Acute toxicity and histopathology study of a galactose-specific lectin from the seeds of Tetracarpidium conophorum (African walnut) (Hutch and Dalz)

A lactose-binding lectin (TCL) was purified from the seeds of African walnut, Tetracarpidium conophorum, and acute toxicity studies of the lectin were carried out with Swiss albino male mice. Animals were administered doses of TCL from 500 to 2500?mg?kg^?1 body weight (b.wt.) orally while intraperitoneally the dose ranged from 10 to 600?mg?kg^?1 b.wt. Animals were then assessed for organ and body weight changes, mortality, and histopathology. TCL did not cause any observable toxicity via the oral route; however, when administered intraperitoneally, TCL elicited toxicity with an LD₅₀ of 50?mg?kg^?1 b.wt. Death from intoxication was preceded by convulsion, hypoactivity, salivation, ataxia, and weakness. The animals given lethal doses of the lectin showed profound respiratory depression which was judged to be the primary cause of death. Histopathological analysis indicated that the lungs, liver, and spleen were adversely affected while the kidney and other organs were essentially normal. In all the affected organs, the severity of toxicity was dose-dependent as the effect of the lectin became more pronounced with increase of the dose administered.     

Bromobenzene-induced hepatotoxicity in male rats: the protective effect of flaxseed

The metabolites of bromobenzene (BB) are hepatotoxic. The aim of this study was to determine the efficacy of different doses of flaxseed extract in alleviating BB-hepatotoxicity in male albino rats. Oxidative stress parameters, drug metabolizing enzymes, a pro-inflammatory marker, an apoptotic marker, and DNA fragmentation pattern were also assessed. Animals were divided into five groups treated by intragastric intubation as follows: control, BB-treated 460?mg?kg^?1?BW alone; three animal groups (III, IV, V) were treated concurrently with 460?mg?kg^?1 BB daily for 3 weeks and different doses of flaxseeds extract: 100, 200, or 300?mg?kg^?1?BW. Oral treatment of BB produced a significant decrease in activities of antioxidant enzymes superoxide dismutase and glutathione peroxidase and glutathione levels, while activities of glutathione reductase and drug-metabolizing enzymes; glutathione-S-transferases and cytochrome P450 were enhanced. BB-treatment resulted in enhanced production of nitric oxide and activation of COX-2 and caspase-3. Pre-treatment with different doses of flaxseeds extract prior and during BB-treatment protected liver against BB-induced hepatotoxicity. The lower dose of flaxseed extract (100?mg?kg^?1) was most effective one.     

Histopathological effects of artemether on selected organs in rat

Dose and treatment-duration neurotoxic effects are reported for artemisinin drugs of mostly the liposoluble derivatives; and yet artemether, the only parenteral formulation of the artemisinin series available in Nigeria is fat-soluble and also has a treatment-duration of 5–7 days (in an attempt to delay recrudescence). Since parenteral drugs are usually resorted to in severe/complicated or multidrug-resistant malaria against the oral artemisinin co-formulated therapies (ACT), this study is aimed to investigate the pathological changes on selected tissues (if any), in rats, of the normal 7-days artemether-injections when used both in the normal and higher doses. Artemether was administered i.p., at three dose levels, equivalent to therapeutic dose (1.5 mg kg^?1) as well as 5 and 10 times higher (7.5 and 15 mg kg^?1). A three percentage v/v Tween 80 vehicle was used for the control experiment. The pathological changes in the kidney, heart, liver, and lungs evaluated using percentage mean organ:body-weight ratio showed no changes in the organs. No histopathological effect was observed in the organs of rats treated with 1.5 mg kg^?1. However, rats treated with 7.5 and 15 mg kg^?1 revealed necrositic lesions with mononuclear cellular-infiltration in the liver and brain. The liver had focal area necrosis, while the brain had liquefactive necrosis, neuronal degeneration, congested blood vessels, hemorrhage, and vacuolations. The interstitial spaces of the glomerulus and renal tubules of one kidney from rats that received 15 mg kg^?1 had focal area fibrositic-necrosis.     

Protective effects of curcumin on antioxidant status,body weight gain,and reproductive parameters in male rats exposed to subchronic 2,3,7,8-tetrachlorodibenzo-p-dioxin

The aim of this study was to investigate the effects of curcumin (CUR) on antioxidant status, body weight (BW) gains, and some reproductive parameters in male rats exposed to subchronic doses of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Thirty-two rats were divided into four groups. The first group was kept as control. The second group (TCDD group) was given TCDD at a dose of 50 ng·kg^?1 BW per day; the third group (CUR group) was treated with CUR at a dose of 80 mg·kg^?1 BW per day. The fourth group (TCDD + CUR group) was given TCDD and CUR at the same doses simultaneously. Malondialdehyde (MDA) levels were significantly increased in the TCDD group. In addition, TCDD exposure decreased liver superoxide dismutase (SOD) activity, catalase (CAT) activities of kidney and brain, glutathione peroxidase (GSH-Px) activities of liver, kidney, and brain, and glutathione levels of liver, kidney, and heart. However, CUR treatment with TCDD exposure decreased MDA levels in all tissues and increased SOD activities of liver, kidney, and brain, CAT activity of heart, and GSH-Px activities of heart and brain. TCDD caused a decrease in BW gain, and CUR partially eliminated this effect of TCDD. In addition, while reproductive organ weights, sperm concentration, and sperm motility tended to decrease with TCDD exposure, these effects tended to be close to normal levels by CUR treatment. In conclusion, CUR was seen to be effective in the treatment and prevention of toxicity induced by subchronic TCDD exposure.     

Chlorpyrifos induces oxidative stress in rats

This study was carried out in male Wistar rats to determine the potential effects of chlorpyrifos (CHP) on oxidative stress, as was reported for organophosphorus (OP) pesticides. Following an acute, daily 3- or 14-day exposure with CHP at doses of 2.5, 5, or 25 mg kg^?1 data showed significant increases in malondialdehyde levels at both exposure durations and at all doses, except for 2.5 mg kg^?1, in hepatic and aorta, kidney, and plasma samples. The nitrites (NO) showed elevation at 25 mg kg^?1 in aorta, at 3- and 14-day exposure, in hepatic tissue with all doses at 3-day exposure, but not at 14-day with a 5 mg kg^?1 dose. In plasma, increases occurred only at 25 mg kg^?1 at both exposure times, and in kidney at all doses and both exposure durations. Superoxide dismutase (SOD) enzyme activity in the aorta sample was statistically significant at all doses at 3 days and at 14 days, except at 2.5 mg kg^?1; and in hepatic tissue only at 25 mg kg^?1 dose at both durations. In plasma SOD activity was elevated at all doses at 3 days, but at 14 days only at 25 mg kg^?1. Data suggests that oxidative stress may be involved in the effects of CHP on rats.     

Persistence of chlorpyriphos in okra (Abelmoschus Esculentus) fruits and soil

Persistence of cypermethrin and chlorpyriphos in okra and soil were studied following the application of pre-mix formulation of insecticides Action 505EC (chlorpyriphos 50%?+?cypermethrin 5%) at single (275?g a.i.?ha^?1) and double dose (550?g a.i.?ha^?1). The average initial deposits of chlorpyriphos in okra were observed to be 0.07 and 0.15?mg?kg^?1 in single and double dose, respectively, which dissipated to 92% after 10 days for both the dosages. Residues of soil under okra crop were found to be 0.15?mg?kg^?1 at the single and 0.36?mg?kg^?1 at the double doses. These residues persisted up to 3 days at single and 5 days at double dose. The half-life (t _1/2) periods of chlorpyriphos on okra and soil were observed to be 0.6 days and 1.9 days for single and double dose, respectively. Residues of chlorpyriphos reached below detectable level (BDL) of 0.01?mg?kg^?1 in okra fruits after 7 days at single dose and in 15 days in double dose. In soil, residues of chlopyriphos persisted up to 5 and 7 days in single and double dose, respectively. Following foliar applications of a insecticide formulation (Action 505EC, (chlorpyriphos 50%?+?cypermethrin 5%) on okra at @ 275 and 550?g active ingredient (a.i.)?ha^?1 resulting in active applications of chlorpyriphos at the rate of 250 and 500?g a.i.?ha^?1 the average initial deposits of chlorpyriphos in okra were observed to be 0.07 and 0.15?mg?kg^?1, respectively. These residue levels dissipated to 92% after 10 days at both the dosages. Residues of soil under the okra crop were found to be 15?mg?kg^?1 at the single and 36?mg?kg^?1 at the double dose. The residues persisted up to 3 days at the single and 5 days at the double dose. The half-life (t _1/2) periods of chlorpyriphos on okra were observed to be 0.6 days for application rates, and 1.9 days for soil. Okra fruits and soil samples collected on the 7th and 15th day after application did not show any chlorpyriphos residues above their determination limits of 0.01 and 0.005?mg?kg^?1, respectively.     

Protective efficacy of Mucuna pruriens extract on Epichlorohydrin induced toxicity in epididymis of albino rats

The protective effects of seeds of Mucuna pruriens on epichlorohydrin (ECH)-induced toxicity in epididymis and epididymal sperms of rats were studied. Different doses of ECH and M. pruriens (75 and 100 mg kg^?1, respectively) were administered daily, orally for 70 days. Group I animals served as control. Group II and III rats received ECH (75 or 100 mg kg^?1 body weight, respectively) alone. The group IV and V rats received a combination of both ECH and the seed extract of M. pruriens at 75 or 100 mg kg^?1 body weight. Group VI rats was administered only the extract of M. pruriens 100 mg kg^?1 body weight. At the end of the experiment (71st day), rats were sacrificed and sperm collected from epididymis were used for the assessment of sperm count, sperm viability, and sperm motility. Administration of ECH produced a reduction in epididymal sperm count, sperm viability, and sperm motility. The activities of catalase, superoxide dismutase, and glutathione peroxidase were decreased, while lipid peroxidation was increased. ECH produced a decrease in the levels of protein, acid phosphatase, sialic acids, and increased the level of alkaline phosphatase, and cholesterol. The administration of M. pruriens to ECH-treated rats resulted in a protective effect.     

Determination of metals in printed wiring boards of waste mobile phones

Metal contents of waste mobile phones represent a major environmental risk, especially considering the adoption of inappropriate management options in developing countries including open burning and disposal into surface water bodies. In this study the metal contents of mobile phone printed wiring board (PWB) samples were assessed. Sixty-two waste mobile phones of 15 brands were collected, dismantled, and their PWB samples were analyzed for Cu, Pb, Ag and Cd. The metal concentrations in the samples varied widely between and within brands. Among these metals, Cu and Pb were found to be at very high concentrations. The range (mean?±?SD) of Cu and Pb concentrations were 94.1–532?g?kg^?1 (250?±?92.3?g?kg^?1) and 7.0–46.2?g?kg^?1 (20.1?±?8.4?g?kg^?1), respectively. All Cu and Pb concentrations exceeded toxicity threshold limit concentration (TTLC) regulatory limits used in characterizing wastes as hazardous in the state of California, USA. The mean Cu and Pb concentrations exceeded the corresponding TTLC limits by factors of 100 and 20, respectively. The Ag and Cd concentrations were in the range 59.4–759?mg?kg^?1 (mean 227?±?104?mg?kg^?1) and ND – 15.6?mg?kg^?1 (2.1?±?3.3?mg?kg^?1), respectively.     

Toxicological studies of zinc oxide nanomaterials in rats

In this study, we have evaluated the ability of zinc oxide (ZnO) nanoparticles to induce pulmonary and extrapulmonary toxicities was examined in rats following intratracheal (IT) instillation. Lungs of rats were instilled IT with either phosphate-buffered saline (PBS)?+?1% Tween 80, ZnO nanoparticles, carbonyl iron or quartz particles at a dose of 1 or 5?mg?kg^?1 body weight. Following exposure, bronchoalveolar lavage (BAL) fluid, blood samples and organs including lung, liver, kidneys, heart, pancreas, and brain were collected at 24?h, 1 week, or 1 month of post instillation of nanoparticles and different parameters estimated to assess toxicity. BAL fluid was analyzed for lactate dehydrogenase (LDH) and alkaline phosphatase (ALP) to assess pulmonary toxicity. Exposures to ZnO or quartz particles produced transient dose-dependant increase in BAL fluid LDH and ALP activities at all post exposure periods. Blood samples were analyzed for the tissue damage biomarkers to assess extrapulmonary toxicity. Histopathological examination of lung, liver and kidneys revealed dose-dependent degeneration and necrosis which worsened at 1 week post-instillation periods but recovered at 1 month post instillation. Histopathological examination of rat pancreas, heart, and brain exposed to quartz or ZnO particles showed no marked changes. Data suggest the instillation of ZnO nanoparticles produced a greater pulmonary toxicity in rats comparable with quartz; and extrapulmonary toxicities of these ZnO nanoparticles might be due to translocation into liver and kidney.     

Effects of dietary copper exposure on accumulation,growth, and hematological parameters in Cyprinus carpio

The influence of dietary copper (Cu) exposure on accumulation, growth, and hematological parameters was investigated in Cyprinus carpio after sub-chronic ingestion of 0, 250, 500, 750 or 1000?mg?kg^?1 for 60 days. The profile of Cu accumulation among tissues in C. carpio was dependent on the exposure period and Cu concentration. Liver of C. carpio was the predominant storage tissue and the order of Cu accumulation in tissues was liver?>?intestine?> gill?>?kidney?>?muscle. Cu concentration at >125?mg?kg^?1 reduced growth rate, and was inversely related to growth. The RNA?:?DNA ratios were not affected by exposure and there was no correlation between growth rate and RNA?:?DNA ratio in liver and muscle. There were no significant effects of exposure on blood parameters except for magnesium. Cu exposure time and dose increased the serum glutamic-oxaloacetic transaminase (SGOT) and serum glutamic-pyruvic transaminase (SGPT) activity levels.     

Exposure of mallards ( Anas platyrhynchos ) to the hepatotoxic cyanobacterium Nodularia spumigena

Nodularin (NODLN) is a cyclic pentapeptide hepatotoxin produced by the cyanobacterium Nodularia spumigena, which forms extensive blooms during the summer in the Baltic Sea. Nodularin was detected in liver, muscle and/or feather samples of several common eiders (Somateria mollissima) from the Gulf of Finland (northern Baltic Sea) in 2002–2005. Published information on the adverse effects of NODLN in marine birds is scarce. The aim of this study was to evaluate the toxicity of NODLN, and determine the concentrations of NODLN in liver and muscle tissue in mallards (Anas platyrhynchos) exposed to N. spumigena. Mallards received a single or multiple exposure via oral gavage with an aqueous slurry containing toxic N. spumigena. Dosages ranged from 200 to 600 µg NODLN per kg body weight (bw). There were minimal histopathological changes in liver tissue, and brain cholinesterase activity did not differ among treatment groups. Concentrations of NODLN measured by LC-MS in liver varied between approximately 3–120 µg kg^?1 dry weight (dw) and ducks receiving multiple exposures had significantly greater liver toxin levels than ducks receiving the two lowest single exposures. In muscle, NODLN concentrations were approximately 2–6 µg kg^?1 dw, but did not differ significantly among exposure groups. This is the first in vivo lab study examining the effects and bioaccumulation of NODLN from N. spumigena in birds. The mallards in this study were resistant to adverse effects and did not bioaccumulate substantial levels of NODLN at the doses given.     

In vitro genotoxicity of extracellular extract from Nostoc piscinale

The extracellular extract obtained from 3 weeks incubation of the soil isolate cyanobacterium strain Nostoc piscinale GT-319 in BG-11 broth medium showed cytotoxic activity against Chinese Hamster Ovary (CHO) cells. Based on comet assay, a concentration of 333 µg mL^?1 (IC₅₀) produced DNA breakages in CHO cells. The concentration of 481 mg kg^?1 (LD₅₀) produced acute toxicity in mice at 48 h.     

Essential and nonessential elements in the red-crowned crane Grus japonensis of Zhalong Wetland,northeastern China

The concentrations of four essential (Ca, Mg, Zn, and Cu) and two nonessential elements (Pb and Cd) in feathers and kidneys, livers, gut walls, and muscles of eight carcasses of migratory red-crowned cranes (Grus japonensis) from Zhalong Wetland, northeastern China, were examined. The concentrations of Cd in the feathers were between 0.4 mg kg^?1 dry weight (dw) and 3.1 mg kg^?1 dw, in the livers between 0.4 and 4.4 mg kg^?1 dw, the maximum of which exceeded a level considered to be environmental exposure risk (i.e., 3 mg kg^?1 dw in the liver or kidney). High Pb levels (0.4–3.2 mg kg^?1 dw, with an average of 1.8 mg kg^?1) were also detected in livers, which exceeded a level considered toxicosis in birds (1.7 mg kg^?1 dw). Pb and Cd had the highest scores in principal component analysis. Relatively high Pb and Cd concentrations in the migratory cranes were thought to be associated with their habitat and prey.     

Protective role of Curcuma longa extract and curcumin on mercuric chloride-induced nephrotoxicity in rats: evidence by histological architecture

Mercury (Hg) is a potent nephrotoxin. The aim of this study was to investigate the protective role of Curcuma longa extract and curcumin against HgCl₂-induced nephrotoxicity. Male Sprague Dawley rats were administered HgCl₂ (12 μmol kg^?1, ip; once only) followed by treatment of Curcuma longa extract (200 mg kg^?1, po) and curcumin (80 mg kg^?1, po) for three days after 24 h of HgCl₂ administration. The present results showed that mercuric chloride administration caused an impairment of renal function system which was evident from significant increase in urea, creatinine, uric acid, and blood urea nitrogen concentration in serum. In addition, the swelling in glomerulus and degenerated renal tubules with obstructed lumen was also observed by acute mercuric chloride administration. Treatment with Curcuma longa extract and curcumin was effective in restoring all variables of kidney functions near to control group, which was consistent with kidney histoarchitecture. In conclusion, these results suggest that Curcuma longa extract and curcumin protect against HgCl₂-induced nephrotoxicity. This study could be important for the further understanding of mercury toxicity in renal tissues and in the development of better treatments for people and/or animals exposed to the metal.     

Toxicokinetics,metabolism, and microsomal studies of chlorpropham in rats

A study on the toxicokinetic behavior, metabolism of chlorpropham, and its effect on cytochrome P₄₅₀ from liver microsomes was carried out in albino rats after a single and consecutive oral administration at 500?mg?kg^?1 body weight for 10 and 20 days. Chlorpropham was detected in the blood at 0.08?h (11.43?±?1.72?µg?mL^?1) reaching a maximum concentration at 2?h (30.90?±?2.55?µg?mL^?1) and a minimum at 48?h (1.95?±?0.20?µg?mL^?1) after a single oral administration of 500?mg?kg^?1. The absorption rate constant (K _a) was 0.66?±?0.48?h^?1. The Vd _area (18.01?±?2.78?L?kg^?1) and t _1/2 β (12.23?±?1.96?h) values suggested a wide distribution and long persistence of the compound in the body, respectively. The higher Cl_R (0.82?±?0.00?L?kg^?1?h^?1) compared to Cl_H (0.18?±?0.02?L?kg^?1?h^?1) value indicated that a major portion of chlorpropham was excreted through the urine (30%) compared to the faeces (2.81%). Chlorpropham residue was detected in all tissues of rat at 0.25?h while its metabolite, meta-chloroaniline was detected in liver, kidney, heart, lung, and spleen tissue at 0.25?h. Meta-chloroaniline was not detected in skeletal muscle, brain, fat, and stomach tissue at any time of the observation period. Maximum concentrations of chlorpropham and meta-chloroaniline were detected at 2?h (except in the spleen), and minimum concentrations of chlorpropham at 24 (heart, lung, spleen, skeletal muscle, and stomach) and 48?h (liver, kidney, brain, and fat tissue) respectively; and meta-chloroaniline at 24?h (except heart and spleen). The tissue half-life of chlorpropham in rat varied from 3.80 to 11.60?h. Repeated oral administration of chlorpropham at 500?mg?kg^?1 for 10 and 20 days caused an induction of the liver microsomal pellet of rat.     

The deployment of γ-irradiation for reducing polycyclic aromatic hydrocarbons and microbial load in wheat kernels

Food contamination may contribute to serious human health problems. In this work, the effect of γ-irradiation 0, 5, 10, and 15 kGy doses on the removal of polycyclic aromatic hydrocarbons from wheat kernels was investigated. Additionally, variations in the contents of 16 congeners on bacterial load and other chemical parameters were studied. Polycyclic aromatic hydrocarbons concentrations were determined by high-performance liquid chromatography followed by fluorescence detection. The effects of γ-irradiation on the concentrations varied for each congener, with the highest irradiation dose being the most effective. Benzo[a]pyrene was reduced by ～50%, and the total concentration of all congeners decreased dramatically from 154 to 21 µg.kg^?1 upon 15 kGy irradiation at a dose rate of 8.49 kGy h^?1. The total bacterial load was reduced from 2.4 to < 1 log₁₀ cfu g^?1, while wheat chemical properties were not affected.     

Comparative studies of liver and brain glycogen content of male and female Clarias batrachus (L.) after exposure of different doses of arsenic

Different doses of arsenic (As) were used to investigate comparative toxicity on the liver and brain glycogen content on male and female Indian catfish Clarias batrachus (L.). As-induced effects were associated with gender, dose (5, 10, or 15?mg?L^?1), and varying time periods (48, 96, or 144?h). It was noted that As produced dose- and time-dependent liver glycogenolysis and late brain glycogenolysis. Liver glycogenolysis was significantly increased after 48?h at all three As doses. At the highest dose 15?mg?L^?1, liver glycogen were markedly diminished at in both male and female fish, but in females more reduction was observed than in males. However, with brain glycogen, the significant decrease was noted at 144?h with all three dose levels in both genders, with male being more susceptible. Thus, this study indicates that As produces glycogenolysis. The reduction in the liver glycogen content was more pronounced in female than in the male fish, whereas brain glycogen content decrease was more prominent in males.     

Hepatoprotective and antioxidant effects of Bridelia retusa against carbon tetrachloride-induced hepatotoxicity

The aim of present study was to validate hepatoprotective and antioxidant activities of the bark of Bridelia retusa. The aqueous ethanol extract of B. retusa exhibited highest in vitro hepatoprotective effects as evident from the significantly reduced serum glutamate oxaloacetate transaminase (SGOT) and serum glutamate pyruvate transaminase (SGPT) into the incubation medium of rat hepatocytes with carbon tetrachloride (CCl₄), over the other organic extracts (chloroform, ethylacetate, and methanol). CCl₄ administered through subcutaneous injection produced a marked elevation in the serum levels of GOT, GPT, lactate dehydrogenase, alkaline phosphatase, bilirubin, thiobarbituric acid reactive substances, and decreased in the levels of reduced glutathione, superoxide dismutase, catalase, glutathione-S-transferase, glutathione reductase, glutathione peroxidase, and total protein content. The biochemical activities were normalized in the pretreatment of rats induced by CCl₄ with different doses (250 and 500 mg kg^?1) of the aqueous ethanol extract of B. retusa. Histopathological changes induced by CCl₄ were also significantly attenuated by aqueous ethanol extract of B. retusa treatment. The activity of the aqueous ethanol extract of B. retusa at the dose of 500 mg kg^?1 was comparable to the standard drug, silymarin (25 mg kg^?1). The overall data indicated that B. retusa possesses a potent protective effect against CCl₄-induced hepatic damage and oxidative stress.     

Distribution of mercury in the sediments of some freshwater bodies in Ethiopia

Sediment samples were collected from Tinishu Akaki River (TAR), Lake Awassa, and Lake Ziway, Ethiopia for determination of mercury. The air-dried samples were analyzed for mercury with a differential atomic absorption spectrometer after thermal evaporation of bound mercury converting it to its atomic form. Certified reference materials (CRMs) of sediments and soils were used to validate the method. The recovery of mercury from CRMs and sediments was in the range of 95–100%. The limit of detection for the determination of mercury was 50?ng?kg^?1. The concentration of total mercury in the sediments varied from 3.9 to 110?µg?kg^?1 for TAR, 14 to 67?µg?kg^?1 for Lake Awassa, and 17 to 110?µg?kg^?1 for Lake Ziway. It was found that the total mercury concentrations in all samples were below the United States Environmental Protection Agency guideline of 200?µg?kg^?1.     

Repeated-dose toxicity attributed to aluminum nanoparticles following 28-day oral administration,particularly on gene expression in mouse brain

Nanotechnology is a rapidly growing industry that has elicited much concern due to the lack of available toxicity data. Aluminum oxide nanoparticles (AlNP) were listed as a high-priority group in the Organization for Economic Co-operation and Development (OECD) Steering Group for Test Guidelines. In this study, AlNP 35 ± 18.8 nm in size were administered daily at doses of 15, 30, or 60 mg k^?1 for 28 days. A significant decrease in white blood cells (WBC), neutrophils, lymphocytes, and monocytes was observed in the group treated with 60 mg kg^?1 of AlNP, accompanied by a significant increase in platelets. The concentration of aluminum (Al) rose significantly in the thymus, lung, and brain of the group treated with 60 mg kg^?1 of AlNP. However, no significant changes in histopathology were observed. The expression for feeding behavior, energy expenditure, and neurodegeneration-related genes were up-regulated more than twofold by 60 mg kg^?1 AlNP. Consequently, data suggest that exposure to AlNP may result in adverse health effects, including but not limited to growth inhibition, immunosuppression, and neurodegeneration.