Immunotoxicity Following Pre- and Post-natal Aluminum Exposure in Rats

• Published in: Toxicological research (Seoul) Vol. 24; no. 1; pp. 51 - 58
• Main Authors: Khalaf, Abd El-Azeim A. (Cairo University, Giza, Egypt), Morgan, Ashraf M. (Cairo University, Giza, Egypt), E-mail: Ashrafmrgn@yahoo.com, Mekawy, Mohey M. (Cairo University, Giza, Egypt), Ali, Maged F. (Cairo University, Giza, Egypt)
• Format: Journal Article
• Language: English
• Published: Singapore 한국독성학회 01.03.2008; Springer Singapore
• Subjects: Aluminum chloride; BAZO; Biomedicine; FOIE; HIGADO; Humoral and cell mediated immune response; Immunotoxicity; LIVER; Pharmacology/Toxicology; RAT; RATA; RATE; RATS; SPLEEN; Thymus; Spleen; Humoral and cell mediated immune response; Aluminum chloride; Liver; Immunotoxicity; Rats; Thymus
• ISSN: 1976-8257; 2234-2753
• DOI: 10.5487/TR.2008.24.1.051

The present study was designed to explore the immunotoxic effects of orally administered aluminum (AI) on pregnant rats (n = 60) and their growing fetuses and consequently on the animal wealth. The animals were randomly allocated into three equal groups of 20 rats each. The first group has no treatment and kept as a control (G1). The second and third groups of pregnant rats were treated orally with aluminum chloride at 345 mg/kg b.wt. The second group (G2) received the tested compound from the 6∨th day of gestation to the end of weaning, whereas the third group (G3) received the tested compound from the 15∨th day of gestation to the end of weaning. Control and treated animals (dams and offspring) were immunized ip with (0.5 ml) 20% sheep red blood cell (SRBC) suspension seven days before the end of experiments. At the end of exposure, ten dams and ten offspring from each group were used for assessment of cell-mediated immunity and a similar number of animals were sacrificed for evaluating the humoral immune response and serum protein profile. Aluminum chloride exposure of dams (G₂and G₃) caused significant suppression of both cell mediated and humoral immune responses in the obtained offsprings compared to the control group (G₁) without any significant effect on the immune responses of these dams. Moreover, the serum total globulins, albumin/ globulin (A/G) ratio and gamma globulin fraction were significantly decreased in the treated dam's offsprings compared to the corresponding controls while the serum total protein and all serum protein fractions showed non significant difference between the control and treated dams and between the two treated dam groups themselves. There were no histopathological changes observed in thymus, spleen and liver of the control and treated dams. Thymus of treated dam's offsprings (G2) showed lymphoid depletion in both cortex and medulla. Their spleens showed lymphoid depletion in the white pulps and congestion with hemosiderosis in the red pulps. Liver of treated dam's offsprings showed dilation and congestion of its central vein with degenerative changes in the hepatocytes. These histopathological changes were more severe in G2 than in G3 offsprings. It can be concluded that gestational and/ or lactation exposure of pregnant dams to AI chloride caused suppression of both cellular and humoral immune responses of their offsprings.