D02. Linalool Exerted a Neuroprotective Activity against Corticosterone-induced Apoptosis of PC12 cells

Main Article Content

Somrudee Saiyudthong
Niphat Jirapongwattana
Yamaratee Jaisin
Punnee Nusuetrong

Abstract

Introduction: Linalool is an active compound found in many essential oils having sedative, anxiolytic and analgesic properties. Therefore, these essential oils have been usually used in aromatherapy to reduce stress. However, the mechanism underlying anti-stress of linalool has not been investigated.


Objective: To investigate the mechanism of neuroprotective action of linalool on corticosterone-induced neurotoxicity in PC12 cells.


Methods: PC12 cells were treated with 650 μM of corticosterone in the absence or presence of linalool or fluoxetine for 24 hours. PC12 was treated with corticosterone 650 μM and difference concentration of linalool (100, 200, 300, 400, 500, 600 and 700 μM) for 24 hours. Methyl thiazolyl tetrazolium (MTT) assay and lactate dehydrogenase (LDH) detection were investigated to confirm the neuroprotective effect of linalool against cell damage caused by corticosterone. Then, the intracellular Ca2+ content was measured by fluorescent labeling.


Results: Linalool 100 and 200 μM significantly increased cell viability compared with the group treated with corticosterone alone (p<0.05). Linalool 100, 200, 300 and 400 μM significantly (p<0.05) reduced LDH release. Linalool (100, 200, 300, 400, 500 and 600 μM) tend to revere the increased intracellular Ca2+produced by corticosterone.


Conclusion: These findings indicated that linalool exerted a neuroprotective activity against corticosterone-induced neuronal apoptosis in PC12 cells. The mechanism underlying this action may be partly due to the attenuation of intracellular Ca2+ overloading under stress conditions. However, further studies need to investigate the precise cellular and molecular mechanisms underlying this neuroprotective activity of linalool.

Article Details

How to Cite
Saiyudthong, S. ., Jirapongwattana, N. ., Jaisin, Y. ., & Nusuetrong, P. . (2022). D02. Linalool Exerted a Neuroprotective Activity against Corticosterone-induced Apoptosis of PC12 cells. Journal of Health Science and Alternative Medicine, 242–246. Retrieved from https://he01.tci-thaijo.org/index.php/jhealthscialternmed/article/view/257807
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Original Article

References

Kupferberg A, Bicks L, Hasler G. Social functioning in major depressive disorder. NeurosciBiobehav Rev. 2016; 69:313–32.2016.07.002

Friedrich MJ. Depression is the leading cause of disability around the world. JAMA. 2017; 317(15):1517.

Aihara M, Ida I, Yuuki N, Oshima A, Kumano H, Takahashi K, et al. HPA axis dysfunction in unmedicated major depressive disorder and its normalization by pharmacotherapy correlates with alteration of neural activity in prefrontal cortex and limbic/paralimbic regions. Psychiatry Res 2007; 155(3):245–56.

Varghese FP, Brown ES. The hypothalamic-pituitary-adrenal axis in major depressive disorder: A brief primer for primary care physicians. Prim Care Companion J Clin Psychiatry. 2001; 3(4):151–5.

Paslakis G, Heuser I, Schweiger U, Deuschle M. A single DEX/CRH test in male drug-free depressed patients is associated with the clinical response to treatment with fluoxetine. J Psychiatr Res. 2010; 44(16):1154–7.

Nahas R, Sheikh O. Complementary and alternative medicine for the treatment of major depressive disorder. Can Fam Physician. 2011; 57(6):659–63.

Cooke B, Ernst E. Aromatherapy: a systematic review. Br J Gen Pract. 2000; 50(455):493–6.

Kageyama A, Ueno T, Oshio M, Masuda H, Horiuchi H, Yokogoshi H. Antidepressant-like effects of an aqueous extract of lavender (Lavandulaangustifolia mill.) in rats. Food SciTechnol Res. 2012; 18(3):473–9.

Firoozeei TS, Feizi A, Rezaeizadeh H, Zargaran A, Roohafza HR, Karimi M. The antidepressant effects of lavender (Lavandulaangustifolia Mill.): A systematic review and meta-analysis of randomized controlled clinical trials. Complement Ther Med. 2021; 59(102679):102679.

Watanabe E, Kuchta K, Kimura M, Rauwald HW, Kamei T, Imanishi J. Effects of bergamot ( Citrus bergamia (Risso) Wright &Arn.) essential oil aromatherapy on mood states, parasympathetic nervous system activity, and salivary cortisol levels in 41 healthy females. ForschKomplementmed. 2015; 22(1):43–9.

Linck VM, da Silva AL, Figueiró M, Caramão EB, Moreno PRH, Elisabetsky E. Effects of inhaled Linalool in anxiety, social interaction and aggressive behavior in mice. Phytomedicine. 2010; 17(8–9):679–83.

Coelho V, Mazzardo-Martins L, Martins DF, Santos ARS, da Silva Brum LF, Picada JN, et al. Neurobehavioral and genotoxic evaluation of (-)-linalool in mice. J Nat Med. 2013; 67(4):876–80.

Alinejad B, Ghorbani A, Sadeghnia HR. Effects of combinations of curcumin, linalool, rutin, safranal, and thymoquinone on glucose/serum deprivation-induced cell death. Avicenna J Phytomed. 2013 Autumn; 3(4):321–8.

Migheli R, Lostia G, Galleri G, Rocchitta G, Serra PA, Bassareo V, et al. Neuroprotective effect of (R)-(-)-linalool on oxidative stress in PC12 cells. Phytomedicine Plus. 2021; 1(4):100073.

Ahmadi H , Morshedloo M R, Emrahi R , Javanmard A, Rasouli F, Maggi F, Kumar M, Manuel Lorenzo J. Introducing Three New Fruit-Scented Mints to Farmlands: Insights on Drug Yield, Essential-Oil Quality, and Antioxidant Properties. Antioxidants. 2022; 11: 866.

Simić A , Soković MD, Ristić M, Grujić-Jovanović S, Vukojević J, Marin PD. The chemical composition of some Lauraceae essential oils and their antifungal activities Phytother Res. 2004;18(9):713-7.

Kamatou GPP, Viljoen AM. Linalool – A Review of a Biologically Active Compound of Commercial Importance. Nat. Prod. Commun. 2008; 3 (7): 1883-1192

Deepa B, Venkatraman Anuradha C. Effects of linalool on inflammation, matrix accumulation and podocyte loss in kidney of streptozotocin-induced diabetic rats. Toxicol Mechan Methods. 2013; 23: 223–34.

Maeda H, Yamazaki M, Katagata Y. Kuromoji (Lindera umbellata) essential oil inhibits LPS-induced inflammation in RAW 264.7 cells. Biosci Biotechnol Biochem. 2013; 77: 482–6.

Li Y, Lv O, Zhou F, Li Q, Wu Z, Zheng Y. Linalool inhibits LPS-induced inflammation in BV2 microglia cells by activating Nrf2. Neurochem Res. 2015; 40: 1520–5.

López V, Nielsen B, Solas M, Ramírez MJ, Jäger AK. Exploring pharmacological mechanisms of lavender (Lavandula angustifolia) essential oil on central nervous system targets. Front Pharmacol. 2017; 8: 280.

Li Y-F, Luo Z-P. Desipramine antagonized corticosterone-induced apoptosis in cultured PC12 cells. ActaPharmacol Sin. 2002; 23(4):311–4.

Li YF, Gong ZH, Yang M, Zhao YM, Luo ZP. Inhibition of the oligosaccharides extracted from Morinda officinalis, a Chinese traditional herbal medicine, on the corticosterone induced apoptosis in PC12 cells. Life Sci. 2003; 72(8):933–42.

Wu Z, Wang G, Wang H, Xiao L, Wei Y, Yang C. Fluoxetine exposure for more than 2 days decreases the neuronal plasticity mediated by CRMP2 in differentiated PC12 cells. Brain Res Bull. 2020; 158:99–107.

Hwang S, Kim J-K. Fluoxetine induces apoptotic and oxidative neuronal death associated with the influx of copper ions in cultured neuronal cells. Chonnam Med J. 2020; 56(1):20–6.

Li Z-Y, Guo Z, Liu Y-M, Liu X-M, Chang Q, Liao Y-H, et al. Neuroprotective effects of total saikosaponins of Bupleurumyinchowense on corticosterone-induced apoptosis in PC12 cells. J Ethnopharmacol. 2013; 148(3):794–803.

Berridge MJ. Calcium signallingremodelling and disease. BiochemSoc Trans. 2012; 40(2):297–309.

Jiang BP, Liu YM, Le L, Li ZY, Si JY, Liu XM, Chang Q, Pan R. Cajaninstilbene Acid Prevents Corticosterone-Induced Apoptosis in PC12 Cells by Inhibiting the Mitochondrial Apoptotic Pathway. Cell PhysiolBiochem 2014;34:1015-102.