Pterocarpus Marsupium for the Treatment of Diabetes and Other Disorders
Dhayaney Vijayan and Sibi G*
Department of Biotechnology, Indian Academy Degree College-Autonomous, India
Submission: January 24, 2019; Published: March 01, 2019
*Corresponding author: Sibi G, Head of the Department, Department of Biotechnology, Indian Academy Degree College-Autonomous, Bangalore, India
How to cite this article: Dhayaney V, Sibi G. Pterocarpus Marsupium for the Treatment of Diabetes and Other Disorders. J Complement Med Alt 006 Healthcare. 2019; 9(1): 555754. DOI:10.19080/JCMAH.2019.09.555754
Abstract
Pterocarpus marsupium Roxb., is a deciduous tree commonly grows in India and Sri Lanka. It is well known to Ayurvedic medicine because of its curative and lenitive properties. The heartwood extract of P. marsupium is reported to have many pharmacological compounds and used in treatment of various disorders. Literature was collected via electronic search (PubMed, ScienceDirect) from published articles that reports medicinal properties of P. marsupium. A significant research of antidiabetic activities and other medicinal properties of P. marsupium combined with bioactive compounds isolated from the plant will provide leads for the discovery of new drugs for the management of many disorders with minimal side effects.
Keywords: Pterocarpus marsupium; Vijayasar; Anti-diabetic; Antioxidant
Introduction
Diabetes is a chronic disorder of carbohydrate, fat and protein metabolism characterized by increased fasting and post prandial blood sugar levels. The increasing worldwide incidence of diabetes mellitus in adults constitutes a global public health burden. Out of the two types of diabetes, the incidence of non-insulin dependent diabetes mellitus is much higher than the insulin dependent diabetes mellitus. Even insulin therapy does not reinstate a permanent normal pattern of glucose homeostasis and carries an increased risk of atherogenesis and hypoglycemia. Plants are used as traditional remedies in one or other form for the treatment of diabetes. There has been an exponential growth in the field of herbal medicine and these drugs are gaining popularity both in developing and developed countries because of their natural origin and less side effects. Drugs derived from natural products have played a major role in the development of pharmaceutical treatments for diabetes.Pterocarpus marsupium Roxb., is a deciduous tree commonly grows in Sri Lanka and India [1]. It is popularly known as Vijaysar in Hindi and is a valuable medicinal plant, used mainly in Ayurveda, for the treatment of diabetes [2-4]. It is well known to Ayurvedic medicine because of its curative and lenitive properties. Its flowers are employed against fever, its heartwood as depurative, hemostatic, and rejuvenating, its wood is used for chest and body pain as well as indigestion, etc. The gum (kino) obtained from the tree is used in diarrhea, pyrosis and toothache. Bruised leaves are used externally for boils, sores, and various skin diseases. The water kept in tumblers made out of the wood of this plant is said to be beneficial for chest pain and diabetes. The bark of P. marsupiumis very effective in preventing cataract formation and reducing hyperglycemia in alloxanized diabetic rats [1] and the heartwood is useful as hypolglycemic agents [5].
Methodology
A systematic search was carried out in Pub Med, Scopus and Web of Sciences using a combination of Boolean operators. Peer reviewed papers in English on the keyword Pterocarpus marsupium were retrieved and evaluated based on titles and abstracts. The retrieved papers were managed using Mendeley and the data were consolidated.
Anti-diabetic activity
Aqueous extract of heartwood of Pterocarpus marsupium was given orally to alloxan induced type-2 diabetic rabbit model (Pradhan et al., 2017). Both the fasting blood glucose (194.8±12.7 vs. 155.2±16.3) and postprandial blood glucose (191.6±23.2 vs. 149.2±14.5) were decreased indicating the hypoglycaemic effect of P. marsupium. Incubation of red blood cells with glucose in the presence of alcoholic extract of P. marsupium under high glucose conditions lead to reduction in the accumulation of intracellular sorbitol in a dose dependent manner. There was 50% reduction of sorbitol accumulation with alcoholic extract of was observed with IC50 151.00μg/ml and 105.12μg/ml for ascorbic acid [6]. Ethanolic extract of P. marsupium heartwood have antihyperglycemic activity in streptozotocin treated diabetic rats [7]. At 100 mg/kg dose levels, fasting blood glucose, oral glucose tolerance and serum insulin levels were recorded as 113±3.40mg/dl, 35930±102.9AUC and 160±31.3ng/l respectively. Blood glucose lowering effect of P. marsupium heartwood was also reported. Antidiabetic activity of P. marsupium Roxb. heartwood in alloxan induced diabetic rats using extracts obtained by optimized conventional and non-conventional extraction methods was evaluated by Devgan et al. [8]. Ultrasound-assisted extraction was proved to enhance the antidiabetic activity of P. marsupium. Mohan Kumar et al. [9] reported that the exposure of mouse pancreatic and muscle tissues to P. marsupium extract stimulated the insulin secretion and glucose uptake, respectively, in a concentration-dependent manner. Gairola et al. [10] found that the aqueous extract significantly reduces type 2 diabetes in rats and can prevent hyperinsulinemia and hypertriglyceridemia. Aqueous extract of P. marsupium has significantly decreased the fasting blood glucose (182.5±4.1mg/dL) in type 2 diabetic rat. It also decreased the postprandial hyperglycemia significantly (112.3±2.8mg/dL) as compared to diabetic control group (301.4±5mg/dL). P.marsupium modulated the inflammatory cytokine TNF-α in type 2 diabetic rats [11]. Dhanabal et al. [12] studied the antidiabetic activity of various subfractions of the alcohol extract of the bark of Pterocarpus marsupium Roxb. in alloxan-induced diabetic rats. The butanol subfraction of the alcohol extract of P. marsupium exhibits significant antidiabetic activity and corrects the metabolic alterations in diabetic rats. Mukhtar et al. [13] reported the hypoglycemic activity of P. marsupium wood at an oral dose of 250mg/kg in alloxan induced diabetic rats. The aqueous extract of P. marsupium significantly (P<0.001) reduced the blood sugar levels from 72.32±5.62 to 61.35±1.2mg% 2 h after oral administration of the extract and also significantly lowered the blood glucose in alloxan diabetic rats from 202.91±5.44 to 85.22±11.28mg% 21 days after daily oral administration of the extract [14]. Alloxan-diabetic rats fed with the ethanolic extract of P. marsupium wood for 5 days resulted in a significant lowering of fasting blood sugar level. There was a 5-fold increase in blood glucose level of alloxan to rats after injection compared to normal controls and feeding of the extract to alloxan-diabetic animals lowered the blood sugar by 70% as compared to the alloxan-diabetic controls [15].
Antioxidant activity
Many recent studies reveal that antioxidants capable of neutralizing free radicals are effective in preventing experimentally induced diabetes in animal models. In DPPH scavenging activity and ABTS∙+ scavenging activity, IC50 values were found to be 138.3, 12.4, 13.5 and 47.8, 3.9, 4.2μg/mL for aqueous, methanolic extract of P. marsupium and standard ascorbic acid respectively. In α-amylase inhibition assay and α-glucosidase inhibition assay, IC50 values for standard Acarbose, aqueous and methanolic extract of heartwood were 44.09, 166.72, 48.20 and 45.17, 172.32, 48.12 respectively [16]. The effects of different fractions of heart wood of Pterocarpus marsupium on antioxidant enzyme like protein thiols and the efficacy of the extract for the protection of the renal function in alloxan induced diabetic rats was evaluated by Bhata, Nayak [17]. P. marsupium extract showed a promising antioxidant effect, as well as hypoglycemic activity. Aqueous extract of P. marsupium showed high antioxidant activity in all different assays used and also protected mitochondria against oxidative damage. It significantly reduced lactate dehydrogenase release along with reduction of lipid peroxidation [18]. The herbal extract mixture of P. marsupium and O. sanctum has succeeded in not only rectifying dyslipidemia but also in restoring the endogenous antioxidant levels to the pre-diabetic status in non-diabetic and alloxan induced diabetic adult female Wistar rats [19].
Anticancer activity
The cytotoxicity of P. marsupium aqueous extract was evaluated by Gosetti et al. [20] using calcein acetoxymethyl ester (calcein-AM) assays. Different cell lines were incubated for 24h with different concentrations of the aqueous heartwood extract. The IC50 values for cancer cells are comparable among the cell lines and are significantly lower (at least 50%) for the cancer cell lines than for non-tumoral cell lines, highlighting a selective cytotoxicity of the extract towards the cancer cells. α-dihydroxychalcone-glycoside (α-DHC) isolated from P. marsupium has effectively reduced nitric oxide and cytokine production by the LPS stimulated RAW 264.7 mouse macrophage cell line. The compound effectively attenuated the expression of inflammation-mediating enzymes COX-2 and iNOS at the mRNA as well as protein levels in a concentration dependent manner [21]. Pterostilbene isolated from P. marsupium was found to cause apoptosis in breast (MCF-7) and prostate (PC3) cancer cell lines. It also inhibited Matrix metalloproteinase 9 (MMP9) and α-methylacyl-CoA recemase (AMACR), two very well-known metastasis inducers [22].
Reproductive effects
Hugar et al. [23] has reported that Pterocarpus marsupium showed potential reproductive effects on testosterone propionate induced Polycystic Ovary Syndrome (PCOS) female albino rats and could be used as an alternative therapy in the treatment of PCOS.
Activity against cataract
The protective effect of Pterocarpus marsupium bark extracts against cataract in streptozotocin-induced diabetic male albino rats was investigated by Xu et al. [24]. The blood glucose was reduced up to 36% following treatment with bark extracts. The blood insulin and tissue GSH contents were substantially increased more than 100% in diabetic rats following treatment with extracts. Aldose reductase activity was reduced up to 79.3% in diabetic rats following treatment with extracts. he findings concluded that the use of P. marsupium bark extracts could be the potential therapeutic approach for the reduction of aldose reductase against diabetic cataract.
Activity against Ulcerative colitis
The effect of P. marsupium on acetic acid induced ulcerative
colitis in rats was studied by Mathew et al. [25]. P. marsupiumhad
significantly reduced colon inflammation and mucosal
damage in the treated group. The COX-1/2 selective inhibitory
activity of P. Marsupium (PM) extract was investigated by Hougee
et al. [26]. PM extract, pterostilbene and resveratrol inhibited
PGE2 production from LPS-stimulated human Peripheral Blood
Mononuclear Cells (PBMC) with IC50 values of 3.2 +/- 1.3 microg/
mL, 1.0 +/- 0.6 micro M and 3.2 +/- 1.4 micro M, respectively. In
a COX-1 Whole Blood Assay (WBA) PM extract was not effective
while in a COX-2 WBA, PM extract decreased PGE2 production
indicating COX-2 specific inhibition (Table 1 & Table 2) [27-56].


Conclusion
Major hindrance in amalgamation of herbal medicine in
modern medical practices is lack of scientific and clinical data
proving their efficacy and safety. This review article showed the
anti-diabetic potential of a P. Marsupium for the management of
hyperglycemia, along with good antioxidant activity. However
limited data were available about the collective pharmaceutical
property of P. Marsupium. This plant may provide leads for the
discovery of new drugs for the management of many disorders
with minimal side effects.
References
- Therrell MD, Stahle DW, Mukelabai MM, Shugart HH (2007) Age, and
radial growth dynamics of Pterocarpus angolensis in southern Africa.
For Ecol Manage 244: 24-31.
- Chatterjee A, Pakrashi SC (1991) The treatise on Indian medicinal
plants: vol. 1. New Delhi: Publications and Information Directorate,
CSIR 172p.-illus., col. illus. ISBN 8172360118 En Icones. Includes authentic
Sanskrit slokas in both Devnagri and Roman scripts. Plant Rec
Geogr: 6.
- Satyavati GV, Gupta AK, Tandon N (1987) Med Plants India 27: 574-575.
- Satyavati GV, Neeraj T, Madhu S (1989) Indigenous plant drugs for diabetes
mellitus. Indian J Diabetes Dev Countries: 1-35.
- Sheehan EW, Zemaitis MA, Slatkin DJ, Schiff (1983) A constituent of
Pterocarpus marsupium, (-)-epicatechin, as a potential antidiabetic
agent. J Nat Prod 46 (2): 232-234.
- Gupta P, Jain V, Pareek A, Kumari P, Singh R, et al. (2017) Evaluation
of effect of alcoholic extract of heartwood of Pterocarpus marsupium
on in vitro antioxidant, anti-glycation, sorbitol accumulation and
inhibition of aldose reductase activity. J Tradit Complement Med 7(3):
307-314.
- Mishra A, Srivatsava R, Srivatsava SP, Gautam S, Tamrakar AK, et al.
(2013) Antidiabetic activity of heartwood of Pterocarpus marsupium
Roxb. and analysis of phytoconstituents. Indian Journal of Experimental
Biology 51(5): 363-374.
- Devgan M, Nanda A, Ansari SH (2013) Comparative evaluation of the
anti-diabetic activity of Pterocarpus marsupium Roxb. heartwood in alloxan
induced diabetic rats using extracts obtained by optimized conventional
and non-conventional extraction methods. Pak J Pharm Sci
26(5): 973-976.
- Mohan Kumar SK, Oshea T, McFarlane JR (2012) Insulinotrophic and
insulin-like effects of a high molecular weight aqueous extract of Pterocarpus
marsupium Roxb. hardwood. Journal of Ethnopharmacology
141(1): 72-79.
- Gairola S, Gupta V, Baljinder S, Mukesh M, Parveen B (2010) Phytochemistry
and pharmacological activities of Pterocarpus marsupium – a
review. Int Res J Pharm 1: 100-104.
- Halagappa K, Girish HN, Srinivasan BP (2010) The study of aqueous
extract of Pterocarpus marsupium Roxb. on cytokine TNF-α in type 2diabetic rats. Indian Journal of pharmacology 42(6): 392-396.
- Dhanabal SP, CK Kokate, Ramanathan M, Kumar EP, Suresh B (2005)
Hypoglycaemic activity of Pterocarpus marsupium Roxb. Phytother Res
20(1): 4-8.
- Mukhtar HM, Ansari SH, Ali M, Bhat ZA, Naved T (2006) Effect of aqueous
extract of Pterocarpus marsupium wood on alloxan-induced diabetic
rats. Pharmazie 60(6): 478-479.
- Vats V, Grover JK, Rathi SS (2002) Evaluation of antihyperglycemic and
hypoglycemic effect of Trigonella foenum-graecum Linn, Ocimum sanctum
Linn and Pterocarpus marsupium Linn in normal and alloxanized
diabetic rats. J Ethnopharmacol 79(1): 95-100.
- Ahmad F, Khalid P, Khan MM, Chaubey M, Rastogi K, et al. (1991) Hypoglycemic
activity of Pterocarpus marsupium wood. Journal of Ethnopharmacology
35(1): 71-75.
- Yadav VK, Mishra A (2018) In vitro and in silico study of hypoglycemic
potential of Pterocarpus marsupium heartwood extract. Nat Prod Res:
1-5.
- Bhata V, Nayak BS (2015) Renoprotective effects, protein thiols and
liver glycogen content of alloxan-induced diabetic rats treated with
different fractions of heartwood of Pterocarpus marsupium. Nat Prod
Commun 10(11): 1843-1846.
- Mohammadi M, Khole S, Devasagayam TP, Ghaskadbi SS (2009) Pterocarpus
marsupium extract reveals strong in vitro antioxidant activity.
Drug Discov Ther 3(4): 151-161.
- Singh PK, Baxi D, Banerjee S, Ramachandran AV (2012) Therapy with
methanolic extract of Pterocarpus marsupium Roxb and Ocimum sanctum
Linn reverses dyslipidemia and oxidative stress in alloxan induced
type I diabetic rat model. Experimental and Toxicologic Pathology 64
(5): 441-448.
- Gosetti F, Chiuminatto U, Martinotti S, Bolfi B, Ranzato E, et al.
(2016) Characterization of the volatile and nonvolatile fractions of
heartwood aqueous extract from Pterocarpus marsupium and evaluation
of its cytotoxicity against cancer cell lines. Planta Medica, 82(14):
1295–1301.
- Chakraborty P, Saraswat G, Kabir SN (2014) α-Dihydroxychalcone-glycoside
(α-DHC) isolated from the heartwood of Pterocarpus marsupium
inhibits LPS induced MAPK activation and up regulates HO-1 expression
in murine RAW 264.7 macrophage. Toxicol Appl Pharmacol
277(1): 95-107.
- Chakraborty A, Gupta N, Ghosh K, Roy P (2010) In vitro evaluation of
the cytotoxic, anti-proliferative and anti-oxidant properties of pterostilbene
isolated from Pterocarpus marsupium. Toxicology in vitro
24(4): 1215-1228.
- Hugar AL, Kanjikar AP, Londonkar RL (2017) A novel potential reproductive
effects of Pterocarpus marsupium Methanolic extract on testosterone
propionate induced polycystic ovary syndrome in female albino
rats. Endocr Metab Immune Disord Drug Targets 17(4): 317-323.
- Xu Y, Zhao Y, Sui Y, Lei X (2018) Protective effect of Pterocarpus marsupium
bark extracts against cataract through the inhibition of aldose
reductase activity in streptozotocin-induced diabetic male albino rats.
3 Biotech 8(4): 188.
- Mathew MM, Han NV, Murugesan A, Raj EA, Prashanth KG (2015)
Evaluation of the protective effect of Pterocarpus marsupium on acetic
acid-induced ulcerative colitis in rats. Inflammopharmacology 23(4):
195-201.
- Hougee S, Faber J, Sanders A, De Jong RB (2005) Selective COX-2
inhibition by a Pterocarpus marsupium extract characterized by
pterostilbene, and its activity in healthy human volunteers. Planta Med
71: 387-392.
- Bose SN, Sepaha GC (1956) Clinical observations on the antidiabetic
properties of Pterocarpus marsupium and Eugenia jambolana. Ind J
Med Assoc 27(11): 388-391.
- Jahromi MF, Ray AB, Chansouria JPN (1993) Antihyperlipidemic effect
of flavonoids from Pterocarpus marsupium. J Nat Prod 56 (7): 989-994.
- Manickam M, Ramanathan M, Farboodniay Jahromi MA, Chansouria
JPN, Ray AB (1997) Antihyperglycemic activity of phenolics from Pterocarpus
marsupium. J Nat Prod 60 (6): 609-610.
- Devipriya D, S Gowri, TR Nideesh (2007) Hepatoprotective effect
of Pterocarpus marsupium against carbon tetrachloride induced damage
in albino rats. Anc Sci Life 27(1): 19-25.
- Mohire NC, Salunkhe VR, Bhise SB, Yadav AV (2007) Cardiotonic activity
of aqueous extract of heartwood of Pterocarpus marsupium 45 (6):
532-537.
- Karanjit N, Shrestha UK, Ranjitkar RR (2008) A study on hypoglycemic
properties of Pterocarpus marsupium Roxb. Bullet Dept Plant Res 30:
97-101.
- Badkhane Y, Yadav AS, Sharma AK, Raghuwanshi DK, Uikey SK, et al.
(2010) Pterocarpus marsupium Roxb-Biological activities and medicinal
properties. Int J Adv Pharm Sci 1 (4).
- Patil UH, Dattatraya KG (2011) Pterocarpus marsupium: a valuable
medicinal plant in diabetes management. Int J App Bio Pharm Tech 2:
6-13.
- Waghmare AS, Waghmare PD, Grampurohit ND, Gadhave MV (2012)
Free radical scavenging activity of methanolic and aqueous extract
of Pterocarpus marsupium heartwood by DPPH method. J Sci Res
Phar 1: 89-91.
- Rizvi SI, Mishra N (2013) Traditional Indian medicines used for the
management of diabetes mellitus. J Diabetes Res: 712092.
- Khan MY, Aziz I, Bihari B, Kumar H, Roy M (2014) A review- Phytomedicines
used in treatment of diabetes. Diabetes 101: 126.
- Hilal A, Kalyanaraman R (2015) Pharmacology of Pterocarpus marsupium
Roxb. Med Plant Res 5: 1–6.
- Pradhan S, Sahu SK, Panda SK, Mishra SS, Chinara PK (2017) Hypoglycaemic
effect of Pterocarpus marsupium. Journal of the Anatomical Society
of India 66: S42.
- Singh P, Bajpai V, Gupta A, Gaikwad AN, Maurya R, et al. (2019) Identification
and quantification of secondary metabolites of Pterocarpus
marsupium by LC–MS techniques and its in-vitro lipid lowering activity.
Industrial Crop Products 127: 26-35.
- Haranath PS, Ranganatha Rao K, Anjaneyulu CR, Ramanathan JD
(1958) Studies on the hypoglycemic and pharmacological actions of
some stilbenes. Indian J Med Sci 12: 85-89.
- Mitra J, T Joshi (1982) An isoflavone glycoside from the heartwood
of Pterocarpus marsupium. Phytochemistry 21(9): 2429-2430.
- Adinarayana D, Syamasundar KV (1982) A new sesquiterpene alcohol
from Pterocarpus marsupium. Phytochemistry 21(5): 1083-1085.
- Chakravarthy BK, Gode KD (1985) Isolation of (-)-Epicatechin
from Pterocarpus marsupium and its Pharmacological Actions. Planta
Med 51(1): 56-59.
- Tripathi J, Joshi T (1988) Phytochemical investigation of roots of Pterocarpus
marsupium. Isolation and structural studies of two new flavanone
glycosides. Z Naturforsch C 43(3-4): 184-186.
- Mohan P, Joshi T (1989) Two aurone glycosides from the flowers
of Pterocarpus marsupium. Phytochemistry 28(4): 1287-1288.
- Jain SC, Sharma SK, Kumar R, Rajwanshi VK, Babu BR (1997) A homoisoflavanone
from Pterocarpus marsupium. Phytochemistry 44(1): 765-
766.
- Mathew J, Subba Rao AV (1983) Carpusin: a novel 2-hydroxy-2-benzylcoumaranone
from Pterocarpus marsupium. Phytochemistry 22(3):
794-795.
- Yadav RK, Singh RK (1998) 6-hydroxy-3,5,7,4′-tetramethoxyflavone
6-rhamnoside from roots of Pterocarpus marsupium. Phytochemistry
48(7): 1259-1261.
- Handa SS, Singh R, Maurya R, Satti NK, Suri KA, et al. (2000) Pterocarposide,
an isoaurone C-glucoside from Pterocarpus marsupium. Tetrahedron
Letters 41: 1579-1581.
- Maurya R, Singh R, Deepak M, Handa SS, Yadav PP, et al. (2004) Constituents
of Pterocarpus marsupium: an ayurvedic crude drug. Phytochemistry
65(7): 915-920.
- Anandharajan R, Pathmanathan K, Shankernarayanan NP, Vishwakarma
RA, Balakrishnan A (2005) Upregulation of Glut-4 and PPAR gamma
by an isoflavone from Pterocarpus marsupium on L6 myotubes: a
possible mechanism of action. J Ethnopharmacol 97(2): 253-260.
- Wu SF, Hwang TL, Chen SL, Wu CC, Ohkoshi E, et al. (2011) Bioactive
components from the heartwood of Pterocarpus santalinus. Bioorganic
and Medicinal Chemistry Letters 21 (18): 5630-5632.
- Thara KM, Zuhara F, Raji TK (2013) Inhibitory and synergistic effect
of Pterocarpus marsupium extracts on clinical and standards strains of
microorganisms and its biochemical analysis. Indo Am J Pharm Res 3:
5583-5596.
- Joshi KR, Devkota HP, Yahara S (2014) Bijayasaline: a new C-glucosyl-
alpha-hydroxy dihydrochalcone from the heartwood of Bijayasal
(Pterocarpus marsupium). Nat Prod Commun 9(6): 821-822.
- Majeed M, Bani S, Natarajan S, Pandey A (2017) Evaluation of 90-day
repeated dose oral toxicity and reproductive/developmental toxicity
of 3’-hydroxypterostilbene in experimental animals. PLoS One 12(3):
e0172770.

