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In vitro evaluation of the antidiabetic properties of a traditional Sooranam polyherbal ethanolic extract
*Corresponding author: G. Arunachalam, M.Pharm., Ph.D., FIC., PGP College of Pharmaceutical Science and Research Institute, Namakkal, Tamil Nadu, India. arunachalampharm@yahoo.com
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Received: ,
Accepted: ,
How to cite this article: Arunachalam G, Sriram T, Jenifer BG, et al. In vitro evaluation of the antidiabetic properties of a traditional Sooranam polyherbal ethanolic extract. Am J Pharmacother Pharm Sci. 2026:006
Abstract
Objectives:
Diabetes mellitus is a complex metabolic disorder characterized by persistent hyperglycemia due to impaired insulin secretion and insulin resistance, leading to complications such as nephropathy, retinopathy, and neuropathy. Traditional medicinal plants have been extensively used in India for diabetes management due to their rich bioactive profiles and low adverse effects. This study aimed to evaluate the antidiabetic potential of ethanolic Sooranam extracts prepared from 14 medicinal plants collected from Kolli Hills, Tamil Nadu, India.
Materials and Methods:
The polyherbal ethanolic extract was assessed using in vitro antidiabetic assays, including α-amylase inhibition, α-glucosidase inhibition, and glucose uptake enhancement in yeast and muscle cell models.
Results:
The ethanolic extract of Sooranam contained flavonoids, phenolics, tannins, alkaloids, and saponins, indicating strong antidiabetic potential. It showed dose-dependent α-amylase inhibition (10.69–91.56%) with an IC50 of 23.70 µg/mL and α-glucosidase inhibition (7.99–92.67%) comparable to voglibose. The extract also enhanced glucose uptake in yeast cells from 42.8% to 81.7% across increasing concentrations. Overall, the 15PC formulation exhibited multi-target antidiabetic activity through enzyme inhibition and improved glucose utilization.
Conclusion:
The findings indicate that the Sooranam polyherbal ethanolic extract from Kolli Hills possesses promising in vitro antidiabetic activity. Its enzyme inhibitory effects and glucose uptake enhancement support its potential as a natural antidiabetic agent.
Keywords
Antidiabetic Activity
Diabetes mellitus
Ethanol extract
Hyperglycaemia
Medicinal plants
INTRODUCTION
Type II diabetes mellitus stands as a predominant metabolic disorder of contemporary clinical concern.[1] Diabetes affected over 537 million people worldwide in 2021, with prevalence rising rapidly and healthcare costs reaching nearly $1 trillion annually.[2] Despite this, almost half of those with diabetes remain undiagnosed, particularly in low- and middle-income countries, heightening the risk of serious complications such as cardiovascular disease and kidney failure. Persistent hyperglycemia drives the development of microvascular complications such as nephropathy, neuropathy, and retinopathy through mechanisms involving oxidative stress, chronic inflammation, and the accumulation of advanced glycation end products, significantly worsening patient outcomes and straining healthcare resources.[3,4] Although conventional treatments such as insulin and oral hypoglycemic agents such as metformin and sulfonylureas effectively manage blood glucose levels, they are frequently accompanied by side effects ranging from gastrointestinal disturbances to liver toxicity. This underscores the urgent need for safer and more effective alternative therapies.[5,6] India’s rich heritage of ethnomedicine offers a vast repository of medicinal plants traditionally utilized to alleviate diabetic conditions with minimal adverse effects.[7] Various phytochemicals, including flavonoids, alkaloids, terpenoids, and polyphenols, have been identified as responsible for the antidiabetic properties of several botanical species.[8,9] The Kolli Hills region, located in Tamil Nadu’s Namakkal district, is renowned for its diverse flora and rich tribal knowledge pertaining to herbal remedies. The indigenous communities of Kolli Hills extensively rely on native medicinal plants for primary healthcare, including diabetes management.[9-11] Scientific evidence supporting traditional polyherbal antidiabetic remedies remains limited. Sooranam, a polyherbal ethanolic extract traditionally used in Kolli Hills for diabetes management, warrants systematic evaluation. This study investigates its antidiabetic potential using in vitro assays targeting key mechanism such as inhibition of carbohydrate-hydrolyzing enzymes and enhancement of cellular glucose uptake. By generating empirical data, the study aims to validate ethnopharmacological claims and support the development of plant-based therapeutic options that may complement conventional diabetes treatment.
MATERIALS AND METHODS
Collection of medicinal plants
Fourteen medicinal plants were collected from Kolli Hills, Namakkal District, Tamil Nadu, India. Authentication was performed by a qualified botanist from an institute in the western part of Tamil Nadu. The botanist’s formal training in systematic botany and extensive experience in identifying South Indian medicinal flora, supported by prior herbarium-based taxonomic work, ensured accurate authentication of all collected species. The selected plants were as follows: Azadirachta indica, Momordica charantia, Trigonella foenum-graecum, Ocimum sanctum, Aegle marmelos, Syzygium cumini, Zingiber officinale, Andrographis paniculata, Moringa oleifera, Tinospora cordifolia, Senna auriculata, Pterocarpus marsupium, Phyllanthus emblica, and Ocimum tenuiflorum. The present study was a purely in vitro investigation and did not involve human subjects, animal experimentation or clinical samples; therefore, ethical committee approval was not applicable to this study.
Preparation of ethanolic extracts
Plant materials collected from Kolli Hills were thoroughly washed with tap water followed by distilled water, then shade-dried at room temperature for 10–12 days. The dried materials were pulverized into a fine powder using a mechanical grinder and stored in airtight containers. For extraction, a measured quantity of the powdered material was packed in a Soxhlet thimble and extracted with 95% ethanol for 8–10 h until the siphon became colorless. The resulting extract was filtered using Whatman No. 1 filter paper and concentrated under reduced pressure with a rotary evaporator at 40–45°C. The semi-solid mass obtained was dried to constant weight in a desiccator and stored in amber-colored airtight containers at 4°C until further analysis. Working solutions were freshly prepared in suitable solvents before performing the in vitro assays.
Preliminary phytochemical screening
Standard qualitative tests were performed to detect alkaloids, flavonoids, saponins, tannins, phenolics, and steroids in the extracts.
α-amylase inhibition assay
The α-amylase inhibitory potential was determined as per the standard method with minor modifications. This test was conducted by following the methodology of Ghauri et al.[12] Test sample solutions of the 15PC extract, representing the polyherbal ethanolic combination prepared from 15 selected medicinal plant components of the Sooranam formulation, were prepared at concentrations of 10, 20, 40, 80, 160, and 320 µg/mL by dissolving the dried extract in 1% dimethyl sulfoxide (DMSO) and diluting with phosphate buffer (pH 6.8) to obtain the final working solutions. Acarbose, a clinically established inhibitor of both α-amylase and α-glucosidase, served as the positive control and was formulated at the same concentration range as the test extract. It is a well-known antidiabetic agent used to reduce postprandial hyperglycemia by delaying carbohydrate digestion.[13,14] A control solution without an inhibitor was included for comparison. The reaction mixture consisted of α-amylase solution and starch substrate, incubated at 37°C for 60 min. The reaction was terminated by adding 1N HCl, followed by Lugol’s iodine reagent (0.5% iodine and 1% potassium iodide), and the absorbance was recorded at 565 nm to determine the percentage enzyme inhibition.
The inhibition percentage was calculated using:
% Inhibition = ([Optical density of the control−Optical density of the sample]/Optical density of the control) × 100.
α-glucosidase inhibition assay
The inhibitory effect of the 15PC extract on α-glucosidase activity was assessed using p-nitrophenyl-α-Dglucopyranoside (pNPG) as the substrate, following a standard assay procedure with defined reaction composition. The dried ethanolic extract was dissolved in 1% DMSO and diluted with 50 mM phosphate buffer (pH 6.8) to obtain working concentrations (10–320 µg/mL). For each assay, a 200 µL reaction mixture was prepared consisting of 50 µL of the test sample, 50 µL α-glucosidase enzyme solution (1.0 U/mL in phosphate buffer; final activity 0.25 U/mL), 50 µL phosphate buffer, and 50 µL pNPG substrate (5 mM prepared in 50 mM phosphate buffer; final concentration 1.25 mM). The enzyme and extract were pre-incubated at 37°C for 10 min, after which pNPG was added to initiate the reaction. The mixture was then incubated at 37°C for 30 min, and the reaction was terminated by adding 100 µL of 0.1 M sodium carbonate. The release of 4-nitrophenol was quantified by measuring absorbance at 405 nm using a ultraviolet-visible spectrophotometer. Voglibose served as the positive control. The methodology was followed by Medabalimi et al.[15] The percentage inhibition of α-glucosidase activity was calculated in comparison with the control.
The inhibitory activity of α-glucosidase was calculated using the following formula,
% Inhibition = ([Absorbance of the Control−Absorbance of the Sample]/Absorbance of the Control) × 100.
Glucose uptake assay
Glucose uptake in yeast cells was assessed using a glucose depletion method. A 10% (w/v) yeast suspension was incubated with 50 mM glucose and varying concentrations of the 15PC extract at 37°C for 60 min. Following incubation, the mixture was centrifuged at 3000 rpm for 5 min, and the supernatant was collected for analysis. The absorbance of the supernatant was measured at 540 nm, representing the concentration of residual glucose remaining in the medium. Since yeast cells take up glucose during incubation, a lower absorbance value corresponds to greater glucose uptake, whereas higher absorbance indicates reduced uptake. Glucose uptake percentage was calculated by comparing the sample absorbance with that of the control.
RESULTS
The ethanol extract of Sooranam (15PC) was subjected to preliminary phytochemical evaluation, which confirmed the presence of flavonoids, phenolics, tannins, alkaloids, and saponins, while steroids were absent, indicating a rich profile of bioactive constituents commonly associated with antihyperglycemic activity. The extract exhibited significant inhibitory activity against both α-amylase and α-glucosidase in a dose-dependent manner. In the α-amylase inhibition assay, the extract produced 10.69%, 54.70%, 76.99%, 88.06%, 90.32%, and 91.56% inhibition at concentrations of 10, 20, 40, 80, 160, and 320 µg/mL, respectively, with an IC50 value of 23.70 µg/mL, whereas the standard Acarbose showed stronger activity with an IC50 of 10.84 µg/mL [Figure 1].

- The image illustrates the concentration-dependent inhibitory effect of the 15PC extract compared with the standard on α-amylase activity.
A similar trend was observed in the α-glucosidase assay, where inhibition increased steadily from 7.99% at 10 µg/mL to 92.67% at 320 µg/mL, closely approximating Voglibose, which showed 95.76% inhibition at the same concentration, although the standard remained more potent at lower levels, the extract’s inhibitory capacity became nearly comparable beyond 80 µg/mL [Figure 2]. Complementing its enzyme-inhibitory potential, the 15PC extract demonstrated strong glucose-uptake–enhancing activity in the yeast cell model, showing a concentration-dependent increase from 42.8% uptake at 0.5 mg/mL to 56.3% at 1 mg/mL, 68.4% at 2 mg/mL, and reaching a maximum of 81.7% at 5 mg/mL, indicating substantial reduction of extracellular glucose and suggesting improved transport across the yeast membrane [Figure 3]. Collectively, the extract exhibited robust antidiabetic activity across all in vitro models, with inhibitory effects on key carbohydrate-digesting enzymes and significant enhancement of glucose utilization, demonstrating a multifaceted mechanism supported by its rich phytochemical profile.

- This image displays the inhibitory activity of the 15PC extract and the standard drug Voglibose on α-glucosidase across increasing concentrations.

- This image displays the inhibitory activity of the 15PC extract and the standard drug Voglibose on α-glucosidase across increasing concentrations.
DISCUSSION
The ethanolic extract of Sooranam was analyzed for its phytochemical constituents to gain preliminary insight into its therapeutic potential. Qualitative screening confirmed the presence of alkaloids, flavonoids, phenolics, tannins, and saponins, while steroids were absent. These phytochemicals are noteworthy since they are frequently associated with antidiabetic mechanisms, such as the inhibition of carbohydrate-digesting enzymes, antioxidant protection, and enhancement of glucose utilization. The detected abundance of these compounds supports earlier findings that link the antidiabetic potential of medicinal plants to their ability to regulate glucose metabolism and alleviate oxidative stress-induced cellular damage.[16,17] Flavonoids and phenolic compounds, in particular, are known to act as antioxidants that can protect pancreatic β-cells from oxidative damage, enhance insulin secretion, and inhibit carbohydrate-hydrolyzing enzymes.[17,18] Despite being less potent than the standard, the extract showed relevant inhibitory action, suggesting a moderating effect on starch digestion. The α-glucosidase inhibition assay was then conducted to assess the extract’s impact on the final step of carbohydrate digestion. The moderate IC50 values observed for α-amylase (23.70 µg/mL) and α-glucosidase (40.75 µg/mL) inhibition suggest a physiological benefit comparable to other plant-based enzyme inhibitors such as Psiadia punctulata, Meriandra bengalensis, and Quercus coccifera, which also displayed dose-dependent enzyme inhibition in vitro.[18,19] Similar results were observed with ethanolic extracts of the Ayurvedic polyherbal formulation Shirishadi, where IC50 values for α-amylase and α-glucosidase were 0.68 and 2.89 mg/mL, respectively, confirming the ethnomedicinal rationale for using polyherbal formulations that target multiple carbohydrate-processing enzymes.[20]
Beyond enzyme inhibition, the extract showed strong glucose-uptake-enhancing activity in the yeast cell model. Glucose uptake increased steadily from 42.8% at 0.5 mg/mL to 81.7% at 5 mg/mL, demonstrating a marked dose-dependent improvement in cellular glucose transport. This enhancement indicates that the extract not only reduces glucose liberation during digestion but also facilitates intracellular glucose utilization, suggesting possible insulin-mimetic or insulin-sensitizing effects. Such combined actions are comparable to multitargeted antidiabetic mechanisms described for Q. coccifera and T. cordifolia, which exert simultaneous effects on enzymatic pathways and cellular glucose uptake.[19,21] The observed ability of the extract to lower extracellular glucose without apparent cytotoxicity aligns with previous reports that plant-based therapies can modulate glycemic parameters more gently than synthetic drugs, which often present greater gastrointestinal adverse effects.
Collectively, the phytochemical richness of the Sooranam extract appears to underpin its multi-targeted antidiabetic activity, encompassing inhibition of α-amylase and α-glucosidase as well as significant enhancement of glucose uptake. Although the extract is less potent than standard pharmaceutical agents on an IC50 basis, its combined enzymatic and cellular effects represent a meaningful therapeutic potential. These findings support the traditional use of polyherbal formulations in glycemic management and justify further investigations, including mechanistic studies, in vivo evaluations, and characterization of individual bioactive molecules responsible for the observed effects.
Limitations
Although this study provides valuable preliminary evidence supporting the antidiabetic potential of the Sooranam polyherbal extract, certain limitations should be acknowledged. The findings are based on in vitro assays, which serve as an important first step but cannot fully replicate the complexity of human metabolic pathways. The use of a crude extract without isolation of individual bioactive compounds limits mechanistic interpretation, and glucose uptake was evaluated only in a yeast model. Despite these constraints, the study offers a strong foundation for future in vivo research, compound isolation, and mechanistic exploration.
CONCLUSION
The ethanolic extract of Sooranam, a traditional polyherbal formulation from Kolli Hills, displayed significant in vitro antidiabetic activity by acting through multiple complementary mechanisms. Inhibition of both α-amylase and α-glucosidase occurred in a dose-dependent manner, while the extract also enhanced glucose uptake in the yeast cell model, suggesting an ability to modulate postprandial glucose metabolism as well as cellular glucose utilization. These effects are likely driven by its rich content of bioactive phytochemicals, such as flavonoids, phenolics, tannins, and alkaloids. Although the potency observed was lower than that of standard antidiabetic agents, the extract’s broad-spectrum and multi-target actions highlight its potential as a natural adjunct in diabetes care. These findings offer scientific support for the ethnomedicinal application of Sooranam in diabetes management and point to the need for further studies on bioactive compound isolation, mechanistic elucidation, and in vivo validation to realize its therapeutic promise. This extract may serve as a complementary therapeutic for early-stage diabetes.
Acknowledgment:
We express our sincere gratitude to the Department of Pharmacognosy for providing the facilities and support required for this research. We also express our thanks to the botanist for authenticating the medicinal plants collected from the Kolli Hills. Finally, we express our appreciation to all colleagues and staff who assisted throughout the experimental and analytical procedures.
Ethical approval:
The study was approved by Thangam Hospital – Institutional Ethics Committee, PGP College of Pharmaceutical Science and Research Institute, Namakkal, Tamil Nadu, India. Number: ECR/1069/Inst/TN/07/2024, Dated march 24, 2024.
Declaration of patient consent:
Patient’s consent was not required as there are no patients in this study.
Conflicts of interest:
There are no conflicts of interest.
Use of artificial intelligence (AI)-assisted technology for manuscript preparation:
The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.
Financial support and sponsorship: None.
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