspective in economic evaluations: a systematic review in the case of depression. Health Economics Review. 10(1): 32. doi: 10.1186/s13561-020-00288-7
   PubMed Web of Science ®Google Scholar
• Akter, A., Islam, F., Bepary, S., Al-Amin, M., Begh, M.Z.A., Islam, M.A.F.U., Ashraf, G.M., Baeesa, S.S. and Ullah, M.F. (2022). CNS depressant activities of Averrhoa carambola leaves extract in thiopental-sodium model of Swiss albino mice: implication for neuro-modulatory properties. Biologia. 77(5): 1337-1346. doi: 10.1007/s11756-022-01057-z
   Web of Science ®Google Scholar
• Shenal, B.V., Harrison, D.W., & Demaree, H.A. (2003). The neuropsychology of depression: A literature review and preliminary model. Neuropsychology Review. 13(1): 33-42. doi: 10.1023/A:1022300622902
   PubMed Web of Science ®Google Scholar
• Kennedy, S.H., Andersen, H.F., & Thase, M.E. (2009). Escitalopram in the treatment of major depressive disorder: A meta-analysis. Current Medical Research and Opinion. 25(1): 161-175. doi: 10.1185/03007990802622726
   PubMed Web of Science ®Google Scholar
• Sánchez-Vidaña, D.I., Ngai, S.P.-C., He, W., Chow, J.K.-W., Lau, B.W.-M., & Tsang, H.W.-H. (2017). The effectiveness of aromatherapy for depressive symptoms: A systematic review. Evidence-Based Complementary and Alternative Medicine. 2017.
   Web of Science ®Google Scholar
• Xu, A., Chen, X., Jiang, J., Chen, Z., & Ding, P. (2016). Chemical constituents from Jasminum elongatum. Zhong yao cai= Zhongyaocai= Journal of Chinese Medicinal Materials. 39(8): 1779-1781.
   PubMedGoogle Scholar
• Rahman, M.M., Dhar, P.S., Anika, F., Ahmed, L., Islam, M.R., Sultana, N.A., Cavalu, S., Pop, O. and Rauf, A. (2022). Exploring the plant-derived bioactive substances as antidiabetic agent: An extensive review. Biomedicine & pharmacotherapy. 152: 113217-113217. doi: 10.1016/j.biopha.2022.113217
   PubMed Web of Science ®Google Scholar
• Islam, F., Khadija, J.F., Harun-Or-Rashid, M., Rahaman, M.S., Nafady, M.H., Islam, M.R., Akter, A., Emran, T.B., Wilairatana, P. and Mubarak, M.S. (2022). Bioactive Compounds and Their Derivatives: An Insight into Prospective Phytotherapeutic Approach against Alzheimer’s Disease. Oxidative Medicine and Cellular Longevity. 2022.
   Web of Science ®Google Scholar
• Mitra, S., Lami, M.S., Uddin, T.M., Das, R., Islam, F., Anjum, J., Hossain, M.J. and Emran, T.B. (2022). Prospective multifunctional roles and pharmacological potential of dietary flavonoid narirutin. Biomedicine & Pharmacotherapy. 150.
   Web of Science ®Google Scholar
• Rahman, M.M., Islam, M.R., Shohag, S., Hossain, M.E., Rahaman, M.S., Islam, F., Ahmed, M., Mitra, S., Khandaker, M.U., Idris, A.M. and Chidambaram, K. (2022). The Multifunctional Role of Herbal Products in the Management of Diabetes and Obesity: A Comprehensive Review. Molecules. 27(5).
   Web of Science ®Google Scholar
• Rahman, M.M., Bibi, S., Rahaman, M.S., Rahman, F., Islam, F., Khan, M.S., Hasan, M.M., Parvez, A., Hossain, M.A., Maeesa, S.K. and Islam, M.R. (2022). Natural therapeutics and nutraceuticalsfor lung diseases: Traditional significance, phytochemistry, and pharmacology. Biomedicine & pharmacotherapy. 150: 113041-113041. doi: 10.1016/j.biopha.2022.113041
   PubMed Web of Science ®Google Scholar
• Farag, M.A., & Al-Mahdy, D.A. (2013). Comparative study of the chemical composition and biological activities of Magnolia grandiflora and Magnolia virginiana flower essential oils. Natural Product Research. 27(12): 1091-1097. doi: 10.1080/14786419.2012.696256
   PubMed Web of Science ®Google Scholar
• Hyeon, H., Hyun, H.B., Go, B., Kim, S.C., Jung, Y.-H., & Ham, Y.-M. (2022). Profiles of essential oils and correlations with phenolic acids and primary metabolites in flower buds of Magnolia heptapeta and Magnolia denudata var. purpurascens. Molecules. 27(1).
   Web of Science ®Google Scholar
• Shi, S., Yan, H., Chen, Y., Liu, Y., Zhang, X., Xie, Y., Xu, J., Wu, L., Chen, K., Shen, X. and Ren, P. (2020). Pharmacokinetic study of precisely representative antidepressant, prokinetic, anti-inflammatory and anti-oxidative compounds from Fructus aurantii and Magnolia Bark. Chemico-Biological Interactions. 315: 108851. doi: 10.1016/j.cbi.2019.108851
   PubMed Web of Science ®Google Scholar
• Boskabady, M.H., Shafei, M.N., Saberi, Z., & Amini, S. (2011). Pharmacological effects of Rosa damascena. Iranian Journal of Basic Medical Sciences. 14(4): 295.
   PubMed Web of Science ®Google Scholar
• Nayebi, N., Khalili, N., Kamalinejad, M., & Emtiazy, M. (2017). A systematic review of the efficacy and safety of Rosa damascena Mill. with an overview on its phytopharmacological properties. Complementary Therapies in Medicine. 34: 129-140. doi: 10.1016/j.ctim.2017.08.014
   PubMed Web of Science ®Google Scholar
• Oukerrou, M.A., Tilaoui, M., Mouse, H.A., Leouifoudi, I., Jaafari, A., & Zyad, A. (2017). Chemical composition and cytotoxic and antibacterial activities of the essential oil of Aloysia citriodora palau grown in Morocco. Advances in Pharmacological Sciences. 2017. doi: 10.1155/2017/7801924
   PubMedGoogle Scholar
• Singh, R., Nath, G., Goel, R., & Bhattacharya, S. (1998). Pharmacological actions of Abies pindrow Royle leaf. Indian Journal of Experimental Biology. 36(2): 187-191.
   PubMedGoogle Scholar
• Tang, M., Ai, Y., Zhu, S., Song, N., Xu, X., Liang, L., Rong, B., Zheng, X., Zhang, L. and He, T. (2021). Antidepressant-like effect of essential oils from Citrus reticulata in reserpine-induced depressive mouse. Natural Product Communications. 17(5).
   Web of Science ®Google Scholar
• Liu, J., Garza, J.C., Bronner, J., Kim, C.S., Zhang, W., & Lu, X.-Y. (2010). Acute administration of leptin produces anxiolytic-like effects: a comparison with fluoxetine. Psychopharmacology. 207(4): 535-545. doi: 10.1007/s00213-009-1684-3
   PubMed Web of Science ®Google Scholar
• Zhang, B., Wang, P.P., Hu, K.L., Li, L.N., Yu, X., Lu, Y., & Chang, H.S. (2019). Antidepressant-like effect and mechanism of action of honokiol on the mouse lipopolysaccharide (LPS) depression model. Molecules. 24(11).
   Web of Science ®Google Scholar
• Jiang, X., Yi, S., Liu, Q., Su, D., Li, L., Xiao, C., & Zhang, J. (2022). Asperosaponin VI ameliorates the CMS-induced depressive-like behaviors by inducing a neuroprotective microglial phenotype in hippocampus via PPAR-γ pathway. J. Neuroinflammation. 19(1): 115. doi: 10.1186/s12974-022-02478-y
   PubMed Web of Science ®Google Scholar
• Cryan, J.F., Mombereau, C., & Vassout, A. (2005). The tail suspension test as a model for assessing antidepressant activity: review of pharmacological and genetic studies in mice. Neurosci. Biobehav. Rev. 29(4-5): 571-625. doi: 10.1016/j.neubiorev.2005.03.009
   PubMed Web of Science ®Google Scholar
• Abbasi-Maleki, S., Kadkhoda, Z., & Taghizad-Farid, R. (2020). The antidepressant-like effects of Origanum majorana essential oil on mice through monoaminergic modulation using the forced swimming test. Journal of Traditional and Complementary Medicine. 10(4): 327-335. doi: 10.1016/j.jtcme.2019.01.003
   PubMedGoogle Scholar
• Monteiro, Á.B., de Souza Rodrigues, C.K., do Nascimento, E.P., dos Santos Sales, V., de Araújo Delmondes, G., da Costa, M.H.N., de Oliveira, V.A.P., de Morais, L.P., Boligon, A.A., Barbosa, R. and da Costa, J.G.M. (2020). Anxiolytic and antidepressant-like effects of Annona coriacea (Mart.) and caffeic acid in mice. Food and Chemical Toxicology. 136: 111049. doi: 10.1016/j.fct.2019.111049
   PubMed Web of Science ®Google Scholar
• Tian, D.D., Wang, M., Liu, A., Gao, M.R., Qiu, C., Yu, W., Wang, W.J., Zhang, K., Yang, L., Jia, Y.Y. and Yang, C.B. (2021). Antidepressant effect of paeoniflorin is through inhibiting pyroptosis CASP-11/GSDMD pathway. Molecular Neurobiology. 58(2): 761-776. doi: 10.1007/s12035-020-02144-5
   PubMed Web of Science ®Google Scholar
• Wang, G., Lei, C., Tian, Y., Wang, Y., Zhang, L., & Zhang, R. (2019). Rb1, the primary active ingredient in Panax ginseng CA Meyer, exerts antidepressant-like effects via the BDNF–TrkB–CREB pathway. Frontiers in Pharmacology. 1034.
   Google Scholar
• Park, B.K., Kim, N.S., Kim, Y.R., Seo, C.S. and Lee, M.Y. (2020). Antidepressant and anti-neuroinflammatory effects of Bangpungtongsung-San. Frontiers in pharmacology, 958.
   Google Scholar
• Li, G., Yang, J., Wang, X., Zhou, C., Zheng, X., & Lin, W. (2020). Effects of EGCG on depression-related behavior and serotonin concentration in a rat model of chronic unpredictable mild stress. Food & Function. 11(10): 8780-8787. doi: 10.1039/D0FO00524J
   PubMed Web of Science ®Google Scholar
• Wang, Y., Wang, Y., Sun, R., Wu, X., Chu, X., Zhou, S., Hu, X., Gao, L. and Kong, Q. (2018). The treatment value of IL-1β monoclonal antibody under the targeting location of alpha-methyl-L-tryptophan and superparamagnetic iron oxide nanoparticles in an acute temporal lobe epilepsy model. Journal of Translational Medicine. 16(1): 1-13. doi: 10.1186/s12967-017-1374-6
   PubMedGoogle Scholar
• García-García, L., Shiha, A.A., de la Rosa, R.F., Delgado, M., Silván, Á., Bascuñana, P., Bankstahl, J.P., Gomez, F. and Pozo, M.A. (2017). Metyrapone prevents brain damage induced by status epilepticus in the rat lithium-pilocarpine model. Neuropharmacology. 123: 261-273. doi: 10.1016/j.neuropharm.2017.05.007
   PubMed Web of Science ®Google Scholar
• Luo, Y., Xiao, Q., Wang, J., Jiang, L., Hu, M., Jiang, Y., Tang, J., Liang, X., Qi, Y., Dou, X. and Zhang, Y. (2019). Running exercise protects oligodendrocytes in the medial prefrontal cortex in chronic unpredictable stress rat model. Translational psychiatry. 9(1): 1-11. doi: 10.1038/s41398-019-0662-8
   PubMedGoogle Scholar
• Ramírez-Rodríguez, G.B., Palacios-Cabriales, D.M., Ortiz-López, L., Estrada-Camarena, E.M., & Vega-Rivera, N.M. (2020). Melatonin modulates dendrite maturation and complexity in the dorsal-and ventral-dentate gyrus concomitantly with its antidepressant-like effect in male balb/c mice. International Journal of Molecular Sciences. 21(5): 1724. doi: 10.3390/ijms21051724
   PubMed Web of Science ®Google Scholar
• Odaira, T., Nakagawasai, O., Takahashi, K., Nemoto, W., Sakuma, W., Lin, J.-R., & Tan-No, K. (2019). Mechanisms underpinning AMP-activated protein kinase-related effects on behavior and hippocampal neurogenesis in an animal model of depression. Neuropharmacology. 150: 121-133. doi: 10.1016/j.neuropharm.2019.03.026
   PubMed Web of Science ®Google Scholar
• Chen, S., Guo, W., Qi, X., Zhou, J., Liu, Z., & Cheng, Y. (2019). Natural alkaloids from lotus plumule ameliorate lipopolysaccharide-induced depression-like behavior: integrating network pharmacology and molecular mechanism evaluation. Food & Function. 10(9): 6062-6073. doi: 10.1039/C9FO01092K
   PubMed Web of Science ®Google Scholar
• Zhang, J.J., Gao, T.T., Wang, Y., Wang, J.L., Guan, W., Wang, Y.J., Wang, C.N., Liu, J.F. and Jiang, B. (2019). Andrographolide exerts significant antidepressant-like effects involving the hippocampal BDNF system in mice. International Journal of Neuro-psychopharmacology. 22(9): 585-600.
   PubMed Web of Science ®Google Scholar
• Zhang, X., Yin, Y., Yue, L., & Gong, L. (2019). Selective serotonin reuptake inhibitors aggravate depression-associated dry eye via activating the NF-κB pathway. Investigative Ophthalmology & Visual Science. 60(1): 407-419. doi: 10.1167/iovs.18-25572
   PubMed Web of Science ®Google Scholar
• Sun, L., Verkaik-Schakel, R.-N., Biber, K., Plösch, T., & Serchov, T. (2021). Antidepressant treatment is associated with epigenetic alterations of Homer1 promoter in a mouse model of chronic depression. Journal of Affective Disorders. 279: 501-509. doi: 10.1016/j.jad.2020.10.040
   PubMed Web of Science ®Google Scholar
• Mitra, S., Anjum, J., Muni, M., Das, R., Rauf, A., Islam, F., Emran, T.B., Semwal, P., Hemeg, H.A., Alhumaydhi, F.A. and Wilairatana, P. (2022). Exploring the journey of emodin as a potential neuroprotective agent: Novel therapeutic insights with molecular mechanism of action. Biomedicine & Pharmacotherapy. 149. doi: 10.1016/j.biopha.2022.112877
   PubMed Web of Science ®Google Scholar
• Cherian, K., Schatzberg, A.F., & Keller, J. (2019). HPA axis in psychotic major depression and schizophrenia spectrum disorders: Cortisol, clinical symptomatology, and cognition. Schizophrenia Research. 213: 72-79. doi: 10.1016/j.schres.2019.07.003
   PubMed Web of Science ®Google Scholar
• Zunszain, P.A., Anacker, C., Cattaneo, A., Carvalho, L.A., & Pariante, C.M. (2011). Glucocorticoids, cytokines and brain abnormalities in depression. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 35(3): 722-729. doi: 10.1016/j.pnpbp.2010.04.011
   PubMed Web of Science ®Google Scholar
• Tripathi, S.J., Chakraborty, S., Srikumar, B.N., Raju, T.R., & Rao, B.S.S. (2019). Prevention of chronic immobilization stress-induced enhanced expression of glucocorticoid receptors in the prefrontal cortex by inactivation of basolateral amygdala. Journal of Chemical Neuroanatomy. 95: 134-145. doi: 10.1016/j.jchemneu.2017.12.006
   PubMed Web of Science ®Google Scholar
• Duman, R.S., Malberg, J., & Thome, J. (1999). Neural plasticity to stress and antidepressant treatment. Biological Psychiatry. 46(9): 1181-1191. doi: 10.1016/S0006-3223(99)00177-8
   PubMed Web of Science ®Google Scholar
• Pilar-Cuéllar, F., Vidal, R., Díaz, A., Castro, E., dos Anjos, S., Pascual-Brazo, J., Linge, R., Vargas, V., Blanco, H., Martínez-Villayandre, B. and Pazos, Á. (2013). Neural plasticity and proliferation in the generation of antidepressant effects: hippocampal implication. Neural Plasticity. 2013. doi: 10.1155/2013/537265
   PubMed Web of Science ®Google Scholar
• Nordanskog, P., Larsson, M.R., Larsson, E. M., & Johanson, A. (2014). Hippocampal volume in relation to clinical and cognitive outcome after electroconvulsive therapy in depression. Acta Psychiatrica Scandinavica. 129(4): 303-311. doi: 10.1111/acps.12150
   PubMed Web of Science ®Google Scholar
• Wiley, J.W., Higgins, G.A., & Athey, B.D. (2016). Stress and glucocorticoid receptor transcriptional programming in time and space: Implications for the brain-gut axis. Neurogastroenterology and Motility. 28(1): 12-25. doi: 10.1111/nmo.12706
   PubMed Web of Science ®Google Scholar
• Christmas, D.M., Potokar, J.P., & Davies, S.J.C. (2011). A biological pathway linking inflammation and depression: activation of indoleamine 2,3-dioxygenase. Neuropsychiatric Disease and Treatment. 7: 431-439.
   PubMed Web of Science ®Google Scholar
• Troubat, R., Barone, P., Leman, S., Desmidt, T., Cressant, A., Atanasova, B., Brizard, B., El Hage, W., Surget, A., Belzung, C. and Camus, V. (2021). Neuroinflammation and depression: A review. European Journal of Neuroscience, 53(1): 151-171. doi: 10.1111/ejn.14720
   PubMed Web of Science ®Google Scholar