CC BY-NC-ND 4.0 · Journal of Morphological Sciences 2018; 35(03): 153-160
DOI: 10.1055/s-0038-1669934
Original Article
Thieme Revinter Publicações Ltda Rio de Janeiro, Brazil

Effect of Potentilla Fulgens L. on Selected Enzyme Activities and Altered Tissue Morphology in Diabetic Mice

Suktilang Majaw
1   Department of Biotechnology & Bioinformatics, North-Eastern Hill University, Shillong, Meghalaya, India
,
Sooni Kerki Challam
1   Department of Biotechnology & Bioinformatics, North-Eastern Hill University, Shillong, Meghalaya, India
,
Donkupar Syiem
2   Department of Biochemistry, North-Eastern Hill University, Shillong, Meghalaya, India
› Author Affiliations
Further Information

Publication History

25 October 2017

23 July 2018

Publication Date:
02 October 2018 (online)

Abstract

Introduction The objective of the present study was to investigate the in vitro inhibitory effect of the Potentilla fulgens extract on amylase, α- and β-glucosidase, and lipase, as well as its effect on the ultrastructure of the liver, of the kidneys, and of the eye tissues in alloxan-induced diabetic mice. The present study was designed to get further insight regarding the action of P. fulgens from what has been previously known and reported about this plant.

Materials and Methods Roots of P. fulgens were extracted with 10 volumes of aqueous-methanol solution (1:4), and the prepared extract was used for in vitro inhibitory activity on amylase, α-glucosidase, β-glucosidase, and lipase. Afterwards, the plant extract was intraperitoneally administered for alternated days (250 mg/kg body weight) to diabetic mice for 4 weeks, and an ultrastructural examination of the liver, the kidneys and the eye tissues was performed using a transmission electron microscope (JEM-100 CX II, Jeol Ltd., Tokyo Japan).

Results The P. fulgens extract showed inhibitory activity against all the four enzymes (amylase, α- and β-glucosidase, and lipase), with the highest percentage of inhibition (94.57% ± 0.16 at 1 mg/mL) being observed against α-glucosidase when compared with the standard. The ultrastructural studies revealed a distortion in the structure of the nuclei and of the mitochondria in the kidneys and liver tissues of diabetic mice. Distortion of cell shape and disturbed orientation was observed in the eye lens of diabetic mice. The P. fulgens extract reversed/protected/reduced the ultrastructural alteration observed in the tissues (liver, kidney, and eye lens) of diabetic mice.

Conclusion The inhibitory effect of the P. fulgens extract against the aforementioned enzymes and its protective effect on the tissues of diabetic mice against alloxan-induced diabetes add further insight into the antidiabetic properties of this plant.

 
  • References

  • 1 Anwar F, Latif S, Ashraf M, Gilani AH. Moringa oleifera: a food plant with multiple medicinal uses. Phytother Res 2007; 21 (01) 17-25
  • 2 Verma S, Sharma H, Garg M. Phyllanthus amarus: A review. Journal of Pharmacognosy and Phytochemistry 2014; 3 (02) 8-22
  • 3 Gupta M, Sharma S, Gautam AK, Bhaduria R. Momordica charantia Linn (Karela): Nature's silent healer. Int J Pharm Sci Rev Res 2011; 11 (01) 32-37
  • 4 Tiwari P, Mishra BN, Sangwan NS. Phytochemical and pharmacological properties of Gymnema sylvestre: an important medicinal plant. BioMed Res Int 2014; 2014: 830285
  • 5 Zia-Ul-Haq M, Stanković MS, Rizwan K, Feo VD. Grewia asiatica L., a food plant with multiple uses. Molecules 2013; 18 (03) 2663-2682
  • 6 Syiem D, Syngai G, Khup PZ, Khongwir BS, Kharbuli B, Kayang H. Hypoglycemic effects of Potentilla fulgens L in normal and alloxan-induced diabetic mice. J Ethnopharmacol 2002; 83 (1-2): 55-61
  • 7 Syiem D, Syngai C, Kharbuli B, Kayang H, Khongwir BS. Anti-tumor activity of crude root extract of Potentilla fulgens . Indian Drugs 2003; 40: 124-125
  • 8 Syiem D, Khup PZ, Syiem AB. Effects of Potentilla fulgens Linn. on carbohydrate and lipid profiles in diabetic mice. Pharmacologyonline 2009; 2: 787-795
  • 9 Syiem D, Sharma R, Saio V. In vitro study of the antioxidant potential of some traditionally used medicinal plants of North-East India and assessment of their total phenolic content. Pharmacologyonline 2009; 3: 952-965
  • 10 Saio V, Syiem D, Sharma R, Dkhar J. Amelioration of age-dependent increase in oxidative stress markers in male mice by extract of Potentilla fulgens. Redox Rep 2016; 21 (03) 130-138
  • 11 Tangpu V, Deori K, Yadav AK. Evaluation of safety and protective effects of Potentilla fulgens root extract in experimentally induced diarrhea in mice. J Intercult Ethnopharmacol 2014; 3 (03) 103-108
  • 12 Koparal M, Ïrtegün S, Alan H, Deveci E, Gülsün B, Seker U. Effects of Potentilla fulgens as a prophylactic agent in tibial defects in rats. Anal Quant Cytopathol Histpathol 2016; 38 (02) 111-116
  • 13 Roy B, Swargiary A, Syiem D, Tandon V. Potentilla fulgens (Family Rosaceae), a medicinal plant of north-east India: a natural anthelmintic?. J Parasit Dis 2010; 34 (02) 83-88
  • 14 Kundu A, Ghosh A, Singh NK. , et al. Wound healing activity of the ethanol root extract and polyphenolic rich fraction from Potentilla fulgens . Pharm Biol 2016; 54 (11) 2383-2393
  • 15 Kaul K, Jaitak V, Kaul VK. Review on pharmaceutical properties and conservation measures of Potentilla fulgens Wall. ex Hook. – A medicinal endangered herb of higher Himalaya. Indian J Nat Prod Resour 2011; 2 (03) 298-306
  • 16 Choudhary A, Radhika M, Chatterjee A, Banerjee UC, Singh IP. Qualitative and quantitative analysis of Potentilla fulgens roots by NMR, matrix-assisted laser desorption/ionisation with time-of-flight MS, electrospray ionisation MS/MS and HPLC/UV. Phytochem Anal 2015; 26 (02) 161-170
  • 17 Jaitak V, Kaul VK. , Himlata, et al. New hopane triterpenes and antioxidant constituents from Potentilla fulgens . Nat Prod Commun 2010; 5 (10) 1561-1566
  • 18 Jaitak V, Sharma K, Kalia K. , et al. Antioxidant activity of Potentilla fulgens: An alpine plant of western Himalaya. J Food Compos Anal 2010; 23 (02) 142-147
  • 19 Syiem D, Majaw S. Effect of Potentilla fulgens L. aldose reductase activity of normal and diabetic mice. Inventi Rapid: Ethnopharmacology 2010; 1 (01) 13
  • 20 Majaw S, Syiem D. In vitro aldose reductase inhibitory potential of fractions isolated from Potentilla fulgens roots. J Appl Pharm Sci 2016; 6 (08) 102-109
  • 21 Syiem D, Majaw S. Effect of different solvent extracts of Potentilla fulgens L. on aldose reductase and sorbitol dehydrogenase in normoglycemic and diabetic mice. Pharmacologyonline 2011; 3: 63-72
  • 22 Syiem D, Majaw S. Effect of Potentilla fulgens L. methanolic extract on sorbitol dehydrogenase in normal and alloxan-induced diabetic mice. Pharmacologyonline 2010; 2: 671-680
  • 23 Kajaria D, , Ranjana, Tripathi J, Tripathi YB, Tiwari S. In-vitro α amylase and glycosidase inhibitory effect of ethanolic extract of antiasthmatic drug - Shirishadi. J Adv Pharm Technol Res 2013; 4 (04) 206-209
  • 24 Lowe ME. The triglyceride lipases of the pancreas. J Lipid Res 2002; 43 (12) 2007-2016
  • 25 Birari RB, Bhutani KK. Pancreatic lipase inhibitors from natural sources: unexplored potential. Drug Discov Today 2007; 12 (19-20): 879-889
  • 26 Ginsberg HN, Zhang YL, Hernandez-Ono A. Regulation of plasma triglycerides in insulin resistance and diabetes. Arch Med Res 2005; 36 (03) 232-240
  • 27 PS, Zinjarde SS, Bhargava SY, Kumar AR. Potent α-amylase inhibitory activity of Indian Ayurvedic medicinal plants. BMC Complement Altern Med 2011; 11: 5
  • 28 Cheng AY, Fantus IG. Oral antihyperglycemic therapy for type 2 diabetes mellitus. CMAJ 2005; 172 (02) 213-226
  • 29 Tiwari S. Plants: A rich source of herbal medicine. Journal of Natural Products 2008; 1: 27-35
  • 30 Kumar D, Ghosh R, Pal BC. α-glucosidase inhibitory terpenoids from Potentilla fulgens and their quantitative estimation by validated HPLC method. J Funct Foods 2013; 5: 1135-1141
  • 31 Harborne JB. Phytochemical methods. London and New York: Chapman and Hall; 1998
  • 32 Kim JS, Hyun TK, Kim MJ. The inhibitory effects of ethanol extracts from sorghum, foxtail millet and proso millet on α-glucosidase and α-amylase activities. Food Chem 2011; 124 (04) 1647-1651
  • 33 Sánchez-Medina A, García-Sosa K, May-Pat F, Peña-Rodríguez LM. Evaluation of biological activity of crude extracts from plants used in Yucatecan traditional medicine part I. Antioxidant, antimicrobial and beta-glucosidase inhibition activities. Phytomedicine 2001; 8 (02) 144-151
  • 34 Lin X, Xu B, Rui L. Pancreatic lipase inhibitory effects of mangosteen pericarps. Advance Journal of Food Science and Technology 2014; 6 (03) 284-291
  • 35 Ahmed D, Kumar V, Verma A, Shukla GS, Sharma M. Antidiabetic, antioxidant, antihyperlipidemic effect of extract of Euryale ferox salisb. with enhanced histopathology of pancreas, liver and kidney in streptozotocin induced diabetic rats. Springerplus 2015; 4: 315
  • 36 Varghese Z, Moorhead JF, Ruan XZ. The PPARalpha ligand fenofibrate: meeting multiple targets in diabetic nephropathy. Kidney Int 2006; 69 (09) 1490-1491
  • 37 Chang CLT, Lin Y, Bartolome AP, Chen YC, Chiu SC, Yang WC. Herbal therapies for type 2 diabetes mellitus: chemistry, biology, and potential application of selected plants and compounds. Evid Based Complement Alternat Med 2013; 2013: 378657
  • 38 Webster M, Witkin KL, Cohen-Fix O. Sizing up the nucleus: nuclear shape, size and nuclear-envelope assembly. J Cell Sci 2009; 122 (Pt 10): 1477-1486
  • 39 Rashid K, Das J, Sil PC. , et al. Taurine ameliorate alloxan induced oxidative stress and intrinsic apoptotic pathway in the hepatic tissue of diabetic rats. Food ChemToxicol 2013; 51: 317-329
  • 40 Das J, Sil PC. Taurine ameliorates alloxan-induced diabetic renal injury, oxidative stress-related signalling pathways and apoptosis in rats. Amino acids 2012; 43 (04) 1509-1523
  • 41 Cai L, Li W, Wang G, Guo L, Jiang Y, Kang YJ. Hyperglycemia-induced apoptosis in mouse myocardium: mitochondrial cytochrome C-mediated caspase-3 activation pathway. Diabetes 2002; 51 (06) 1938-1948
  • 42 Moley KH, Chi MM, Knudson CM, Korsmeyer SJ, Mueckler MM. Hyperglycemia induces apoptosis in pre-implantation embryos through cell death effector pathways. Nat Med 1998; 4 (12) 1421-1424
  • 43 Moley KH. Hyperglycemia and apoptosis: mechanisms for congenital malformations and pregnancy loss in diabetic women. Trends Endocrinol Metab 2001; 12 (02) 78-82
  • 44 Lemasters JJ, Nieminen AL, Qian T. , et al. The mitochondrial permeability transition in cell death: a common mechanism in necrosis, apoptosis and autophagy. Biochim Biophys Acta 1998; 1366 (1-2): 177-196
  • 45 Rodriguez-Enriquez S, He L, Lemasters JJ. Role of mitochondrial permeability transition pores in mitochondrial autophagy. Int J Biochem Cell Biol 2004; 36 (12) 2463-2472
  • 46 Stoka V, Turk B, Schendel SL. , et al. Lysosomal protease pathways to apoptosis. Cleavage of bid, not pro-caspases, is the most likely route. J Biol Chem 2001; 276 (05) 3149-3157
  • 47 Walvekar MV, Pol SB, Chandrasekhar Sagar BK. Histopathological and ultrastructural studies of the effect of fenugreek seed extract on pancreas of alloxan induced diabetic mice. Int J Pharmaceutical Sciences and Research 2014; 5 (07) 2960-2965
  • 48 Kinnally KW, Peixoto PM, Ryu SY, Dejean LM. Is mPTP the gatekeeper for necrosis, apoptosis, or both?. Biochim Biophys Acta 2011; 1813 (04) 616-622
  • 49 Kroemer G, Galluzzi L, Brenner C. Mitochondrial membrane permeabilization in cell death. Physiol Rev 2007; 87 (01) 99-163
  • 50 González-Polo RA, Boya P, Pauleau AL. , et al. The apoptosis/autophagy paradox: autophagic vacuolization before apoptotic death. J Cell Sci 2005; 118 (Pt 14): 3091-3102
  • 51 Kaniuk NA, Kiraly M, Bates H, Vranic M, Volchuk A, Brumell JH. Ubiquitinated-protein aggregates form in pancreatic beta-cells during diabetes-induced oxidative stress and are regulated by autophagy. Diabetes 2007; 56 (04) 930-939
  • 52 Sugiyama Y, Lovicu FJ, McAvoy JW. Planar cell polarity in the mammalian eye lens. Organogenesis 2011; 7 (03) 191-201
  • 53 Heys KR, Cram SL, Truscott RJW. Massive increase in the stiffness of the human lens nucleus with age: the basis for presbyopia?. Mol Vis 2004; 10: 956-963
  • 54 Joy A, Currie MS, Donohue ST, Al-Ghoul KJ. Aberrant basal fiber end migration underlies structural malformations in a streptozotocin-induced diabetic rat model. Exp Eye Res 2009; 89 (03) 344-357
  • 55 Ragawan B, Krishnakumari S. Effect of T. arjuna stem bark extract on histopathology of liver, kidney and pancreas of alloxan-induced diabetic rats. Asian J Biomed Res 2006; 9: 189-197