Aim: To determine the effects of chromatographic fractions of Abrus precatorius leaf extracts on the histology of the ovary and uterus.
 Study Design: Abrus precatorius plant contain woods in a twinning form and belong to the Fabaceae (Leguminosae) family. It has red and black seeds. Abrus precatorius also possess a pod which is short and stout brownish in color [1]. The plant grows in bushes and farm and sometimes in hedge. Abrus precatorius are said to be taken for tuberculosis and painful swellings [2]. According to Ross [3], they can be used as laxative, expectorant and aphrodisiac medicines and are sometimes used in urticaria, eczema, stomatitis, conjunctivitis, alopecia areata, migraine, lymphomas/leukemia and dysmenorrhea. Experiment has demonstrated that the seed have the ability to retard fertility both in male and female [4]. Studies done in the past revealed that the plant Abrus precatorius can kill cells or cause cell death at the same time leading to death of tumor [5]. Extraction of the leaves of A. precatorius with methanol has shown through previous study to possess bronchodilatory effect and its use traditionally in the management of asthma [6]. Extracts obtained from the roots, has good antibacterial activity especially against Staphylococcus aureus (Prabha et al. 2015). In a study performed in Tanzania, it was confirmed that boiling the leaves of A. precatorius with water and taking it orally as three table spoonful in twice daily dosage regimen for the treatment of epilepsy is helpful [7].
 Female wistar rats were treated with chromatographic fractions of A. precatorius, F1, F2, F3 and F4 (30 mg/kg, 60 mg/kg, 90 mg/kg, 120 mg/kg and 150 mg/kg) for thirty days. One hundred and ten Wistar rats were divided into twenty-two (22) groups of five rats each. All the rats were weighed before and during the experiment. Group 1 (Control) received 0.5 mls, Phosphate Buffer Solution (PBS); Group 3-7. received 30 mg/kg, 60 mg/kg, 90 mg/kg, 120 mg/kg and 150 mg/kg of F1. Group 8-12 received 30 mg/kg, 60 mg/kg, 90 mg/kg, 120 mg/kg and 150 mg/k of F2. Group13-17 received 30 mg/kg, 60 mg/kg, 90 mg/kg, 120 mg/kg and 150 mg/kg of F3 and Group 18-22 received 30 mg/kg, 60 mg/kg, 90 mg/kg, 120 mg/kg and 150 mg/kg of F4 respectively. The fractions/drugs were administered orally. The rats were treated with chromatographic fractions of A. precatorius, F1, F2, F3 and F4 (30 mg/kg, 60 mg/kg, 90 mg/kg, 120 mg/kg and 150 mg/kg) for 30 days. The animals were sacrificed, dissected and the uterus and ovaries obtained for histology study. The study revealed histological evidence that the chromatographic fractions of Abrus precatorius leaf do not have any potential adverse effect on the ovary and uterus of the Wistar Albino rats.