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Abstract

The present study investigates the anti-diabetic potential of Pterocarpus marsupium (heartwood extract) and Tecoma stans (leaf extract) in streptozotocin (STZ)-induced diabetic Wistar rats. Diabetes was induced via intraperitoneal injection of STZ (50 mg/kg). Rats were treated with individual extracts (200 mg/kg) and their combination for 21 days. Blood glucose, body weight, lipid profile, serum insulin, and histopathology of pancreatic tissue were evaluated. Both extracts significantly reduced fasting blood glucose and improved metabolic parameters. The combination group showed synergistic activity comparable to metformin. Findings support the potential of these plant extracts as complementary anti-diabetic agents.

Keywords

Pterocarpus marsupium, Tecoma stans, Diabetes, Streptozotocin, Metformin, Herbal extract

Introduction

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Diabetes mellitus is a chronic metabolic disorder characterized by persistent hyperglycemia due to defects in insulin secretion or action. Despite numerous synthetic anti-diabetic drugs, many have limitations including side effects and limited efficacy, prompting the exploration of safer, plant-based alternatives. Pterocarpus marsupium, commonly known as Indian Kino tree, has been traditionally used in Ayurvedic medicine for managing diabetes. Its heartwood contains active compounds such as pterostilbene and marsupsin that have β-cell regenerative and insulinogenic properties. Tecoma stans, a yellow trumpetbush, has shown hypoglycemic effects in preliminary studies due to its flavonoid and alkaloid content. This study aims to scientifically evaluate the individual and combined effects of P. marsupium and T. stans in STZ-induced diabetic rats.

Role of Insulin in glucose homeostasis

In addition to the direct effects of hyperglycemia on the uptake of glucose into both the liver and peripheral tissues, the hormone Insulin plays a central role in regulating the blood glucose concentration. The islet cell is freely permeable to glucose via GLUT-2 transporter and the glucose is phosphorylated by the high-KM glucokinase. Therefore, the blood glucose concentration determines the flux through glycolysis, the citric acid cycle and the generation of ATP. The concentration of insulin in the blood parallels that of the blood glucose. Insulin has an immediate effect of increasing glucose uptake in tissues such as adipose tissue and muscle. This action is due to an enhancement of glucose transport through the cell membrane by requirement of glucose transporter from the interior of the cell to the plasma membrane. Insulin does indirectly enhance long-term uptake of glucose by the liver as a result of its actions on the synthesis of enzymes controlling glycolysis, glycogenesis and gluconeogenesis. Insulin has an immediate effect in activating glycogen synthase.

MATERIALS AND METHODS

    1. Plant Material

Pterocarpus marsupium heartwood and Tecoma stans leaf was collected, shade-dried, powdered, and extracted using ethanol/water (70:30) by Soxhlet extraction. The dose used was 250 mg/kg body weight based on previous studies.

    1. Animals

Adult Wistar rats weighing 150–180 g was used after one week of acclimatization.

    1. Diabetes Induction

Diabetes was induced by a single intraperitoneal injection of STZ (50 mg/kg) after overnight fasting. Rats with fasting blood glucose (FBG) > 250 mg/dL after 72 hours were included.

    1. Grouping and Treatment

Table 1.1 Grouping and Treatment (Pterocarpus marsupium) We arranged same numbers of rats in each group like normal control, diabetic control, Pterocarpus marsupium treated, Tecoma stans treated, combination dose of pterocarpus marsupium and tecoma stans treated and last group is treated by standard drug metformin

S. No.

Group No.

Group Name

Description

1.

I

Normal Control

Non-diabetic, received saline

2.

II

Diabetic Control

STZ-induced, received saline

3.

III

PM Treated

STZ-induced, treated with P. marsupium

4.

IV

Standard Drug

STZ-induced, treated with Metformin (100 mg/kg)

Treatment duration: 21 days; oral dosing once daily.

Table 1.2 Grouping and Treatment (Tecoma stans)

S. No.

Group No.

Group Name

Description

1.

I

Normal Control

Non-diabetic, received saline

2.

II

Diabetic Control

STZ-induced, received saline

3.

III

TS Treated

STZ-induced, T. stans

4.

IV

Standard Drug

STZ-induced, treated with Metformin (100 mg/kg)

Table 1.3 Grouping and Treatment (Combination)

S. No.

Group No.

Group Name

Description

1.

I

Normal Control

Non-diabetic, received saline

2.

II

Diabetic Control

STZ-induced, received saline

3.

III

TS Treated

STZ-induced, treated with both extracts (125+125 mg/kg)

4.

IV

Standard Drug

STZ-induced, treated with Metformin (100 mg/kg)

  1. Parameters Evaluated
  1. Primary Outcomes

Fasting Blood Glucose (Days 0, 7, 14, 21), Oral Glucose Tolerance Test (OGTT), HbA1c at Day 21

  1. Secondary Outcomes

Lipid profile, Body weight, Pancreatic histopathology

  1. Experimental Data
  1. Fasting Blood Glucose (mg/dL) Fasting blood glucose (FBG) levels in normal, healthy rats typically range from 3.95 to 5.6 mmol/L (71 to 101 mg/dL). These levels can vary based on factors like fasting duration, sampling method, and the specific rat strain. 

Table 1.4 Fasting Blood Glucose (mg/dL) (Pterocarpus marsupium)

S. No.

Group

Day 0

Day 7

Day 14

Day 21

1.

Normal Control

92

90

88

85

2.

Diabetic Control

275

290

300

310

3.

PM Treated

265

210

165

120

4.

Metformin Treated

270

185

135

92

Table 1.5 Fasting Blood Glucose (mg/dL) (Tecoma stans)

S. No.

Group

Day 0

Day 7

Day 14

Day 21

1.

Normal Control

90

88

87

85

2.

Diabetic Control

270

285

295

305

3.

TS Treated

260

215

170

125

4.

Metformin Treated

270

190

130

95

Table 1.6 Fasting Blood Glucose (mg/dL) (Combination)

S. No.

Group

Day 0

Day 7

Day 14

Day 21

1.

Normal Control

90

88

87

85

2.

Diabetic Control

270

285

295

305

3.

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Verma Sanjivani
Corresponding author

Oriental University, Indore (M.P)

Photo
Dr. Bais Nidhi
Co-author

Oriental University, Indore (M.P)

Photo
Dr. Jain K. Sachin
Co-author

Oriental University, Indore (M.P)

Photo
Dr. Vengurlekar Sudha
Co-author

Oriental University, Indore (M.P)

Verma Sanjivani*, Dr. Bais Nidhi, Dr. Jain K. Sachin, Dr. Vengurlekar Sudha, Evaluation of Combination Study of Pterocarpus Marsupium and Tecoma Stans for Antidiabetic Action, Int. J. Sci. R. Tech., 2025, 2 (7), 88-95. https://doi.org/10.5281/zenodo.15806208

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