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Cardio-genic disruptions of in utero exposure of a non-fluoridated Cypermethrin (CP) and a fluoridated λ-Cyhalothrin (LC) type 2 pyrethroid insecticide were explored in albino mice. Pregnant dams were divided into three groups (n=10); 1) Vehicle Control Group (VCG) (intra-gastric treatment of 0.1mL corn oil); 2) Cypermethrin Group (CPG) and; 3) λ-Cyhalothrin Group (LPG) (intra-gastric treatment of 5mg/kg Cypermethrin (CP) and λ-Cyhalothrin respectively in corn oil). These treatments were applied on 7--10th days of pregnancy. Embryos were removed from the gravid uteri of the euthanized dams on 18th day of pregnancy and fixed in formyl ethanol for 24hrs to finally remove their hearts for histological and histometric analyses. Both insecticides were found to cause micro-anatomical derangements like decreased ventricular wall thickness, rudimentary appearance or complete absence of inter-ventricular (AV) septa, abnormalities of the cardiac valves, and decreased thickness of the muscular layer of the aortic trunk. However, these disruptions were much more pronounced in LCG. Morphometric results revealed a significant decrease (P>0.05) in the thickness of left ventricular wall in CPG (295.90±12.3µ) and LCG (104.27±5.6µ) as compared to VCG (346.68±9.5µ). The mean thickness of interventricular septum was significantly decreased in CPG (440.03±20.4µ) and LCG (214.3±10.2µ) groups than the VCG (2641.75±186.2µ). The thickness of the aortic intima also showed a significant (P>0.05) decrease in CPG (12.70±0.25µ) and LCG (11.03±0.3µ) than the VCG (18.44±0.37µ). Similarly, the thickness of aortic adventitia remained significantly (P>0.05) lower in CPG (26.96±1.1µ) and LCG (23.97±1.5µ) than the VCG (41.09±2.1µ). The relative abundance of myocardiocytes and cardio-myoblasts (per 5000µ2) also showed significant decrease in both CPG (8.98 ±0.45, 2.50±0.24 respectively) and LCG (4.7 ±0.48, 6.26±0.79) to the VCG (18.19±0.56, 1.02±0.13). The results show that type-2 pyrethroid insecticides inflict a highly toxic impact on the developing heart in mammals and the fluoridated LC is more toxic than the CP in this context. [ABSTRACT FROM AUTHOR]

This study was designed to investigate testicular and male reproductive tract histopathologies and lipid profile against di‐ethylhexyl phthalate (DEHP) exposure in mice and curative potentials of aqueous garlic (Allium sativum) extract. Four groups (n = 10) were named and treated as follow (a) control (C): (normal feed and drinking water + 0.2 ml corn oil); (b) aqueous garlic extract group (AGE): (500 mg/kg body weight of aqueous garlic extract); (c) DEHP group: (500 mg/kg body weight of DEHP, dissolved in corn oil; (d) AGE + DEHP group (500 mg/kg body weight garlic aqueous extract, and DEHP 500 mg/kg body weight dissolved in corn oil). The doses were given once daily through gavages for 28 days and on the 29th day, all the animals were euthanized through cervical dislocation and reproductive organs and blood samples were collected. The results showed that exposure to DEHP caused a significant effect on body weight, testicular weight, serum cholesterol, triglycerides, lipid profile, average cross‐sectional area (ACSA) of the seminiferous tubule, ACSA of the lumen of seminiferous tubule, spermatogenic cells, Leydig's cells number, vas deferens diameter, lumen, muscular thickness, and epithelial cell height of vas deferens. This study revealed that exposure to DEHP can be injurious to male reproductive health and aqueous garlic extract can decrease the toxic effects of DEHP in male mice. [ABSTRACT FROM AUTHOR]

The objective of the present research was to determine if dibutyl phthalate (DBP) and di-(2-ethylhexyl) phthalate (DEHP) alone and combined exposure induced pathological alterations in laboratory reared albino mice. Adult male mice were equally divided (n = 10) into Control, corn oil (CO), DBP, DEHP, and DBP+DEHP treated groups. Dibutyl phthalate (250 mg/kg), DEHP (300 mg/kg), and DBP+DEHP (250+300 mg/kg), respectively, were administered by oral gavage mixed in corn oil (0.2 mL) for 28 days. All animals were sacrificed following 28 days of treatment and blood was collected for serum lipid profiles and liver function tests. Liver samples were also collected for observation of histological changes. Microphotographs of hematoxylin and eosin-stained sections were used for computer-based micrometry. CO, DBP, DEHP, and DBP+DEHP treatment resulted in a significant increase in the mean body and liver weights as compared with the Control group. Histological examination of the livers with DBP and/or DEHP treatment showed marked alterations leading to hepatic hypertrophy. In the treated groups, a significant increase in the mean number of mononucleated, binucleated cells, and oval cells per unit area was noticed with disorganized trabecular arrangement as compared with the Control group. Treatment with DBP and/or DEHP resulted in large regeneration zones in the liver and an increased relative nucleo-cytoplasmic index of mononuclear shepatocytes when compared with the Control group. All treatments caused a significant increases in the liver enzymes and proteins as well as altered serum cholesterol, triglycerides, LDL, and VLDL levels. The histopathological and serological findings confirmed the toxic potentials to hepatic tissue of DBP and DEHP either given alone or in combination. [ABSTRACT FROM AUTHOR]