Comparative Study of Different Acorus Species in Potentiating Neuronal Differentiation in Cultured PC12 Cells
Kelly Y.C. Lam
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
Search for more papers by this authorYun Huang
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
Search for more papers by this authorPing Yao
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
Search for more papers by this authorHuaiyou Wang
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
HKUST Shenzhen Research Institute, Hi-Tech Park, Nanshan, Shenzhen, Guangdong Province, China
Search for more papers by this authorTina T.X. Dong
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
HKUST Shenzhen Research Institute, Hi-Tech Park, Nanshan, Shenzhen, Guangdong Province, China
Search for more papers by this authorZhongyu Zhou
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
Key Laboratory of Plant Resources Conservation and Sustainable Utilization, Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China
Search for more papers by this authorCorresponding Author
Karl W.K. Tsim
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
HKUST Shenzhen Research Institute, Hi-Tech Park, Nanshan, Shenzhen, Guangdong Province, China
Correspondence to: Professor Karl W.K. Tsim, Division of Life Science, Center for Chinese Medicine The Hong Kong University of Science and Technology, Clear Water Bay Road, Hong Kong SAR, China.
E-mail: [email protected]
Search for more papers by this authorKelly Y.C. Lam
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
Search for more papers by this authorYun Huang
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
Search for more papers by this authorPing Yao
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
Search for more papers by this authorHuaiyou Wang
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
HKUST Shenzhen Research Institute, Hi-Tech Park, Nanshan, Shenzhen, Guangdong Province, China
Search for more papers by this authorTina T.X. Dong
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
HKUST Shenzhen Research Institute, Hi-Tech Park, Nanshan, Shenzhen, Guangdong Province, China
Search for more papers by this authorZhongyu Zhou
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
Key Laboratory of Plant Resources Conservation and Sustainable Utilization, Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China
Search for more papers by this authorCorresponding Author
Karl W.K. Tsim
Division of Life Science, Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
HKUST Shenzhen Research Institute, Hi-Tech Park, Nanshan, Shenzhen, Guangdong Province, China
Correspondence to: Professor Karl W.K. Tsim, Division of Life Science, Center for Chinese Medicine The Hong Kong University of Science and Technology, Clear Water Bay Road, Hong Kong SAR, China.
E-mail: [email protected]
Search for more papers by this authorAbstract
Acori Tatarinowii Rhizoma (ATR), the rhizome of Acorus tatarinowii Schott, is a common traditional Chinese medicine being used clinically for mental disorder. However, other Acorus species herbs are all having the same Chinese name ‘Chang Pu’, making the confusion in herbal market. Acori Graminei Rhizoma (AGR) and Acori Calami Rhizoma (ACR) are common adulterants of ATR. Here, we aim to provide a comparative analysis between ATR, AGR, and ACR in potentiating neuronal differentiation. Volatile oil, derived from Acorus species, was applied onto cultured PC12 cells, and various parameters were determined: (i) transcriptional activation of neurofilament promoters was determined by the promoter-driven luciferase activity assay; (ii) the neurite outgrowth of PC12 cells was captured and measured; and (iii) the neurofilament expression and its underlying mechanism were analyzed by western blotting. The co-treatment of ATR, AGR, or ACR volatile oil with low concentration of nerve growth factor (NGF) could potentiate the NGF-induced neuronal differentiation in cultured PC12 cells. In addition, application of protein kinase A inhibitor H89 in cultures blocked the induction of neurofilament. Among these three Acorus species, ATR volatile oil showed the highest NGF-induced induction in neurite outgrowth and neurofilament expression, as compared with that of AGR and ACR. Copyright © 2017 John Wiley & Sons, Ltd.
Supporting Information
Filename | Description |
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ptr5904-supp-0001Fig_S1.tifTIFF image, 8.4 MB |
Fig. S1 Effect of Acori Tatarinowii Rhizoma, Acori Graminei Rhizoma, or Acori Calami Rhizoma volatile oil on the viability of PC12 cells. Cultured PC12 cells were treated with the different doses (0.3 to 300 μg/mL) of Acori Tatarinowii Rhizoma, Acori Graminei Rhizoma, or Acori Calami Rhizoma volatile oil for 48 h. Cell viability (using the colorimetric MTT assay) was performed. No significant increase in cell viability was observed. Values were expressed in percentage of control in cell number and in mean ± SEM, n = 5, each with triplicate samples. |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
References
- Bang JH, Lee KM, Lee IS, Heo EJ, Kang HW, Jeon WK. 2013. Evaluation of the effects of Acorus gramineus and Acorus tatarinowii extracts on a rat model of arterial thrombosis induced by ferric chloride. Natural Product Sciences 19: 251–257.
- Chen JP, Maiwulanjiang M, Lam KY, et al. 2014. A standardized extract of the fruit of Ziziphus jujuba (Jujube) induces neuronal differentiation of cultured PC12 cells: a signaling mediated by protein kinase A. J Agric Food Chem 62: 1890–1897.
- Choi GY, Ko BS, Lee MY, et al. 2011. Comparative study of changpo species on antioxidant activity and HPLC pattern analysis. Korean J Herbology 26: 13–19.
- Delghandi MP, Johannessen M, Moens U. 2005. The cAMP signalling pathway activates CREB through PKA, p38 and MSK1 in NIH 3T3 cells. Cell Signal 17: 1343–1351.
- Feng XL, Yu Y, Qin DP, Gao H, Yao XS. 2015. Acorus Linnaeus: a review of traditional uses, phytochemistry and neuropharmacology. RSC Adv 5: 5173–5182.
- Han P, Han T, Peng W, Wang XR. 2013. Antidepressant-like effects of essential oil and asarone, a major essential oil component from the rhizome of Acorus tatarinowii. Pharm Biol 51: 589–594.
- Hou Y, Wang Y, Zhao J, et al. 2014. Smart soup, a traditional Chinese medicine formula, ameliorates amyloid pathology and related cognitive deficits. PLoS One 9: e111215.
- Jagasia R, Steib K, Englberger E, et al. 2009. GABA-cAMP response element-binding protein signaling regulates maturation and survival of newly generated neurons in the adult hippocampus. J Neurosci 29: 7966–7977.
- Jaiswal Y, Liang Z, Ho A, Chen H, Zhao Z. 2015. Metabolite profiling of tissues of Acorus calamus and Acorus tatarinowii rhizomes by using LMD, UHPLC-QTOF MS, and GC-MS. Planta Med 81: 333–341.
- Jo JE, Lee AY, Kim HS, et al. 2013. Classification and comparative analysis of the contents of Acorus species and Anemone altaica by UPLC-PDA analysis. Korean J Food Sci Technol 45: 279–284.
10.9721/KJFST.2013.45.3.279 Google Scholar
- Kim KH, Kang HR, Eom HJ, Kim CS, Choi SU, Lee KR. 2015. A new aliphatic alcohol and cytotoxic chemical constituents from Acorus gramineus rhizomes. Biosci Biotechnol Biochem 79: 1402–1405.
- Lam KY, Ku CF, Wang HY, et al. 2016a. Authentication of Acori Tatarinowii Rhizoma (Shi Chang Pu) and its adulterants by morphological distinction, chemical composition and ITS sequencing. Chinas Med 11: 41.
- Lam CT, Gong AG, Lam KY, et al. 2016b. Jujube-containing herbal decoctions induce neuronal differentiation and the expression of anti-oxidant enzymes in cultured PC12 cells. J Ethnopharmacol 188: 275–283.
- Lam KY, Chen JP, Lam CT, et al. 2016c. Asarone from Acori Tatarinowii Rhizoma potentiates the nerve growth factor-induced neuronal differentiation in cultured PC12 cells: a signaling mediated by protein kinase A. PLoS One 11: e0163337.
- Lee JY, Yu SM, Sim HJ, Ko SK, Jong J. 2013. Comparative profiling of volatile composition from different Acorus species by solid-phase microextraction-gas chromatography/mass spectrometry. Anal Methods 5: 3675–3687.
- Lee B, Sur B, Yeom M, Shim I, Lee H, Hahm DH. 2014. Alpha-asarone, a major component of Acorus gramineus, attenuates corticosterone-induced anxiety-like behaviours via modulating TrkB signaling process. Korean J Physiol Pharmacol 18: 191–200.
- Liu ZB, Niu WM, Yang XH, Wang Y, Wang WG. 2010. Study on perfume stimulating olfaction with volatile oil of Acorus gramineus for treatment of the Alzheimer's disease rat. J Tradit Chin Med 30: 283–287.
- Liu H, Song Z, Liao DG, et al. 2015. Anticonvulsant and sedative effects of eudesmin isolated from Acorus tatarinowii on mice and rats. Phytother Res 29: 996–1003.
- Ma Y, Tian S, Sun L, et al. 2015. The effect of Acori Graminei Rhizoma and extract fractions on spatial memory and hippocampal neurogenesis in amyloid beta 1-42 injected mice. CNS Neurol Disord Drug Targets 14: 411–420.
- Rajput SB, Tonge MB, Karuppayil SM. 2014. An overview on traditional uses and pharmacological profile of Acorus calamus Linn. (Sweet flag) and other Acorus species. Phytomedicine 21: 268–276.
- Ryuk JA, Kim YS, Lee HW, Ko BS. 2014. Identification of Acorus gramineus, A. calamus, and A. tatarinowii using sequence characterized amplified regions (SCAR) primers for monitoring of Acori Graminei Rhizoma in Korean markets. Int J Clin Exp Med 7: 2488–2497.
- Schaeffer V, Meyer L, Patte-mensah C, Eckert A, Mensah-Nyagan AG. 2010. Sciatic nerve injury induces apoptosis of dorsal root ganglion satellite glial cells and selectively modifies neurosteroidogenesis in sensory neurons. Glia 58: 169–180.
- Tojima T, Kobayashi S, Ito E. 2003. Dual role of cyclic AMP-dependent protein kinase in neuritogenesis and synaptogenesis during neuronal differentiation. J Neurosci Res 74: 829–837.
- Vijayakumar KB, Bannimath G, Koganti VS, Iyer VB. 2016. Gas chromatographic method for analysis β-asarone in rhizome extracts of Acorus calamus and their microbiological evaluation. Pharm Methods 7: 121–126.
10.5530/phm.2016.7.18 Google Scholar
- Villegas R, Villegas GM, Núñez J, Hernández M, Castillo C. 2005. Neuron-like differentiation of PC12 cells treated with media conditioned by either sciatic nerves, optic nerves, or Schwann cells. Cell Mol Neurobiol 25: 451–461.
- Wei G, Fang YQ, Liu DH, Lin SF. 2004. Study on GC-MS fingerprint analysis in rhizome of volatile oil of Acorus tatarinowii. J Chin Mater Med 29: 764–768.
- Zhang H, Han T, Yu CH, Rahman K, Qin LP, Peng C. 2007. Ameliorating effects of essential oil from Acori Graminei Rhizoma on learning and memory in aged rats and mice. J Pharm Pharmacol 59: 301–309.
- Zhang X, Yi L, Deng B, et al. 2015. Discrimination of Acori Tatarinowii Rhizoma and Acori Calami Rhizoma based on quantitative gas chromatographic fingerprints and chemometric methods. J Sep Sci 38: 4078–4085.
- Zhou T, Xu B, Que H, Lin Q, Lv S, Liu S. 2006. Neurons derived from PC12 cells have the potential to develop synapses with primary neurons from rat cortex. Acta Neurobiol Exp 66: 105–112.
- Zhu Y, Duan X, Huang F, et al. 2016. Kai-Xin-San, a traditional Chinese medicine formula, induces neuronal differentiation of cultured PC12 cells: modulating neurotransmitter regulation enzymes and potentiating NGF inducing neurite outgrowth. J Ethnopharmacol 193: 272–282.