Ethnopharmacological Inspections of Organic Extract of Oroxylum indicum in Rat Models: A Promising Natural Gift

The stem bark of Oroxylum indicum (O. indicum) was aimed at testing for anti-inflammatory, antiulcerative, antihyperglycemic, and antidyslipidemic activities. Liver enzyme concentration (SGPT, SGOT) had also been assessed. After being extracted in organic solvent, 3 distinct doses, 100, 200, and 400 mg/kg b.w. (p.o.), were used. For edema formation 0.1 ml carrageenan at a dose of 1% w/v was injected into paw of left hind. It showed a fall of edemas 37.50%, 48.34%, and 55.83% while used doses were 100, 200, and 400 mg/kg b.w. (p.o.) individually. The EtOH extract of O. indicum (50%) and its fractions PET, CLF, EtOAc, and nBUT were studied against ethanol-induced gastric mucosal damage. Only PET and n-BuOH exhibited the highest percentage of protection and were 96% and 99%, respectively, persuaded by ethanol. In OGTT glibenclamide revealed reduction of glucose level to 7.55 ± 0.22 mmol/L from 10.57 ± 0.32 mmol/L after 30 minutes. Antihyperglycemic activities were assessed for 8- and 12-week duration in diabetic rats. Glibenclamide reduced glucose level from 33.50±0.31 to 7.90±0.19 mmol/L in 12 weeks. In 12 and 8 weeks, combination therapy lowered blood glucose level to a normal extent by 79% and 61% individually. In antidyslipidemic activities after 12-week treatment, it revealed simvastatin; MEOI (400 mg/kg b.w.) and combination of both reduced TC level by 44%, 28%, and 48% consequently followed by TG and LDL. In 8-week treatment, HDL levels were increased by 34%, 13%, and 36%, and in 12 weeks increased by 36%, 8%, and 38% consequently. Liver enzyme concentration after 12 weeks of treatment with glibenclamide, 400 mg/kg b.w. (p.o.) of MEOI and combination of both, exhibited the fact that concentration of SGPT showed downturn by 43.23%, 8.01%, and 54.86% and SGOT by 42.40%, 5.31%, and 44.85%. This study remarked that O. indicum has anti-inflammatory, antiulcer, antidiabetic, and antidyslipidemic potentials but has no ameliorative effect on liver enzyme.


Introduction
The trumpet tree Oroxylum indicum (O. indicum) is found in the tropical region of South East Asian counties like India, Japan, China, Sri Lanka, Malaysia, and Bangladesh [1]. This magnificent plant has many names like Broken Bones, Midnight Horror, Sonapatha, Dashmula, and Shyonaka. This tree is immensely valued in India for its various ayurvedic preparations [2]. It is used as key ingredients of mostly used ayurvedic preparation "Dasamula;" it means ten roots. The whole plant is used as a utilizable part for medicinal value [3]. In folk medicine practices O. indicum has the significance as being an astringent, carminative, blood purifier, tonic diuretic, and laxative, as well as other problems like stomach complaints such as diarrhea, dysentery, and allergic dermatitis [4]. The plant parts, especially seed, ripen fruits, both stem 2 Evidence-Based Complementary and Alternative Medicine and root bark, and leaves, are cherished for various ayurvedic formulations such as Amritarishta, Dantyadyarista, Narayana Taila, Dhanvantara Ghrita, Brahma Rasayana, and Chyawanprash Awaleha [5]. Those ayurvedic preparations are used for inflammation, ulcer, cancer, diarrhea, fever, jaundice, arthritis, and oxidative stress. But all ethnomedical uses of this plant are not experimentally proved by modern technology and research experiments.
Various research works had been conducted for the screening of toxicological studies of the whole part of O. indicum [49][50][51][52][53] and it was observed that dose of this plant (both aqueous and organic one) extract was used in a range from 10 mg/kg b.w. (p.o.) to 5000 mg/kg b.w. (p.o.) considered safe [16,24,54,55]. But it was found that nitrosated ethanolic extract of the bark of O. indicum at a dose of 2000 mg/kg b.w. was genotoxic and mutagenic and toxicity increases on a dose-dependent manner up to 11 folds [52]. Experimental procedure confirmed that O. indicum stem bark extracts showed nonmutagenic, noncytotoxic, and nongenotoxic effects and toxicity information is not reported in any of scientific experiments after studying and comparing its safety profile with that of other plants [56].
After an extensive literature search, this study was aimed at investigating anti-inflammatory, antiulcer, antidiabetic, antihyperlipidemic, and liver enzyme (SGPT and SGOT) activities of stem bark of O. indicum.

Materials and Methods
. . Plant Collection and Processing. For the current investigation, the fresh and raw stem barks of O. indicum were collected during the months of January-February 2017 and authentication was identified by the National Herbarium with accession number DACB-43471. The stem barks were chopped followed by washing and drying at ambient temperature for 72 hours. To obtain powder drying, grinding and sieving of the dried portion were followed by weighing using an analytical balance.
. . Preparation of Crude Methanolic Extract. To prepare crude extract 150 g powdered material was soaked in methanol and the amount of methanol was 900 ml. The round amber color bottle was tightly sealed, kept for a total of 20 days accompanied by occasional shaking and stirring. By using Whatman filter paper filtration was carried. By using rotary evaporator at 7-8 rpm and with a temperature of 68 ∘ C crude methanolic extract of O. indicum (MEOI) was collected after evaporation of methanol. This generated extract was used for anti-inflammatory, antidiabetic, antihyperlipidemic, and liver enzyme (SGPT and SGOT) activities.

. . Preparation of Crude Ethanolic Extract and Its Fractions
for Antiulcer Activities. For the preparation of crude extract dried stem bark was weighed for 150 g and grinded to 60 mesh size. Then the grinded materials were dissolved in 2 L ethanol (50% ethanol in water) for twenty days in a conical flask accompanied by occasional shaking and stirring. This was followed by filtration and the filtrate was dried using rotary evaporator (yield 18.34%). The extracted material was then extracted by petroleum ether (PET) followed by drying (yield 0.35% w/w). The residual material was then air-dried and liquid ammonia solution was used to moisten the dried material. The residual material again was extracted with chloroform (CLF) followed by drying (yield 1.90% w/w). Again the remaining unextracted material was then extracted with n-butanol (n-BuOH) and ethyl acetate (EtOAc) sequentially to obtain n-BuOH (yield 2.2% w/w) and EtOAc (yield 2.9% w/w) fractions. The dried fractions were conserved in air tight humidity protected borosilicate glass container.
. . Collection of Test Animals. A number of 400 test animals were purchased from the Research Institute International Centre for Diarrhoeal Disease Research, Bangladesh (ICDDR,B). Both Swiss Albino and Long Evans rats aged 4-6 weeks, having the weight of 200 to 220 g, were subjected for anti-inflammatory, antiulcerative, antidiabetic, and antidyslipidemic test. Liver enzyme concentration had also been tested. Groupings were done according to need for each test and protocols among with time duration. Rats were kept at ambient temperature (25-28 ∘ C) and maintained at dark/light cycles followed by acclimation of necessary duration. The standard pellet was purchased from ICDDR,B for their diet and additional fat-enriched diet supplied. Both sex rats were used but kept separately for the purpose of avoiding breeding. Animal ethics had been strictly maintained and handled them in the most human way. Coprophagy carefully was prevented. The animals groupings were done randomly. All reagents were prepared instantly. Within the whole study period, it was ensured that rats were healthy and playful. The cervical dislocation procedure was used to sacrifice all rats. Animals after sacrifice dumped according to rule [57][58][59][60]. Animal ethical committee approved the whole protocol.
. . Drugs and Chemicals for Anti-Inflammatory Activity. All solvents and reagents including -carrageenan were procured from Sigma-Aldrich, USA. Ibuprofen was a generous gift of Eskayef Pharmaceutical Company Ltd., Bangladesh.
. . Grouping of Animals. Swiss Albino rats aged 4-6 weeks having the weight of 180 to 200 g were subjected for antiinflammatory study. Each group contained 6 rats. The animals were kept whole day fasting and only allowed drinking water before the experiment started and coprophagy was carefully prevented.
. . Anti-Inflammatory Activity. To measure anti-inflammatory activity the same procedure followed MEOI suggested by Winter et al. [61], by using carrageenan as an edematogenic agent after some modification. Six rats were in each group and a total of six groups were made. Group I was considered as control, treated with only 0.9% saline with 2-3 drops of tween 80. Group II was given 0.9% saline and 0.1 ml 1% carrageenan. Group III was treated with ibuprofen (10 mg/kg b.w.) as a reference drug. Group IV, group V, and group VI were treated with crude extract and doses were 100, 200, and 400 mg/kg b.w. individually. After one hour, each rat was injected 1% carrageenan dissolved in a saline solution into the right hind paw. The paw edema volume was computed every hour using slide calipers and the left hind paw was considered as a reference of the noninflamed paw for comparison. The following formula was used for calculation of percentage inhibition of paw edema: Vc denotes the average paw volume of control animal and Vt represents the average paw volume of treated animal.
. . Histological Evaluation. To evaluate histopathological examination, rat paws were collected 6 hours after the induction with an inflammatory agent (carrageenan). The tissue slices (5 m thick) were processed for histological evaluation of inflamed paw 10% by keeping it within formalin buffer at 4 ∘ C. After that histopathology examination was done from the Histopathology Unit of Popular Hospital, Dhaka, Bangladesh.
. . Drugs and Chemicals for Antiulcer Activity. Omeprazole was collected from the Eskayef Pharmaceutical Company Ltd., Bangladesh. Solvents and reagents were confirmed to be of analytical grade. Oral administration of omeprazole was done by dissolving it in dimethyl sulfoxide (DMSO).
. . Grouping of Animals. Long Evans rats aged 4-6 weeks having the weight of 200 to 220 g were subjected for antiulcerative study. Each group contained 6 rats. The animals were kept fasting 24 hours before the experiment started and coprophagy was carefully prevented.
. . Antiulcer Activity. Pretreatment procedure was followed for examining mucosal damage in gastric cell lining. To do so, standard drug omeprazole and all distinguished doses of aforesaid test samples of O. indicum were administered. Ulcer model was induced by ethanol acid in a fixed dose measured in each rat except for normal control. The dose was 25 ml/kg of 0.3M hydrochloric acid in 60% ethanol [62]. Waiting till 90 minutes after persuasion of ulcer all rats were sacrificed and stomachs were collected and instantly excised along the larger curvature and washed. The magnifying lens was used to examine ulcers in gastric mucosa and scoring of ulcer calculated [63]. Crude EtOH of stem bark of O. indicum and its different fractions, namely, PET, CLF, EtOAc, and nBUT, was observed against damage of gastric mucosa. The methanol extract and its different fractions were used for finding out the ulcerative profile. Ulcer index was calculated by using the mean ulcer score. The ulcer protection percentage was estimated by using the following equation: U c denotes the average ulcer index of control animal and U t represents the average ulcer index of treated animal. Lesions were assessed by unbiased neutral observers using a 7 binocular magnifier. Grouping of rats for antiulcerative activities was done as normal control, ethanol control, 100, 200, and 400 mg/kg b.w. per oral along with a dose of ulcer induction by ethanol acid.
. . Drugs and Chemicals for Antidiabetic, Antihyperlipidemic, and Liver Enzyme Activities. The drug glibenclamide and simvastatin both were obtained from Eskayef Pharmaceutical Company Ltd., Bangladesh. Total cholesterol TC, TG, LDL, HDL, SGPT, and SGOT kits and Alloxan were brought from Sigma-Aldrich, USA.
. . Grouping of Animals. A total of 84 Long Evans male rats were grouped for both glucose tolerance test and antidiabetic tests. In glucose tolerance test a total of 24 rats were used in four different groups after time intervals 0, 0.5, 1, and 2 hours, respectively. Other 60 rats were divided into five individual groups. Group I was considered as normal control. Group II was diabetic control. Group III was treated with standard glibenclamide. Group IV was treated with 400 mg/kg b.w. p.o. MEOI. Group V was treated with a combination of glibenclamide and 400 mg/kg b.w. p.o. of MEOI. The same grouping was repeated and implemented in case of finding hypolipidemic activities by simvastatin and experimental crude samples. . . Collection of Blood Serum and Liver. After finishing 8week and 12-week treatment the rats were anesthetized with phenobarbital sodium. With heparinized syringe, an average of 4 ml blood was collected by cutting the thoracic artery and the collected sample was centrifuged at 3000 rpm for 20 minutes and serum was collected for the test.
. . Oral Glucose Tolerance Test. The oral glucose tolerance test (OGTT) was performed by the Vigneaud et al. 's [53] method. After overnight fasting, 1.5 gm/kg per oral glucose was administered and glucose level estimated in blood at 0, 0.5, 1, and 2 hours' interval. Glibenclamide, a blood glucose lowering drug, was administered (at a dose of 1.2mg/70kg b.w. per oral) two hours prior to glucose intake.

. . Antihyperglycemic and Antihyperlipidemic Activities.
Five different groups were prepared for testing the antihyperglycemic effect. A total of 12 hours of starvation were maintained for experimental rats. All the rats were tested for a baseline glucose level using a glucometer. The first group for the normal group received no drug, the second group was selected for the diabetic control group, and the third group stands for glibenclamide received a dose of 1.2 mg/70kg b.w. The fourth group stands for methanolic extract of O. indicum at a dose of 400 mg/kg b.w., p.o. The fifth group received the combination of drugs (glibenclamide and MEOI) mentioned earlier.
For hypolipidemic activities, the same grouping and procedure were followed with a dose of 10 mg/70kg b.w. and combination therapy received the 5mg/70kg b.w., the dose of simvastatin, and 400 mg/kg b.w., p.o., dose of O. indicum.
. . . Eight-and Twelve-Week Repeated Dose Treatment of Glibenclamide, MEOI, and Combination of Both. For the determination of blood glucose level in the diabetic rat model induced by alloxan, 8-and 12-week treatment protocols were conducted. According to this procedure glibenclamide, MEOI, and combination of both (glibenclamide and MEOI) were administered daily and after completion of treatment glucose level was detected by glucometer.
. . . Eight-and Twelve-Week Repeated Dose Treatment of Simvastatin for Hyperlipidemia, SGPT, and SGOT Levels. Collected serum from thoracic artery was subjected to various lipid levels. Level of TC, TG, LDL, and HDL in serum and level of SGPT and SGOT were also determined by diagnostic kit manufactured by Sigma-Aldrich, USA. For performing these tests the International Federation of Clinical Chemistry (IFCC) standard was followed [64].
. . Statistical Analysis. To represent glucose level and lipid and liver enzyme level all comparable results were expressed by mean±SEM. For this purpose GraphPad Prism software was used. Data were analyzed by ANOVA followed by Dunnett's multiple comparison test, to find out the significance level of values.

Results
. . Evaluation of Anti-Inflammatory Activity. After treatment, it was observed that reference standard drug ibuprofen (20 mg/kg b.w., p.o.) and all different doses of methanolic extract (100,200, and 400 mg/kg b.w., p.o.) revealed considerable depletion in paw thickness in a total duration period of six hours (Table 1). Compared to carrageenan control it was seen that all different doses of extract showed considerable anti-inflammatory activity which was significant (p< 0.01). After completion of study in 6 hours it was noticed that ibuprofen (20 mg/kg b.w.) at the end of the study (20 mg/kg b.w.) spotted 53.33% of inhibition and all methanolic extracts (100,200, and 400 mg/kg b.w.) decreased edema in mice paw by 37.50%, 48.34%, and 55.83% individually.
In naked eyes, it was observed that, after induction of carrageenan, edema formation was noticeably observable characterized by redness and swelling in all six groups, . . Histopathology of Tissue Obtained from Paw. After histopathological examination (Figure 1) it was observed that as reference standard drug ibuprofen, the highest dose extract of O. indicum (400 mg/kg b.w.), put down the cell infiltration and suppressed inflammation. But more tissue level analysis needs to explain with extract mechanism how the extract of MIOE works. The photomicrograph from paw tissue of normal control group rat showed only minimal  inflammatory cells infiltration (Figure 1(a)) whereas the photomicrograph from paw tissue of carrageenan control group showed numerous infiltrations of inflammatory cells (arrow) (Figure 1(b)). The photomicrograph from paw tissue of the ibuprofen treated group showed minimal inflammatory cells (Figure 1(c)). On the other hand, the photomicrograph from methanolic extract treated groups (100 and 200 mg/kg b.w.) showed a moderate number of inflammatory cells (Figures  1(d) and 1(e), resp.). However, the photomicrograph from the highest dose extract of O. indicum (400 mg/kg b.w.) put down the cell infiltration and suppressed inflammation (Figure 1(f)).
. . Evaluation of Antiulcer Activity. For the study of gastric mucosal damage crude extract in ethanol and different fractions, namely, PET, CLF, EtOAc, and nBUT, was monitored. One hour after inducing an ulcer, animals were sacrificed. The stomachs were excised and were opened over the greater curvature and rinsed with saline solution (0.9%) to remove the blood clots. Thereafter, each gastric sample was placed on a slide. The gastric damage area was firstly observed by Tripod magnifier (10 × magnification) for primary observation before being subjected for histopathological studies. Close monitoring revealed that ulcer formation in the gastric layer was potentiated by acute to subchronic gastritis. This was characterized by hemorrhagic lesions followed by damage of mucosal capillaries, increased permeability, and aggregation of platelets and clot formation. Stomachs obtained from the normal control group were healthy and viable and no clot formation occurred under cell line. But in ethanol control group stomachs were perforated, red marked, and were frequently identified due to hemorrhagic lesions and capillary rupture. For treatment with doses of 100 and 200 mg/kg b.w./day both group stomachs were examined with gastric lesion and mildly notable blood clot formation due to the injury of cell line layer. But in the stomachs treated with 400 mg/kg b.w./day dose of O. idcicum there were no noticeable perforation, blood clot formation, and cell damage. Stomachs were healthy and in fine fettle compared to the control group. It was showed ( Table 2) that control group indicated ulcer index 7.04±0.112 with zero percentage of inhibition. But nBUT and PET showed 0.07±0.007 and 0.27±0.011 ulcer    (Table 4). But 400 mg/kg b.w., p.o. dose of MEOI suppressed glucose level in blood only by 26% but not remarkably. Combination therapy, on the other hand, reduced blood glucose level to a normal extent by 61%. Glibenclamide alone indicated notable (p< . ) downturn in glucose level from 33.5 ± 0.31 to 7.9 ± 0.19 mmol/L after completing 12 weeks of treatment in diabetic rats (Table 5). At the dose of 400 mg/kg b.w., p.o. of MEOI there was decrease in blood glucose level by 37% whereas glibenclamide was lessened to 77% in blood glucose level which was noteworthy. Combination therapy, on the other hand, lowered blood glucose level to a normal extent by 79%. Combination dose (glibenclamide+ 400 mg/kg b.w. of MEOI) showed nearly the same result as glibenclamide did and did not exhibit any additive or synergistic effect in both 12-and 8-week treatment protocols.

. . . Effects on Lipid Profile in Rats in -and -Week Treatment by Simvastatin, MEOI, and Combination erapy.
Tables 6, 7, 8, and 9 demonstrated lipid-lowering ability of simvastatin, MEOI, and combination of both drugs after repeated dose treatment for 8 and 12 weeks on the lipid profile in diabetic rats model induced by alloxan. After 8 weeks of treatment, it was revealed that simvastatin, MEOI, and combination of both drugs reduced total cholesterol level by 40%, 22%, and 44% (Table 6), respectively, but in 12-week treatment total cholesterol level was reduced by 44%, 28%, and 48% after applying the same dose of simvastatin, MEOI, and combination of both drugs. In 8-and 12-week treatment Evidence-Based Complementary and Alternative Medicine 7     protocol triglyceride levels were reduced by 32%, 15%, and 35% and 32%, 17%, and 36%, respectively (Table 7). LDLcholesterol levels were reduced by 28%, 4%, and 31% in 8week treatment protocol while in 12-week treatment protocol levels were reduced by 28%, 5%, and 33% (Table 8). In 8-week treatment protocol both HDL levels were increased by 34%, 13%, and 36% and in 12 weeks increased by 36%, 8%, and 38% consequently (

Discussion
Phytoconstituents are the backbone for exerting copious therapeutic actions and aid as a blueprint for the discovery and development of new pharmaceuticals [65][66][67]. In this study, anti-inflammatory, antiulcer, antidiabetic, antihyperlipidemic, and liver enzyme activities of stem bark of O. indicum were investigated.    In case of anti-inflammatory activities, the edema in the right paws could be segmented into the first phase followed by the second phase [68,69]. In phase one, edema formation occurred instantaneously after carrageenan injection. The first phase counted for two hours approximately. Phase two counted for two to up to six hours and larger edema formation occur characterized by redness and swelling. This inflammatory action was due to various inflammatory chemicals like prostaglandin, prostacyclin, and leukotriene followed by the pathway COX 2 mechanism [22,[70][71][72][73]. Noticeably Figure 1(a) group was distilled water treated paw with no carrageenan injection which demonstrated damaged tissue and was conserved for the identification of dermal collagen and leukocytes. Figure 1(b) indicated swelling and redness after carrageenan injection induction due to diapedesis and chemotaxis by inflammatory cells including white blood cells and red blood cells. Figure 1(c) denoted treatment with ibuprofen (20 mg/kg b.w.) with slight inflammatory cells appearance. Figures 1(d) and 1(e) both indicated that methanolic extract with doses of 100 and 200 mg/kg b.w. showed mild to moderate cell infiltration. Followed by treatment with the dose of 400 mg/kg b.w. in Figure 1(f) it was observed that cells' infiltration was nearly abolished. The extract of MEOI showed a considerable antiinflammatory effect. Also, the histopathological examination of paws revealed that methanolic extract of O. indicum reduced aggregation of inflammatory cells. All studies support previous experiment with different parts (seed) of the same plant. All these observations in different groups showed similarities with previous studies [74][75][76][77][78][79][80][81][82][83].
In case of screening of antiulcer property, ethanol was used to produce mucosal damage in the stomach layer.
Extract of O. indicum (with the dose 400 mg/kg b.w., p.o.) exhibited a substantial downturn for reduction of gastric ulceration. Omeprazole was used as a standard drug and after treatment procedure it was observed that standard omeprazole, PET, and nBUT showed a considerable reduction in ulceration. The extract was used at a dose of 400 mg/kg b.w. and among all fractions the PET (96%) and nBUT (99%) fractions manifested sharp reticence of gastric lesions against mucosal damage induced by ethanol acid. The comparison was done with reference standard drug omeprazole and the ulcer model after treatment with both active fractions and omeprazole showed dramatic gastric mucosal damage conservation. This study also supports previously done experimental studies [46,[84][85][86][87][88][89][90][91][92][93].
In case of antidiabetic activity, glibenclamide is considered as good glucose level lowering drug and exhibited significance. In both treatment procedures, namely, 8 weeks and 12 weeks, individual dose of extract of O. indicum revealed reduction of blood glucose level but it was not noteworthy on the contrary that combination dose (for both 8 and 12 weeks) was able to decrease glucose level in a significant extent. A number of flavonoids compounds had been separated and identified especially from bark (both stem and root) leaves and seeds. Two chemicals, namely, oroxylin A (baicalein-7-oglucoside) and oroxin A, have antidiabetic potentials [46,47]. These phenomena support the previous experiment as among all constituents oroxylin A and oroxin A both have insulin resistance potentials and have capability of inhibiting glucosidase [32,46,47]. It was seen that extracted constituent revealed more activity than the crude extract. In both timeand dose-dependent treatment protocols it was monitored that long-term (12 weeks) treatment showed a drop of glucose level compared to short-term (8 weeks) treatment. In both cases only combination therapy showed significance and was supported by preceding studies [46,47,[94][95][96][97][98][99][100][101].
For the assessment of hypolipidemic activity, the extract alone (400mg/kg b.w., p.o.) failed to decline TC, TG, and LDL level by remarkable level. But a mild drop of lipid level occurred in each case. Only in case of 12-week treatment combination therapy showed significance in lowering lipid level. In case of HDL level elevation combination therapy indicated a considerable upward trend. This study also supports the previous experiment as simvastatin was treated as a very potential lipid-lowering drug and coincided with prior studies [102][103][104][105][106]. To identify the level enzymes (both SGPT and SGOT) both treatment protocols failed to decrease the level of specific enzyme level to a noteworthy extent and exhibited similarities with past studies [107][108][109][110][111][112][113] but revealed satisfactory decline. Liver enzymes SGPT and SGOT are considered as surrogate markers of diabetes mellitus complication. This study also showed that stem bark alone has no significant effect on liver enzyme concentration. For liver enzyme concentration assessment, neither individual dose of MEOI nor combination did show any significant reduction. Cases of TC, TG, LDL, and HDL level except simvastatin which was used as a standard drug and combination of simvastatin and 400 mg/kg b.w. MEOI showed significance but the dose of extract at 400mg/kg b.w alone did not show any significance.

Conclusion
Extract of O. indicum exhibited potent and remarkable anti-inflammatory and antiulcer activities. On the other hand, it showed moderate antidiabetic and antidyslipidemic properties and liver enzymes' concentration lowering effects. However, the mechanisms behind all those effects are still not in daylight. Therefore, further experiments should be carried out for the purpose of the phytoconstituents and expected mechanisms that are subjected and interrelated to the constituents to exhibit various effects in both in vivo and in vitro experimental models. Standard error mean TNF : T umornecrosisfactoralpha IL6: Interleukin 6 p38MAPK: Mitogen-activated protein kinase p38.

Data Availability
The experimental data obtained from various rat models used to support the findings of this study are available from the corresponding author upon request.

Ethical Approval
All experimental protocols in this study involved animals and all tests have been performed according to ethical standards and guidelines provided and instructed by Biomedical Research Centre, University of Dhaka, Bangladesh, with reference No. BMRC/EC/2017-18/386.