Diabetes is a complex metabolic disorder and different environmental toxicants including heavy metals have been involved in diabetes induction. Therefore, assessment of the environmental risk factors and heavy metals induced toxicity have become critical for reducing the consequences of metals pollutants. Previously, we reported heavy metals induced nephrotoxicity in non-diabetic and diabetic rats. Here, we extended our analysis by examining the heavy metals induced organs (heart, kidney, liver, pancreas, and spleen) damage in diabetic and non-diabetic Wistar rats using histopathology and quantitative real-time PCR (qRT-PCR). Following the generation of the diabetic rat model, the animals were exposed to heavy metals including lead (Pb), arsenic (As), manganese (Mn) and cadmium (Cd). Both non-diabetic and diabetic rats were exposed to heavy metals for 30 days and subsequently, the heart, kidney, liver, pancreas and spleen tissues were examined. Heavy metal treatment resulted in irregularly arranged myofibrils and vacuolization in the heart tissue of metal treated groups as evident from hematoxylin and eosin (H & E) staining. The kidney tissue of rats treated with heavy metals showed tubular degeneration, fibrosis, hemorrhage, and vacuolation. The liver of the heavy metals treated rats exhibited cellular degeneration and necrosis. The pancreatic tissue of streptozotocin injected untreated and metal treated rats revealed severe degeneration, necrosis, degranulation, shrinkage, and depression in the islets of Langerhans. Increased red pulp area and congestion were observed in the spleen of the metal mixture treated non-diabetic and diabetic rats. In line with the histological data, the qRT-PCR analysis showed downregulated expression of Bcl 2 and upregulation of Caspase-3 in nondiabetic and diabetic metal treated rats as compared to the non-diabetic untreated rats. In conclusion, the present study revealed, diabetic rats are more prone to metal alone as well as metal mixture induced organ damage as compared to non-diabetic rats. Diabetes is a metabolic disorder, characterized by impaired insulin secretion, fasting hyperglycemia or insulin receptor insensitivity. The prevalence of diabetes is increasing all over the world and increased from 4.7% in 1980 to 8.5% in 2014 1. Diabetes is the 7 th leading cause of mortality in the United States and worldwide and results in serious complications including kidney disease, cardiovascular disease, blindness, etc. 1,2. It is well documented that environmental exposure to synthetic or naturally occurring chemical elements contribute to diabetes induction 3-5. Metals are essential components of biological functions, while their higher concentrations can be toxic 6,7. Cadmium (Cd), arsenic (As), cobalt (Co), mercury (Hg), manganese (Mn) and lead (Pb) are known as endocrine-disrupting chemicals 8,9. Importantly, Pb, As, Mn and Cd play a crucial role in public health issues 10 .