Effect of 2-Hydroxy-4-Methoxy Benzoic Acid from the Roots of Hemidesmus indicus on Streptozotocin-induced Diabetic Rats

1. Nostro A, Germano MP, DAngelo V, Marino A, Canntelli MA. Extraction methods and bioautography for evaluation of medicinal plant antimicrobial activity. Lett Appl Microbiol 2000;30:379-84. 2. Hammer KA, Carson CF, Riley TV. Antimicrobial activity of essential oil and other plant extracts. J App Microbiol 1999;86:985-90. 3. Veale DJ, Furman KI, Oliver DW. South African traditional herbal medicines used during pregnancy and childbirth. J Ethnopharmacol 1992;36:185-91. 4. Jain A, Basal E. Inhibition of Propionibacterium acnes-induced mediators of inß ammation by Indian herbs. Phytomedicine 2003;10:348. 5. Mousa O, Vuorela P, Kiviranta J, Wahab SA, Hiltunen R, Vuorela H. Bioactivity of certain Egyptain Ficus species. J Ethanopharmacol 1994;41:71-6. 6. Jung M, Park M, Lee HC, Kang YH, Kang ES, Kim SK. Antidiabetic agents from medicinal plants. Curr Med Chem 2006;13:1203-18. 7. Perez C, Paul M, Bazerque P. Antibiotic assay by agar-well diffusion method. Acta Biol Med Exp 1990;15:113-15. 8. Attata RF, Sani A, Ajewole SM. Effect of stem of bark extracts of Enantia chloranta on some clinical isolates. Biokemistri 2003;15:84-92. 9. Harbone JB, Phytochemical Methods. 2nd ed. London: Chapman and Hall; 1984.p.55-70. 10. Hiremath SP, Rudresh K, Badani S. Antimicrobial activity of various extracts of Striga sulphurea and Hemidesmus indicus. Indian J Pharm Sci 1997;59:145-47. 11. Austin A, Jegadeesan M, Gowrishankar R. Antimicrobial activity of Hemidesmus indicus var.indicus R.Br. against human isolates of Helicobacter pylori. Nat Prod Sci 2003;9:1-3. 12. Das S, Devaraj SN. Antienterobacterial activity of Hemidesmus indicus R. Br. root extract. Phytother Res 2006;20:416-21. 13. Das S, Prakash R, Devaraj SN. Antidiarrhoeal effects of methanolic root extract of Hemidesmus indicus (Indian sarsaparilla), an in vitro and in vivo study. Indian J Exp Biol 2006;41:363-66. 14. Proestos C, Chorianooulos N, Nychas GJ, Komaitis M. RP-HPLC analysis of the phenolic compounds of plant extracts: Investigation of their antioxidant capacity and antimicrobial activity. J Agr Food Chem 2005;53:1190-95. 15. Chacha M, Bojase-Moleta G, Majinda RR. Antimirobial and radical scavenging flavonoids from the stem wood of Erythrina latissima. Phytochem 2005;66:99-104. 16. Slobodnikov L, Kostalova D, Labudova D, Kotulova D, Kettmann V. Antimicrobial activity of Mahonia aquifolium crude extract and its major isolated alkaloids. Phytother Res 2004;18:674-76. 17. Chung KT, Wong TY, Wei CI, Hung YW, Lin Y. Tannins and human health: A review. Crit Rev Food Sci Nutr 1998;38:421-64. 18. Mandal P, Sinha Babu SP, Mandal NC. Antimicrobial activity of saponins from Acacia auriculiformis. Fitoterpia 2005;76:462-65. 19. Wiesman Z, Chapagain BP. Larvicidal activity of saponins containing extracts and fractions of fruit mesocarp of Balanites aegyptica. Fitoterapia 2006;77:420-4.


September -October 2009
Hemidesmus indicus (Asclepiadaceae) is one of the indigenous Ayurvedic medicinal plants commonly available and widely distributed throughout India.The root bark of this plant has been used as a traditional medicine in the treatment of biliousness, blood diseases, diarrhea, respiratory disorders, skin diseases, syphilis, fever, bronchitis, asthma, eye diseases, epileptic fits in children and also used to treat kidney and urinary disorders, loss of appetite, burning sensation and rheumatism [1] .H. indicus is also employed in traditional medicine for the treatment of gastric ailments [2] .It mainly consists of essential oils and phytosterols such as hemidesmol, hemidesterol and saponins.Isolation of 2-hydroxy-4-methoxy benzoic acid (HMBA) from H. indicus was already reported [3] .It was reported that it exists as white needle-shaped crystals, soluble in water, methanol and chloroform and has a melting point of 155-158° and λ max 260 nm [3] .The presence of a benzene ring, methoxy group and hydroxyl group in the structure of HMBA having the molecular formula of C 8 H 8 O 4 and the molecular weight was calculated as 168 [3] .The concentration of HMBA in the root bark of H. indicus was in the range of 0.03-0.54% [4].It possess potent antiinß ammatory, antipyretic and antioxidant properties [5] .It also neutralizes viper-venom-induced changes in serum phosphatase and transaminase activity in male albino rats and also reduced free radical formation [6] .The compound also has an adjuvant effect and antiserum potentiating activity against viper venom [7] .ACGIH, IARC, NIOSH, NTP and OSHA do not list it for carcinogenicity.The protective effect of H. indicus against rifampicin-and isoniazid induced hepatotoxicity in rats [8] , as well as CCl 4 and paracetamol-induced hepatic damage [9] , is known.Recently we have reported the antidiabetic activity of the aqueous extract of H. indicus in streptozotocin-induced diabetic rats [10] .In the present investigation HMBA was isolated from the roots of H. indicus and tested for antidiabetic and antiperoxidative activity in STZ-induced diabetic rats.
The root of H. indicus, was collected from the Morappur forest area, Dharmapuri District, Tamil Nadu, and authenticated by the forest department, where a voucher specimen (FDSC201) was also submitted.Roots of H. indicus was washed with distilled water, shade dried, powdered and stored in an air-tight container until further use.The protocol used for animal experimentation was approved by the Institution Animal Ethical Committee, (IEAC, VIT University).
The UV spectra of the puriÞ ed fraction were carried out in a Perkin-Elmer Spectrophotometer (Model 5503) in the wavelength region of 200 to 800 nm.Nuclear magnetic resonance spectra ( 13 C and1 H NMR) were measured using DMSO as solvent in 200 MHz.Gas chromatography combined with mass spectrum of the puriÞ ed fraction was recorded using AcqMethod AUTO GCMS.The puriÞ ed fraction was also identified by X-ray crystallographic analysis.The crystal was mounted on a goniometer head and X-ray data were collected using CuKa radiation.The structure was solved using Direct Method procedure using computer programme, SHELX-86 and reÞ ned by SHELXS-93.The Zortep plot of the compound was plotted.The physical characteristics like melting point, boiling point and the solubility of the compound was determined.Based upon the spectroscopic and crystallographic studies, the structure of the active compound was identified.The purity of the isolated compound was conÞ rmed with the standard 2-hydroxy-4-methoxy benzoic acid (HMBA) purchased from the Sigma-Aldrich Chemical Co., USA (Cat # 17,347-9).
Male Wistar rats (150-200g) were purchased from Tamil Nadu Veterinary Animal Science University, Madhawaram, Chennai, and housed under standard husbandry conditions (30±2 o , 60-70% relative humidity and 12 h:12 h day-night cycle) and allowed standard pellet rat feed and water ad libitum.Animals were housed in standard environmental conditions (as per Institutional Animal Ethical Committee norms).Tolbutamide was purchased from Apollo Pharmacy, Vellore, India.
Diabetes was induced experimentally in rats by a single intraperitoneal injection of freshly prepared solution of streptozotocin (STZ, Sigma, St. Louis, USA) at a dose of 35 mg/kg body weight in 0.1 M citrate buffer, pH 4.5.The STZ-treated animals were considered to be diabetic, if the blood glucose values were above 250 mg/dl and stabilized for a period of 7 days and those animals alone were selected for this study.Animals were divided into four groups of six animals each.Group I served as a control; group II had STZ-induced surviving diabetic rats; group III served as a positive control and received a standard hypoglycemic agent, tolbutamide (100 mg/kg) by oral intubation method and group IV diabetic rats treated with the HMBA (500 μg/kg) for 7 weeks by oral intubation method.Blood samples were collected from the tail vein using aseptic precautions at the end of the treatment period in the tube containing potassium oxalate and sodium fluoride for the estimation of plasma glucose by glucose oxidase method [11] , and plasma insulin (Radioimmunoassay kit, Pharmacia, Sweden) [12] .The levels of TBARS in plasma [13] , erythrocytes, erythrocyte membrane and erythrocyte membrane Ca 2+ -ATPase activity [14] were measured.
Statistical analysis was performed using SPSS software package, version 9.05.The values were analyzed by one way analysis of variance (ANOVA) followed by Duncan's multiple range test (DMRT).All the results were expressed as mean ±SD for six rats in each group P<0.001 were considered as statistically signiÞ cant.
The FTIR (KBr) spectrum showed bands at 1650 and 1620 cm -1 for COOH grouping and aromatic moieties.The 13 C NMR spectrum of the compound exhibited signals for eight carbons, of which a quartlet at δ174.2 ppm supported the presence of a COOH group.The remaining three doublets at δ 101.0, 108.1 and 132.4 ppm and three singlets at δ164.6 and 168.8 ppm indicated the presence of a trisubsituted aromatic ring in the molecule. 1H NMR (CDCI 3 ) spectrum displayed, besides the signals for OMe (δ3.86 ppm) and intramolecular hydrogen bonded OH protons (δ 10.59 ppm), two ortho coupled signals at δ 6.51 and 7.86 ppm (J=9 Hz), the former being split further by a meta related proton (with J=2Hz), which in turn resonated as a doublet at δ 6.45 ppm (J=2Hz).The spectral data of the compound showed the m/z at 168, corresponding to the molecular weight and the molecular formula C 8 H 8 O 4 .Based on the spectral data the pure compound was identified as HMBA and the structure was assigned for the compound.The X-ray crystallographic data also confirmed that the compound is HMBA.
The % yield of HMBA obtained was about 2.5% and the purity was 99%.The physical characteristic features of HMBA are given Table 1.The effect of HMBA on plasma glucose, insulin and erythrocyte membrane low affinity Ca 2+ -ATPase activity is given in Table 2. Oral administration of aqueous solution of HMBA significantly (F>0.05;P<0.001) reduced the blood glucose level and increased the level of plasma insulin to near normal level when compared to untreated control rats.In diabetic rats the activity of low afÞ nity Ca 2+ -ATPase was considerably decreased.Oral administration of HMBA increased the activity of low afÞ nity Ca 2+ -ATPase signiÞ cantly (F>0.05;P<0.001) to normal level.The effect of the HMBA on plasma, erythrocytes membrane and erythrocytes lipid peroxidation is given in Table 3.The signiÞ cantly (F>0.05;P<0.001) elevated levels of TBARS in plasma, erythrocytes and erythrocyte membrane of diabetic rats were reduced signiÞ cantly (F>0.05;P<0.001) to near-normal levels upon treatment with HMBA.
In our study, diabetic rats had elevated level of blood glucose and treatment with HMBA and tolbutamide reduced blood glucose level signiÞ cantly, which could be associated with increased secretion of insulin.
For induction of diabetes low concentration of STZ (35 mg/kg) was used and diabetic rats still possess functional islets cells.It was well documented that during diabetes mellitus reactive oxygen species (ROS) were generated and the increased levels of ROS can cause increased lipid peroxidation and there by elevation of lipid peroxidation markers.
In the present study, the elevated levels of TBARS in plasma, erythrocyte and erythrocyte membrane are consistent with earlier reports [15] .Treatment with HMBA and tolbutamide reduced the levels of TBARS to near normal, which could be associated with improved glycemic control.The observed effect of HMBA may be due to its antioxidant activity.
Our report is consistent with the earlier reports that HMBA possess signiÞ cant antioxidant activity [5].
Hyperglycemia can cause glycosylation of proteins and cellular lipid peroxidation, which, in turn, can cause inhibition/reduction in the activity of Ca 2+ -ATPases.This in turn, can affect the intracellular concentration of Ca 2+ , thereby alter the signal transduction pathways, and also affect contractility and excitability and cellular dysfunctions [16] .Diabetic rats had decreased activity of low affinity Ca 2+ -ATPase as a consequence of interaction of glucose with Ca 2+ -ATPase [16] .The activity of low afÞ nity Ca 2+ -ATPase was found to decreased in the erythrocytes of diabetic rats.Increased lipid peroxidation can, in turn, diminish the activity of low afÞ nity Ca 2+ -ATPase in erythrocyte membrane when exposed to a higher glucose concentration-containing medium [16] .Diabetic rats treated with HMBA and tolbutamide showed the reversal of low afÞ nity Ca 2+ -ATPase to near normal level which might be associated with decreased peroxidative damage to erythrocyte membrane phospholipids along with improving glycemic control.Thus HMBA treatment restored low affinity Ca 2+ -ATPase by decreasing lipid peroxidation and also improves glycemic control.Insulin has been reported to have direct effect on regulation of the membrane bound (Ca 2+ +Mg 2+ )-ATPase [17] .Low-affinity Ca 2+ -ATPase is considered to be responsible for the shape  and deformability of the erythrocyte membranes [18] .In our study, diabetic rats showed decreased activity of low affinity Ca 2+ -ATPase and this could be due to insulin deÞ ciency and insulin being the regulator of the enzyme.Treatment with HMAB restored the level of low affinity Ca 2+ -ATPase, which might be associated with insulin secretary effect.The results of this study demonstrate that HMBA exhibits promising antidiabetic activity and also helps to maintain glycemic control by curbing ROS.

TABLE 2 : EFFECT OF HMBA ON PLASMA GLUCOSE, INSULIN LEVELS AND ERYTHROCYTE MEMBRANE CA 2+ -ATPASE ACTIVITY Groups Dose (mg/kg bw/day) Plasma glucose (mg/dL) Plasma insulin (µU/ml) Ca 2+ -ATP ase activity (μ mole Pi/mg protein/h)
Each value is mean±SD for six rats in each group.*Values are statistically signiÞ cant when compared to diabetic control at F>0.05(ANOVA) and P< 0.001 (DMRT).

TABLE 3 : EFFECT OF HMBA ON PLASMA, ERYTHROCYTE AND ERYTHROCYTE MEMBRANE TBARS LEVELS
Each value is mean±SD for six rats in each group.*Valuesare statistically signiÞ cant when compared to diabetic control at F>0.05(ANOVA) and P< 0.001(DMRT).