Metabolomics-guided exploration of Pinus wallichiana A.B. Jacks. cones for antidiabetic compounds: Integrating in vitro, in silico, in vivo, and histopathological approaches
Main Article Content
Keywords
diabetes mellitus, Pinus wallichiana, GC-MS, antioxidant, molecular docking
Abstract
Pinus wallichiana A.B. Jacks., also known as Himalayan white pine, is recognized in traditional medicine for its various uses, including diabetes mellitus (DM). Pinus species like Pinus roxburghii (Chir pine) and Pinus gerardiana (Chilgoza pine) have shown promise for antidiabetic properties. This study focuses on the use of edible cones of Pinus wallichiana (P. wallichiana) for the potential management of DM. The methanolic extract of Pinus wallichiana (Pw.Cme) was subjected to Gas Chromatography–Mass Spectrometry (GC-MS) analysis, total phenolic content (TPC) and total flavonoid content (TFC) analyses, and qualitative phytochemical studies. The Pw.Cme and its derived fractions were evaluated for their in vitro antioxidant, α-glucosidase, α-amylase inhibitory studies, and the identified compounds were docked against enzyme targets, followed by Molecular Dynamic Simulation (MDS) studies. Detailed in vivo antidiabetic and histopathological studies were performed following standard procedures. The GC-MS analysis of Pw.Cme lead to identification of 45 compounds, and the Pinus wallichiana ethyl acetate (Pw.EtAc) fraction exhibited the highest TPC (258.55 mg gallic acid equivalent [GAE]/g) and TFC (63.05 mg quercetin equivalent [QE]/g). In 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) assays, the respective highest anti-radical activity was observed for Pw.EtAc, as IC50=13.0 µg/mL and 5.3 µg/mL. In enzymes inhibition studies, considerable α-amylase inhibition was observed for Pw.EtAc with IC50=1.98 µg/mL, and IC50=7.2 µg/mL for α-glucosidase. In vivo studies indicated that the administration of Pw.EtAc resulted in a marked decrease in fasting blood glucose levels, hyperlipidemia, and weight loss in diabetic albino mice. Histopathology of vital organs of albino mice, administered with various doses of Pw.EtAc showed a healing effect against alloxan-induced lesions in the heart, pancreas, liver, and kidneys. In conclusion, we can claim that the extract of P. wallichiana cones is rich in many phytocomponents and have potential antidiabetic properties.
References
Achi, N.K., and Ohaeri, O. 2015. GC-MS determination of bioactive constituents of the methanolic fractions of Cnidoscolus aconitifolius. Br J Pharm Res. 5(3):163. 10.9734/BJPR/2015/13893
Ahuja, J., Suresh, J., and Deep, A. 2011. Phytochemical screening of aerial parts of Artemisia parviflora. Der Pharm Lett. 3(6):116–124.
Akinjogunla, O., Yah, C., Eghafona, N., and Ogbemudia, F. 2010. Antibacterial activity of leave extracts of Nymphaea lotus (Nymphaeaceae) on methicillin resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Staphylococcus aureus (VRSA) isolated from clinical samples. Ann Biol Res. 1(2):174–184.
Arkkila, P.E., Koskinen, P.J., Kantola, I.M., Rönnemaa, T., Seppänen, E., and Viikari, J.S. 2001. Diabetic complications are associated with liver enzyme activities in people with type 1 diabetes. Diabetes Res Clin Pract. 52(2):113–118. 10.1016/S0168-8227(00)00241-2
BP, C., Chaware, V., Joshi, Y., and Biyani, K. 2009. Hepatoprotective activity of Hydroalcoholic extract of Momordica charantia Linn. leaves against carbon tetrachloride induced hepatopathy in rats. Inter. J ChemTech Res. 1(2):355–358.
Burroughs, A., and Westaby, D. 2005. Liver, biliary tract and pancreatic disease. In: Kumar, P., and Clarke (Eds.) Clinical Medicine, 6th Edn. pp. 347–418.
Chaturvedi, O., and Pandey, N. 2001. Genetic divergence in Bombax ceiba L. germplasms. Silvae Genet. 50(3–4):99–102.
Choi, C.W., Kim, S.C., Hwang, S.S., Choi, B.K., Ahn, H.J., Lee, M.Y., Park, S.H., and Kim, S.K. 2002. Antioxidant activity and free radical scavenging capacity between Korean medicinal plants and flavonoids by assay-guided comparison. Plant Sci. 163(6): 1161–1168. 10.1016/S0168-9452(02)00332-1
Dallakyan, S., and Olson, A.J. 2015. Small-molecule library screening by docking with PyRx. In Chemical biology: methods and protocols, pp. 243–250. New York, NY: Springer New York. 10.1007/978-1-4939-2269-7_19
Dar, M. Y., W. A., Shah, S, Mubashir and M. A. Rather 2012. Chromatographic analysis, anti-proliferative and radical scavenging activity of Pinus wallichina essential oil growing in high altitude areas of Kashmir, India. Phytomedicine 19(13): 1228–1233. 10.1016/j.phymed.2012.07.015
Edelman, S.V. 1998. Type II diabetes mellitus. Adv Intern Med. 43:449–500.
Eisenbarth, G.S. 1986. Type I diabetes mellitus. New Engl J Med. 314(21):1360–1368. 10.1056/NEJM198605223142106
Guex, N., and Peitsch, M.C. 1997. SWISS-MODEL and the Swiss-Pdb viewer: an environment for comparative protein modeling. Electrophoresis. 18(15):2714–2723. 10.1002/elps.1150181505
Hanwell, M.D., Curtis, D.E., Lonie, D.C., Vandermeersch, T., Zurek, E., and Hutchison, G.R. 2012. Avogadro: an advanced semantic chemical editor, visualization, and analysis platform. J Cheminform. 4(1):1–17. 10.1186/1758-2946-4-17
Hussain, F., Khan, Z., Jan, M.S., Ahmad, S., Ahmad, A., Rashid, U., Ullah, F., Ayaz, M., and Sadiq, A. 2019. Synthesis, in vitro. α-glucosidase inhibition, antioxidant, in vivo antidiabetic and molecular docking studies of pyrrolidine-2, 5-dione and thiazolidine-2, 4-dione derivatives. Bioorg Chem. 91:103128. 10.1016/j.bioorg.2019.103128
Kaul, K., Tarr, J.M., Ahmad, S.I., Kohner, E.M., and Chibber, R. 2013. Introduction to diabetes mellitus. Diabetes: an old disease, a new insight: pp. 1–11. 10.1007/978-1-4614-5441-0_1
Kodangala, C., Saha, S., and Kodangala, P. 2010. Phytochemical studies of aerial parts of the plant Leucas lavandulaefolia. Der Pharma Chemica. 2(5):434–437.
Kumar, N. 2015. Antioxidant and antibacterial properties of leaves of Elaeocarpus sphaericus Roxb., and Pinus wallichiana from Uttarakhand region of India. Int J Green Pharm (IJGP). 9(4). 10.22377/ijgp.v9i4.570
Linga Rao, M., and Savithramma, N. 2011. Phytochemical studies of Svensonia hyderobadensis (Walp.) mold: a rare medicinal plant. Der Pharm. Lett. 3:51–55.
Little, E.L., and Critchfield, W.B. 1969. Subdivisions of the Genus Pinus (Pines). Monograph. US Department of Agriculture, Forest Services, Washington, DC.
Mahnashi, M.H., Alqahtani, Y.S., Alqarni, A.O., Alyami, B.A., Jan, M.S., Ayaz, M., Ullah, F., Rashid, U., and Sadiq, A. 2021. Crude extract and isolated bioactive compounds from Notholirion thomsonianum (Royale) Stapf as multitargets antidiabetic agents: in vitro and molecular docking approaches. BMC Compl Med Ther. 21:1–13. 10.1186/s12906-021-03443-7
Maimoona, A., Naeem, I., Saddiqe, Z., Ali, N., Ahmed, G., and Shah, I. 2011. Analysis of total flavonoids and phenolics in different fractions of bark and needle extracts of Pinus roxburghii and Pinus wallichiana. J Med Plants Res. 5(13):2724–2728.
Malviya, N., Jain, S., and Malviya, S. 2010. Antidiabetic potential of medicinal plants. Acta Pol Pharm. 67(2):113–118.
Moss, D. 1975. Alkaline phosphatase isoenzymes. Tech Clin Aspects Enzyme. 20(1):20–34. 10.1159/000458916
Naeem, I., Taskeen, A., Mubeen, H., and Maimoona, A. 2010. Characterization of flavonols present in barks and needles of Pinus wallichiana and Pinus roxburghii. Asian J Chem. 22(1):41.
Nawaz, A., Sadiq, A., Bashir, N., Rashid, U., Ullah, F., Khan, S., Ullah, F., Khan, M.I., and Ayaz, M. 2025. Synthetic derivates of progesterone ameliorate scopolamine-induced cognitive deficits in animal models: antioxidant, enzyme inhibitory, molecular docking and behavioral correlates. Curr Neuropharmacol. 23(1):1797–1812. 10.2174/011570159X357722250212094900
Noor, A., Gunasekaran, S., Manickam, A.S., and Vijayalakshmi, M.A. 2008. Antidiabetic activity of Aloe vera and histology of organs in streptozotocin-induced diabetic rats. Curr Sci. 94(8):1070–1076.
Olokoba, A.B., Obateru, O.A., and Olokoba, L.B. 2012. Type 2 diabetes mellitus: a review of current trends. Oman Med J. 27(4):269. 10.5001/omj.2012.68
Pradeep, A., Dinesh, M., Govindaraj, A., Vinothkumar, D., and Ramesh Babu, N. 2014. Phytochemical analysis of some important medicinal plants. Int J Biol Pharm Res. 5(1):48–50.
Qadir, M., and Shah, W.A. 2014. Comparative GC-MS analysis, antioxidant, antibacterial and anticancer activity of essential oil of Pinus wallichaina from Kashmir, India. Elixir Appl Chem. 72:25819–25823.
Rahman, T.U., Uddin, G., Khattak, K.F., Liaqat, W., and Choudhary, M.I. 2016. Antibacterial, antifungal, insecticidal and phytotoxic activities of leaves of Pinus wallichiana. J Chem Pharm Res. 8(1):420–424.
Sabir, S., Akhtar, M.F., and Saleem, A. 2019. Endocrine disruption as an adverse effect of non-endocrine targeting pharmaceuticals. Environ Sci Pollut Res. 26:1277–1286. 10.1007/s11356-018-3774-4
Sabir, S., Saleem, A., Akhtar, M.F., Saleem, M., and Raza, M. 2018. Increasing beta cell mass to treat diabetes mellitus. Adv Clin Exp Med. 27(9):1309–1315. 10.17219/acem/74452
Sadiq, A., Zeb, A., Ullah, F., Ahmad, S., Ayaz, M., Rashid, U., and Muhammad, N. 2018. Chemical characterization, analgesic, antioxidant, and anticholinesterase potentials of essential oils from Isodon rugosus Wall. ex. Benth. Front Pharmacol. 9:623. 10.3389/fphar.2018.00623
Safhi, M.M., Alam, M.F., Sivakumar, S.M., and Anwer, T. 2019. Hepatoprotective potential of Sargassum muticum against STZ-induced diabetic liver damage in wistar rats by inhibiting cytokines and the apoptosis pathway. Anal. Cell Pathol. 1:7958701 10.1155/2019/7958701
Schulze, M.B., and Hu, F.B. 2022. Epidemiology of diabetes. In: Handbook of Epidemiology. Springer, New York, NY: NY: Springer, pp. 1–49. 10.1007/978-1-4614-6625-3_66-1
Singh, L., Dixit, P., Srivastava, R.P., Pandey, S., Verma, P.C., and Saxena, G. 2019. Ethnobotany and pharmacology of Pinus species growing naturally in Indian Himalayas: a plant review. Curr Pharm Biotechnol. 20(15):1281–1287. 10.2174/1389201020666190819153600
Vinci, G., D’Ascenzo, F., Maddaloni, L., Prencipe, S.A., and Tiradritti, M. 2022. The influence of green and black tea infusion parameters on total polyphenol content and antioxidant activity by ABTS and DPPH assays. Beverages. 8(2):18. 10.3390/beverages8020018
Wan Mohd Zain, W.Z., Ramli, N.N., Jusoh, S., and Hamid, N.A. 2021. Antioxidant activity, total phenolic and flavonoid content from leaves and seed extracts of Hevea brasiliensis clone. J Academia. 9:1–7.
Yamaguchi, M., and Weitzmann, M.N. 2009. The bone anabolic carotenoid β-cryptoxanthin enhances transforming growth factor-β1-induced SMAD activation in MC3T3 preosteoblasts. Int J Mol Med. 24(5):671–675. 10.3892/ijmm_00000278
Zheng, J.-S., Luan, J.A., Sofianopoulou, E., Sharp, S.J., Day, F.R., Imamura, F., Gundersen, T.E., Lotta, L.A., Sluijs, I and Stewart, I.D. 2020. The association between circulating 25-hydroxyvitamin D metabolites and type 2 diabetes in European populations: a meta-analysis and Mendelian randomisation analysis. PLoS Med. 17(10):e1003394. 10.1371/journal.pmed.1003394
Zulfqar, F., Akhtar, M.F., Saleem, A., Akhtar, B., Sharif, A., and Saleem, U. 2020. Chemical characterization, antioxidant evaluation, and antidiabetic potential of Pinus gerardiana (Pine nuts) extracts. J Food Biochem. 44(6):e13199. 10.1111/jfbc.13199

