Phytochemical Profiling and Pancreatic Lipase Inhibitory Activity of Flacourtia inermis Roxb. Fruits

Jump To References Section

Authors

  • Department of Pharmacy, FEAT, Annamalai University, Annamalai Nagar, Chidambaram - 608002, Tamil Nadu ,IN
  • Department of Pharmacy, FEAT, Annamalai University, Annamalai Nagar, Chidambaram - 608002, Tamil Nadu ,IN
  • Al Shifa College of Pharmacy, Keezhattur, Perinthalmanna, Malappuram – 679325, Kerala ,IN
  • Department of Pharmacy, FEAT, Annamalai University, Annamalai Nagar, Chidambaram - 608002, Tamil Nadu ,IN
  • Central Animal House, Rajah Muthiah Medical College, Annamalai University, Annamalai Nagar, Chidambaram – 608002, Tamil Nadu ,IN
  • Department of Pharmacy, FEAT, Annamalai University, Annamalai Nagar, Chidambaram - 608002, Tamil Nadu ,IN
  • Department of Pharmacy, FEAT, Annamalai University, Annamalai Nagar, Chidambaram - 608002, Tamil Nadu ,IN

DOI:

https://doi.org/10.18311/jnr/2023/32051

Keywords:

Chromatography, Flacourtia inermis, Mass Spectrometry, Obesity, Pancreatic Lipase, Phytochemicals, NMR

Abstract

Objectives: The present research work was carried out to explore the potential use Flacourtia inermis [FI] fruits for the prevention and treatment of obesity through pancreatic lipase inhibition in vitro. The study also aimed to investigate the chemical profiling of ethanol extract of FI using High-Performance Thin Layer Chromatography (HPTLC), High-Resolution Liquid Chromatography (HR-LC/MS), and Nuclear Magnetic Resonance Spectroscopy (NMR). Materials and Methods: Dried fruits of Flacourtia inermis were pulverised and subsequently extracted using various solvents in sequential steps of increasing polarity, such as hexane, ether, chloroform, ethyl acetate, ethanol, and water. After phytochemical analysis by preliminary chemical testing various extracts were evaluated for their ability to inhibit pancreatic lipase, and the ethanol extract was found to have an IC<sub>50</sub> close to that of reference drug orlistat. The most potent ethanol extract was analysed by HPTLC and separated through column chromatography, and further analysis was performed by HR-LC/MS and 1H-NMR techniques. Results: The presence of various phytoconstituents in this plant was detected using different types of analytical techniques. PL lipase inhibitory activity was observed in extracts in a dose dependent manner. Performing PL inhibition assay, it was found that the ethanol fruit extracts have lipase inhibitory activity with an IC<sub>50</sub> value of 377.15 μg/ml. HPTLC finger printing of the ethanol extract showed the presence of various bioactice compounds. HR-LC/MS study of the most active ethanol extract indicated the presence of different phytochemicals, such as phenolics and flavonoids. Column chromatographic separation of ethanol fruit extract of FI followed by structural elucidation using various spectral studies demonstrated the presence of two compounds namely myricetin and quinic acid. Conclusion: The study suggests that the edible fruits of Flacourtia inermis have the potential to inhibit pancreatic lipase enzyme and therefore, may be recommended for the management of obesity. Additionally, our research sheds light on the phytochemistry of flacourtia species and may lead to the development of novel chemical entities as potential pancreatic lipase inhibitors.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Downloads

Published

2023-06-13

How to Cite

Bency Baby, T., Murali, R., Suriyaprakash, T. N. K., Venkatachalam, V. V., Vigil Anbiah, S., Srinivasan, N., & Ajeesh, V. (2023). Phytochemical Profiling and Pancreatic Lipase Inhibitory Activity of <i>Flacourtia inermis</i> Roxb. Fruits. Journal of Natural Remedies, 23(2), 513–520. https://doi.org/10.18311/jnr/2023/32051

Issue

Section

Research Articles
Received 2022-11-24
Accepted 2023-04-21
Published 2023-06-13

 

References

Jo YH, Kim SB, Liu Q, Do SG, Hwang BY, Lee MK. Comparison of pancreatic lipase inhibitory isoflavonoids from unripe and ripe fruits of Cudraniatricuspidata. PLOS One. 2017; 12(3). https://doi.org/10.1371/journal.pone.0172069 PMID 28253267. DOI: https://doi.org/10.1371/journal.pone.0172069

Heck AM, Yanovski JA, Calis KA. Orlistat, a new lipase inhibitor for the management of obesity. Pharmacotherapy. 2000; 20(3):270-9. https://doi. org/10.1592/phco.20.4.270.34882 PMID 10730683. DOI: https://doi.org/10.1592/phco.20.4.270.34882

Liu TT, Liu XT, Chen QX, Shi Y. Lipase inhibitors for obesity: A review. Biomed Pharmacother. 2020; 128. https://doi.org/10.1016/j.biopha.2020.110314 PMID 32485574. DOI: https://doi.org/10.1016/j.biopha.2020.110314

Baby TB , Murali R , Suriyaprakash TNK , Srinivasan N. A review on pancreatic lipase inhibitors from natural sources: A potential target for obesity. Curr Enzyme Inhib. 2021; 17(2). https://doi.org/10.2174/1 573408017666210121114441 DOI: https://doi.org/10.2174/1573408017666210121114441

PannPhyu MP, Kongkatitham V, Mekboonsonglarp W, Likhitwitayawuid K, Sritularak B. Phenanthrenes from dendrobiumsenile and their pancreatic lipase inhibitory activity. J Asian Nat Prod Res. 2022; 24(7):697-702. https://doi.org/10.1080/10286020.202 1.1956478 DOI: https://doi.org/10.1080/10286020.2021.1956478

George G, Sridhar SNC, Paul AT. Investigation of synergistic potential of green tea polyphenols and orlistat combinations using pancreatic lipase assaybased synergy directed fractionation strategy. S Afr J Bot. 2020; 135:50-7. https://doi.org/10.1016/j. sajb.2020.08.009 DOI: https://doi.org/10.1016/j.sajb.2020.08.009

Nightingale SL. Orlistat approved for obesity. J Am Med Assoc. 1999; 281:1978. https://doi.org/10.1001/ jama.281.21.1978 DOI: https://doi.org/10.1001/jama.281.21.1978-a

Qi X. Review of the Clinical Effect of Orlistat; IOP ConfSer Mater Sci Eng. 2018; 301:012063. https://doi. org/10.1088/1757-899X/301/1/012063 DOI: https://doi.org/10.1088/1757-899X/301/1/012063

Filippatos TD, Derdemezis CS, Gazi IF, Nakou ES, Mikhailidis DP, Elisaf MS. Orlistat-associated adverse effects and drug interactions: A critical review. Drug Saf. 2008; 31(1):53-65. https://doi.org/10.2165/00002018-200831010-00005 PMID 18095746. DOI: https://doi.org/10.2165/00002018-200831010-00005

Lim TK. Edible medicinal and non-medicinal plants. Fruits. Springer Science+Business Media Dordrecht; 2013. https://doi.org/10.1007/978-94-007-5653-3_39 DOI: https://doi.org/10.1007/978-94-007-5628-1

Shibumon G, Benny P J, Sunny K, Cincy G, Sarala G. Antibiotic activity of 2, 3-dihydroxybenzoic acid isolated from Flacourtia inermis fruit against multidrug resistant bacteria. Asian J Pharm Clin Res. 2011; 4:126-30. https://doi.org/10.5958/j.0975-4261.3.3.038 DOI: https://doi.org/10.5958/j.0975-4261.3.3.038

Silaban YW, Suketi K, Susanto S, Matra DD. Isolation and characterization genes in lobi-lobi (Flacourtia inermis) related to sugar metabolism. IOP Conf Ser Earth Environ Sci. 2021; 694(1). https://doi. org/10.1088/1755-1315/694/1/012068 DOI: https://doi.org/10.1088/1755-1315/694/1/012068

Jayasinghe L, Lakdusinghe M, Hara N, Fujimoto Y. Phenolic constituents from the fruit juice of Flacourtia inermis. Nat Prod Res. 2012; 26(3):278- 81. https://doi.org/10.1080/14786419.2011.586638. PMID 21985676. DOI: https://doi.org/10.1080/14786419.2011.586638

Alakolanga AG, Kumar NS, Jayasinghe L, Fujimoto Y. Antioxidant property and [Formula: see text]- glucosidase, [Formula: see text]-amylase and lipase inhibiting activities of Flacourtia inermis fruits: Characterization of malic acid as an inhibitor of the enzymes. J Food Sci Technol. 2015; 52(12):8383-8. https://doi.org/10.1007/s13197-015-1937-6 PMID 26604419. DOI: https://doi.org/10.1007/s13197-015-1937-6

George S, Benny PJ. Antibacterial potency of fruit extracts of Flacourtia inermis against multidrugresistant strains and comparison of its activity with that of standard antibiotics. Int J Pharm. 2010; 1:95.

Khandelwal KR. Practical Pharmacognosy, techniques and experiments. 17thed, Nirali Prakashan. Pune; 2007. p. 149-53.

Zhang J, Kang MJ, Kim MJ, Kim ME, Song JH, Lee YM, et al. Pancreatic lipase inhibitory activity of Taraxacumofficinale in vitro and in vivo. Nutr Res Pract. 2008; 2(4):200-3. https://doi.org/10.4162/nrp.2008.2.4.200 PMID 20016719, PMCID PMC2788186. DOI: https://doi.org/10.4162/nrp.2008.2.4.200

Birari RB, Bhutani KK. Pancreatic lipase inhibitors from natural sources: Unexplored potential. Drug Discov Today. 2007; 12(19-20):879-89. https://doi.org/10.1016/j.drudis.2007.07.024 PMID 17933690. DOI: https://doi.org/10.1016/j.drudis.2007.07.024

Chanda J, Mukherjee PK, Biswas R, Malakar D, Pillai M. Study of pancreatic lipase inhibition kinetics and LC-QTOF-MS-based identification of bioactive constituents of Momordicacharantia fruits. Biomed Chromatogr. 2019; 33(4). https://doi.org/10.1002/bmc.4463 PMID 30536964. DOI: https://doi.org/10.1002/bmc.4463

Maqsood M, Ahmed D, Atique I, Malik W. Lipase inhibitory activity of Lagenariasiceraria fruit as a strategy to treat obesity. Asian Pac J Trop Med. 2017; 10(3):305-10. https://doi.org/10.1016/j.apjtm.2017.03.010 PMID 28442115. DOI: https://doi.org/10.1016/j.apjtm.2017.03.010

Nallappan D, Ong KC, Palanisamy UD, Chua KH, Kuppusamy UR. Myricetin derivative-rich fraction from Syzygiummalaccense prevents high-fat dietinduced obesity, glucose intolerance and oxidative stress in C57BL/6J mice [published online ahead of print, Aug 19 2020]. Arch Physiol Biochem. 2020:1- 12. https://doi.org/10.1080/13813455.2020.1808019 DOI: https://doi.org/10.1080/13813455.2020.1808019

Duangjai A, Nuengchamnong N, Suphrom N, Trisat K, Limpeanchob N, Saokaew S. Potential of coffee fruit extract and quinic acid on adipogenesis and lipolysis in 3T3-L1 adipocytes. Kobe J Med Sci. 2018; 64(3):E84-92. PMID 30666038.