Content of saponin, tannin, and flavonoid in the leaves and fruits of Iranian populations from Rhamnus persica Boiss. (Rhamnaceae)

Yıl 2024, Cilt: 11 Sayı: 2, 235 - 243, 03.06.2024

Peymen Asadı Masoumeh Farasat Mehrnoush Tadayoni Neda Hassanzadeh Sina Attar Roshan

https://doi.org/10.21448/ijsm.1391683

Öz

To study the phytochemical properties in the leave and fruit of Iranian populations of Rhamnus persica Boiss, eighteen different populations from six geographical regions of Kermanshah province were studied. The results showed that the highest and lowest leaf saponin was present in Aliabad (6.40 mg/g) in Eslamabad-e Gharb and Chaharzebar in Mahidasht (3.29 mg/g), respectively. In fruit saponin, the highest content was in the population of Arkavazi in Eslamabad-e Gharb (4.33 mg/g) and the lowest being in Mahidasht population (Chaharzebar) and Sarpol-e Zahab (Galin) each with 2.20 mg/g. About the leaf tannin, the highest and lowest values were available in Barf-Abad population in Eslamabad-e Gharb (4.57 mg/g) and Chaharzebar in Mahidasht (1.83 mg/g), respectively. In addition, in the case of fruit tannin, the highest amount in Meleh-Sorkh population belonged to Homeil (2.74 mg/g) and the lowest being in of Changizeh population (Sonqor) in 2.28 mg/g. Moreover, the highest and lowest leaf flavonoids were obtained in two populations including Gordi in Eslamabad-e Gharb (6.14 mg/g) and Changizeh from Sonqor (4.09 mg/g), respectively. Regarding fruit flavonoids, the highest and lowest amounts were observed in populations of Meleh-Sorkh from Homeil (3.45 mg/g) and Banganjab in Mahidasht (2.13 mg/g). These findings confirmed the effect of geographical location on changing the phytochemical characteristics of Rhamnus populations in Kermanshah province from Iran.

Anahtar Kelimeler

Rhamnus persica, Phytochemical diversity, Saponin, Tannin, Flavonoid Population

Kaynakça

• Acharya, D., Mitaine-Offer, A.C., Kaushik, N., Miyamoto, T., Paululat, T., Mirjolet, J.F., Duchamp, O., & Lacaiile-Dubois, M.A. (2010) Steroidal saponins from Chlorophytum orchidastrum. Journal of Natural Products, 73, 7-11.
• Ahmed, J., Abu-Salim, K., Lim, L.B.L., & Jama, A.M. (2019) Evaluation of antioxidant activity and phytochemical screening of leaves, barks, stems and fruits of Alphitonia philippinensis (rhamnaceae) from Brunei Darussalam. Pharmacology Journal, 11(5), 951-961.
• Ahmed, R., Rashid, F., Ahmed, V.U., Mohammad, F.V., Noorwala, M., Bibi, N., & Kazmi, S.U. (2008). Saponins from the seeds of Achras sapota. Journal of Asian Natural Product Research, 10, 7-16.
• Ando, H., Fukumura, M., Hori, Y., Hirai, Y., Toriizuka, K., Kuchino, Y., & Ida, Y. (2008). Two new glucuronide saponins, achyranthosides G and H, from Achyranthes fauriei root. Journal of Natural Medicine, 62, 57-62.
• Faizal, A., & Geelen, D. (2013). Saponins and their role in biological processes in plants. Phytochemistry Review, 12, 877-893.
• Kimura, Y., Kobayashi, Y., Takeda, T. & Ogihara, Y. (1981). Three new saponins from the leaves of Hovenia dulcis (Rhamnaceae). Journal of Chemistry Society, 24, 1923-1927.
• Kohansal-Vajargah, S., Baradaran, R., Mosavi, S.G., Tolyat Abolhasani, M., &Yazdani, D. (2019). Evaluation and comparison of morphological and phytochemical characteristics of 14 Ziziphus jujuba Mill. ecotypes in Iran. Journal of Medicinal Plant, 7(1), 55-67.
• Kurylo, J.S., Knight, K.S., Stewart, J.R., & Endress, A.G. (2007). Rhmnus cathartica: native and naturalized distribution and habitat preferences. Journal of Torrey Botanical Society, 134(3), 420-430.
• Lila, M.A. (2004). Anthocyanins and Human Health: An in vitro investigative approach. Journal of Biomedical Biotechnology, 5, 306-313.
• Man, S., Gao, W., Zhang, Y., Huangc, L., & Liud, C. (2010). Chemical study and medical application of saponins as anti-cancer agents. Fitoterapia, 81(7), 703-714.
• Mubberley, D.I (1987). The plant book. Cambridge University Press.
• Murtala, M., Namadina, A., Nuhu, S., & ..., Ibrahim, S. (2019). Phytochemical screening, physicochemical properties and acute toxicity study of the leaves of Ziziphus abyssinica hochst. ex a. rich. (Rhamnaceae). FUDMA Journal of Science, 3(3), 102-108.
• Omidbeygi, R. (2008). Production and processing of medicinal plants. Institute Press Astan Qods Razavi. Mashhad, 347 pp.
• Paterson, A.H. (2019). Molecular dissection of complex traits. CRC press, New York.
• Pawlowska, A.M., Camangi, F., Bader, A. & Bracaa, A. (2009). Flavonoids of Zizyphus jujuba L. and Zizyphus spina-christi (L.) Willd (Rhamnaceae) fruits. Food Chemistry, 112(4), 858-862.
• Pormorad, F., Hosseinimehr, S. & Shahabimajd, N. (2016). Antioxidant activity, phenol and flavonoids of some selected Iranian medicinal plants. African Journal of Biotechnology, 5, 1142-1145.
• Ranjith, A. (2009). Phytochemical investigation on Sea buckthorn (Hipppophae rhamnoides L.) berries. Dissertation, National Institute for Interdisciplinary Science and Technology.
• Salehi, S.M.H., Aiynechi, Y., Amin, G.H. & Mahmoodi, Z. (1992). Survey for Iranian ponats for alkaloids and saponin, alkalodis and tanins. Journal of Pharmaceutical Science, 2(2-3), 1-11.
• Sattarian, A., Mahdiyani, S., & Habibi, M. (2017). Pollen morphology and endocarp studies of Rhamnus cathartica L., and Rhamnus pallasii Fisch. & CA Mey (Rhamnaceae) in North of Iran. Taxonomy and Biosystematics, 9(31), 43-60.
• Seri Seriab, C., Okpekon, T.A., Yao-Kouassia, P.A., Magid, A.A., Sayagh, C., Voutquenne-Nazabadiokob, L. (2020). Saponins and flavonoid glycosides from the leaves of Ziziphus mauritiana Lam native of a forest area of Ivory Coast. Phytochemistry Letter, 37, 5-9.
• Soufiyan, K.H., & Dinarvand, M. (2007). Flora of Iran, Rhamnaceae. Research Institute of Forests and Rangelands, Tehran.
• Tadesse, G., Reneela, P., & Dekebo, A. (2012). Isolation and characterization of natural products from Helinus mystachnus (Rhamnaceae). Journal of Chemical and Pharmaceutical Research, 4(3), 1756-1762.