Comparative Chemical Composition and Acetylcholinesterase (AChE) Inhibitory Potential of Cinnamomum camphora and Cinnamomum tamala.
C. camphora
C. tamala
acetylcholinesterase
essential oils
physostigmine
Journal
Chemistry & biodiversity
ISSN: 1612-1880
Titre abrégé: Chem Biodivers
Pays: Switzerland
ID NLM: 101197449
Informations de publication
Date de publication:
Aug 2023
Aug 2023
Historique:
received:
09
05
2023
accepted:
17
07
2023
medline:
24
8
2023
pubmed:
3
8
2023
entrez:
3
8
2023
Statut:
ppublish
Résumé
Cinnamomum species have applications in the pharmaceutical and fragrance industry for wide biological and pharmaceutical activities. The present study investigates the chemical composition of the essential oils extracted from two species of Cinnamomum namely C. tamala and C. camphora. Chemical analysis showed E-cinnamyl acetate (56.14 %), E-cinnamaldehyde (20.15 %), and linalool (11.77 %) contributed as the major compounds of the 95.22 % of C. tamala leaves essential oil found rich in phenylpropanoids (76.96 %). C. camphora essential oil accounting for 93.57 % of the total oil composition was rich in 1,8-cineole (55.84 %), sabinene (14.37 %), and α-terpineol (10.49 %) making the oil abundant in oxygenated monoterpenes (70.63 %). Furthermore, the acetylcholinesterase inhibitory activity for both the essential oils was carried out using Ellman's colorimetric method. The acetylcholinesterase inhibitory potential at highest studied concentration of 1 mg/mL was observed to be 46.12±1.52 % for C. tamala and 53.61±2.66 % for C. camphora compared to the standard drug physostigmine (97.53±0.63 %) at 100 ng/ml. These multiple natural aromatic and fragrant characteristics with distinct chemical compositions offered by Cinnamon species provide varied benefits in the development of formulations that could be advantageous for the flavor and fragrance industry.
Identifiants
pubmed: 37533252
doi: 10.1002/cbdv.202300666
doi:
Substances chimiques
Acetylcholinesterase
EC 3.1.1.7
Oils, Volatile
0
Pharmaceutical Preparations
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202300666Subventions
Organisme : Central Institute of Medicinal and Aromatic Plants
ID : HCP007
Informations de copyright
© 2023 Wiley-VHCA AG, Zurich, Switzerland.
Références
S. Kumar, R. Kumari, S. Mishra, J. Pharm. Pharmacol. 2019, 71,1735-1761.
P. Ranasinghe, R. Jayawardana, P. Galappaththy, G. R. Constantine, N. de Vas Gunawardana, P. Katulanda, Diabet Med. 2012, 29, 1480-1492.
N. Singh, A. S. Rao, A. Nandal, S. Kumar, S. S. Yadav, S. A. Ganaie, B. Narasimhan, Food Chem. 2021, 338, 127773.
V. Sharma, L. J. M. Rao, Crit. Rev. Food Sci. Nutr. 2014, 54, 433-448.
M. Shah, M. Panchal, Int J Pharm Sci Rev Res. 2010, 5, 141-144.
R. K. Upadhyay, Research Reviews: Pharm. Pharm. Sci. 2017, 6, 18-28.
A. K. Pandey, A. K. Mishra, A. Mishra, Cell. Mol. Biol. 2012, 58, 142-147.
J. K. Chaurasia, Y. B. Tripathi, Immunopharmacol. Immunotoxicol. 2011, 33, 466-472.
S. H. Lee, D. S. Kim, S. H. Park, H. Park, Molecules. 2022, 27, 2695.
V. S. Pragadheesh, A. Saroj, A. Yadav, C. S. Chanotiya, M. Alam, A. Samad, Ind. Crops Prod. 2013, 49, 628-633.
H. J. Lee, E. A. Hyun, W. J. Yoon, B. H. Kim, M. H. Rhee, H. K. Kang, J. Y. Cho, E. S. Yoo, J. Ethnopharmacol. 2006, 103, 208-216.
R. Hamidpour, S. Hamidpour, M. Hamidpour, M. Shahlari, Int J Case Rep Images. 2013, 4, 86-89.
S. Guo, Z. Geng, W. Zhang, J. Liang, C. Wang, Z. Deng, S. Du, Int. J. Mol. Sci. 2016, 17, 1836.
S. Xiao, H. Yu, Y. Xie, Y. Guo, J. Fan, W. Yao, J. Ethnopharmacol. 2021, 267, 113516.
Y. Xu, J. Qin, P. Wang, Q. Li, S. Yu, Y. Zhang, Y. Wang, Rev. Soc. Bras. Med. Trop. 2020, 53, e20190211.
M. Wu, L. Ni, H. Lu, H. Xu, S. Zou, X. Zou, J. Chem. 2020, 1-14.
D. Kennedy, E. Okello, P. Chazot, M. J. Howes, S. Ohiomokhare, P. Jackson, C. Haskell-Ramsay, J. Khan, J. Forster, E. Wightman, Nutrients 2018, 10, 1029.
P. F. D. Oliveira, J. M. Alves, J. L. Damasceno, R. A. M. Oliveira, H. Dias Júnior, A. E. M. Crotti, D. C. Tavares, Rev. Bras. Farmacogn. 2015, 25, 183-188.
J. Reichling, P. Schnitzler, U. Suschke, R. Saller, Complement Med Res. 2009, 16, 79-90.
Z. Aumeeruddy-Elalfi, N. Lall, B. Fibrich, A. B. Van Staden, M. Hosenally, M. F. Mahomoodally, J. Food Drug Anal. 2018, 26, 232-243.
P. Srivastava, S. Mohanti, D. U. Bawankule, F. Khan, K. Shanker, Naunyn-Schmiedeberg′s Arch. Pharmacol. 2014, 387, 119-127.
M. B. Colovic, D. J. Krstic, T. D. Lazarevic-Pasti, A. M. Bondzic, V. M. Vasic, Curr. Neuropharmacol. 2013, 11, 315.
Jyotshna, N. Srivastava, B. Singh, D. Chanda, K. Shanker, Pharm. Biol. 2015, 53, 1677-1683.
A. Abd Rashed, A. Z. Abd Rahman, Molecules 2021, 26, 1107.
S. H. Al-Mijalli, H. N. Mrabti, H. Ouassou, R. Flouchi, E. M. Abdallah, R. A. Sheikh, M. M. Alshahrani, A. A. A. Awadh, H. Harhar, N. E. Omari, A. Qasem, Life 2022, 12, 1876.
S. Afzal, B. A. Chaudhry, A. Ahmad, M. Uzair, K. Afzal, Antioxidant Pharmacogn. Mag. 2017, 13, 647.
S. M. Aljubiri, E. A. Elsalam, F. K. Abd El Hady, M. O. Radwan, A. I. Almansour, K. H. Shaker, Z. Naturforsch. C 2023, 78, 209-216.
J. P. Dzoyem, A. T. Tsamo, R. Melong, P. Mkounga, A. E. Nkengfack, L. J. McGaw, J. N. Eloff, Biol. Res. 2015, 48, 1-6.
E. R. Laili, W. Ekasari, N. Nuengchamnong, N. Suphrom, Adv. Pharmacol. Pharm. Sci. 2023.
M. A. Farag, S. M. Ezzat, M. M. Salama, M. G. Tadros, R. A. Serya, Z. Naturforsch. C 2016, 71, 393.
H. Jiang, J. Wang, L. Song, X. Cao, X. Yao, F. Tang, Y. Yue, Molecules. 2016, 21, 423.
D. K. Poudel, A. Rokaya, P. K. Ojha, S. Timsina, R. Satyal, N. S. Dosoky, P. Satyal, W. N. Setzer, Molecules 2021, 26, 5132.
Q. Ling, B. Zhang, Y. Wang, Z. Xiao, J. Hou, C. Xiao, Y. Liu, Z. Jin, Molecules 2022, 27, 7356.
T. Zhang, Y. Zheng, C. Fu, H. Yang, X. Liu, F. Qiu, X. Wang, Z. Wang, Molecules 2023, 28, 973.
C. Lv, L. Hao, X. Cui, F. Yi, C. Su, Chem. Biodiversity 2021, 18, e2100201.
A. Ahmed, M. I. Choudhary, A. Farooq, B. Demirci, F. Demirci, K. H. Can Başer, Flavour Fragrance J. 2000, 15, 388-390.
S. R. Mir, M. Ali, R. Kapoor, Flavour Fragrance J. 2004, 19, 112-114.
V. Singh, A. K. Gupta, S. P. Singh, A. Kumar, Sci. World J. 2012.
W. M. N. H. W. Salleh, F. Ahmad, K. H. Yen, Nat. Prod. Commun. 2015, 10.
J. Malik, K. Munjal, R. Deshmukh, J. Basic Clin. Physiol. Pharmacol. 2015, 26, 275-285.
M. Mutlu, Z. Bingol, E. M. Uc, E. Köksal, A. C. Goren, S. H. Alwasel, I. Gulcin, Life 2023, 13, 136.
P. R. Ribeiro, M. F. D. C. Neto, E. A. Chagas, P. C. Cardoso, J. A. Takahashi, A. C. G. R. De Melo, R. C. Dos Santos, A. A. De Melo Filho, Chem Eng Trans. 2019, 75, 361-366.
M. K. Dalai, S. Bhadra, S. K. Chaudhary, A. Bandyopadhyay, P. K. Mukherjee, Indian J. Tradit. Know. 2014, 13, 691-697.
C. R. Kim, S. J. Choi, J. K. Kim, C. K. Park, M. C. Gim, Y. J. Kim, G. G. Park, D. H. Shin, Biol. Pharm. Bull. 2017, 40, 932-935.
C. R. Kim, S. J. Choi, Y. K. Kwon, J. K. Kim, Y. J. Kim, G. G. Park, D. Shin, Biol. Pharm. Bull. 2016, 39, 1130-1136.
M. H. Mahnashi, B. A. Alyami, Y. S. Alqahtani, A. O. Alqarni, M. S. Jan, M. Ayaz, F. Ullah, M. Shahid, U. Rashid, A. Sadiq, BMC Complement. Med. 2021, 21, 1-14.
B. S. Jugreet, S. K. Ibrahime, G. Zengin, H. H. Abdallah, M. F. Mahomoodally, Chem. Biodiversity 2021, 18, e2000921.
A. B. Mohammed, S. Yagi, T. Tzanova, H. Schohn, H. Abdelgadir, A. Stefanucci, A. Mollica, M. F. Mahomoodally, T. A. Adlan, G. Zengin, S. Afr. J. Bot. 2020, 132, 403-409.
M. S. Kang, J. H. Park, H. S. Lee, Exp. Appl. Acarol. 2022, 86, 313-326.
D. Alimi, A. Hajri, S. Jallouli, H. Sebai, Vet. Parasitol. 2022, 309, 109743.
European Pharmacopoeia, 4th ed. Version 4.08. European Directorate for the Quality of Medicine and Healthcare, Strasbourg: EDQM. 2004.
R. P. Adams, Identification of essential oil components by gas chromatography/mass spectrometry, Allured Publishing Corporation, Carol Stream, IL, USA, 2007.
G. L. Ellman, K. D. Courtney, J. J. Andres, R. M. Feather-Stone, Biochem. Pharmacol. 1961, 7, 88-95.