However, none of the renal functional parameters were significantly altered after oral ingestion of ZAL and ZA. Histopathological

evaluation Liver histology of the control group showed well-preserved hepatocytes morphology; a well-maintained lobular array with central vein, radiating sinusoids and portal triads were all clearly observed (Figure 3E). The same findings were demonstrated in the treated group from all doses used (Figure 3A,B,C,D). In the case of mild or early liver insult, transferases and or phosphatase levels would be elevated without any clinical symptoms [26]. This may be followed by jaundice, encephalopathy, coagulopathy and possibly some microscopic changes on histology [26]. Here, only slight liver enzymes’ derangement was noted at higher doses of ZAL and ZA, and neither clinical nor microscopic evidences of liver toxicity followed. Figure selleck chemical 3 Microscopic Selleckchem MI-503 appearance of the liver stained

with H & E. Normal architecture of liver tissue after stained with H & E. The hepatocytes are well delineated with centrally located nucleus, seen in control and the four treated groups. This hepatic histology was taken at ×10 magnification from the rats 4 weeks post treatment with ZALH (A), ZALL (B), ZAH (C), ZAL (D) and vehicle control (E). The doses were given via oral route repeatedly over the 28 days study period. Portal triad (PT), central vein (CV), hepatocytes (H) and sinusoid (S). The hepatic lobular array is shown to be well maintained with central vein at the centre surrounded by many portal triads. The histology of the

spleen and brain was modestly similar in the control and experimental groups (Figures 4, 5, and 6). No remarkable changes were seen in the treated group that can be associated to nanodelivery systems ingestion. Two parts of the brain namely the cerebral click here cortex and the substantia nigra were stained and viewed, this is Selleckchem Rapamycin because of their importance in Parkinson’s disease and treatment [27]. Figure 4 Microscopic appearance of the spleen stained with H & E. Normal architecture of splenic tissue on light microscope after stained with H & E. The micrographs were taken at ×10 magnification in rats 4 weeks post treatment with ZALH (A), ZALL (B), ZAH (C), ZAL (D) and vehicle control (E). The doses were given via oral route repeatedly over a period of 28 days. White pulp (WP) and red pulp (RP) in experimental groups were shown to be similar in appearance compared to the control. Figure 5 Microscopic appearance of cerebral cortex stained with H & E. Histopathology of cerebral cortex (×10) in rats 4 weeks post-exposure to different concentrations of ZALH (A), ZALL (B), ZAH (C), ZAL (D) and vehicle control (E). The H & E stained micrographs showing cerebral cortex layers (CL), many neuronal cells and blood vessel (BV) on micrograph (E). Similar structural appearances were noted on all the four treated groups (A to D), thus no changes were seen in the cerebral cortex of the treated animals compared to control.