Evaluation of developmental toxicity and apoptotic induction of the aqueous extract of Millettia pachycarpa using zebrafish as model organism

Extensive and indiscriminate use of synthetic compounds and natural compounds obtained from plant sources have resulted in serious threats to the aquatic ecosystem and human health. Aqueous extract of the root of the plant, Milletia pachycarpa Benth, is currently used for killing fish in the state of Manipur, India. Moreover, this plant is also used as traditional medicine in this region. Although it is widely used in traditional medicine, there is limited information available regarding the adverse effects and mechanism underlying its toxicity. This study examined the effects of exposure to aqueous extract of M. pachycarpa (AEMP) on early embryonic development of zebrafish embryos and mechanisms underlying toxicity. Zebrafish embryos treated with different concentrations of the AEMP produced embryonic lethality and developmental defects. The 96-hr-LC₅₀ of AEMP was found to be 4.276 µg/mL. Further, multiple developmental abnormalities such as pericardial edema, yolk sac edema, spinal curvature, swim bladder deflation, decreased heart rate, and delayed hatching were also observed in a dose-dependent manner. Zebrafish embryo showing moderate-to-severe developmental defects following AEMP exposure cannot swim properly. Further, this study examined oxidative stress and apoptosis in embryos exposed to AEMP. Enhanced production of ROS and apoptosis was found in brain, trunk, and tail of zebrafish embryos treated with AEMP. Data suggest that oxidative stress and apoptosis are associated with AEMP-induced embryonic lethality and developmental toxicity in zebrafish embryos.     

Toxicity evaluation of 10 oil gelling agents北大核心CSCD

Oil gelling agents are widely used in emergency response of marine oil spills. However, the biological toxicity of oil gelling agents is not well understood. This research aimed to evaluate the environmental safety of oil gelling agents used for rapid removal and cleanup of marine oil spills. We used luminescent bacteria (Acinetobacter sp. Tox2 and Acinetobacter sp. RecA) combined with exposure experiment using marine medaka (Oryzias melastigma) juveniles to detect the acute toxicity and genotoxicity of 10 oil gelling agents. As a result, a certain level of acute toxicity was detected from the oil gelling agent FOA and GMN-01 (the toxicity equivalent to 0.067 mg/L and 0.084 mg/L of HgCl2, respectively), and a certain level of genotoxicity was detected from the oil gelling agent NORSOREX (the toxicity equivalent to 0.307 mg/L of MMC) by the luminescent bacteria test. However, no obvious acute toxicity or genotoxicity was detected from the above three oil gelling agents in fish-exposure experiments. Our results suggest that the 10 oil gelling agents have no obvious acute toxicity or genotoxicity to higher organisms (including marine medaka). The luminescent bacteria test is more sensitive in detecting biological toxicity of oil gelling agents. This study provides a reference for environmental safety evaluation of the oil gelling agents used in the cleaning up of the marine oil spills.     

Washing out heavy metals from contaminated soils from an iron and steel smelting site

Washing is a promising method for separating contaminants bound to the particles of soil ex-situ by chemical mobilization. Laboratory batch washing experiments were conducted using deionized water and varying concentrations of oxalic acid, citric acid, tartaric acid, acetic acid, hydrochloric acid and ethylenediaminetetra acetic acid (EDTA) to assess the efficiency of using these chemicals as washing agents and to clean up heavy metals from two heavily polluted soils from an iron and streel smelting site. The toxicity reduction index and remediation costs were analyzed, and the results showed that the soils were polluted with Cd, Pb and Zn. Hydrochloric acid and EDTA were more efficient than the other washing agents in the remediation of the test soils. The maximum total toxicity reduction index showed that 0.5 mol·L^-1 hydrochloric acid could achieve the remediation with the lowest costs.     

Oxidative stress and changes in locomotor behavior and gill morphology of Gambusia affinis exposed to chromium

Sublethal effects of chromium trioxide on mosquito fish, Gambusia affinis, were carried out for 28 days on day 4, 8, 12, 16, 20, 24, and 28. The sublethal effects of chromium (LC₁₀, 77.62?mg?L^?1) on antioxidant enzymes, thiobarbituric acid reactive substance (TBARS), locomotor behavior, and gill morphology were studied. The antioxidant enzymes like superoxide dismutase (SOD) and catalase were induced throughout the exposure span of 28 days. Percent induction was also increase with the days of exposure. Lipid peroxidation product, malondialdehyde was enhanced in the viscera tissue of chromium-exposed fish. Perturbation of locomotor behavior like decrease in distance travelled (m?min^?1) and in swimming speed (cm?s^?1) was observed in exposed fish. Chromium toxicity caused alterations in gill morphology like hypertrophy and hyperplasia in secondary lamellae followed by detached epithelium with severe necrosis. It can be concluded from the results that Cr intoxication in Gambusia fish, caused induction in antioxidant enzymes and lipid peroxidation, plus changes in gill morphology and locomotor behavior.     

Comparative sensitivities of the tropical cladoceran,Ceriodaphnia rigaudii and the temperate species Daphnia magna to seven toxicants

The toxicities of seven chemicals [cadmium (Cd) chloride, potassium dichromate, sodium dodecyl sulfate, potassium chloride (KCl), Triton X-100, zinc (Zn) chloride and copper (Cu) (II) sulfate] were determined using the tropical freshwater cladoceran, Ceriodaphnia rigaudii and the temperate species, Daphnia magna. Data generated was subsequently used to determine the relative sensitivities of both species, using interspecies correlation to compare the 48?h LC50 values for both species. The 48?h LC50 values for C. rigaudii ranged from 0.002?mg?L^?1 (potassium dichromate) to 21.1?mg?L^?1 (KCl), whereas those for D. magna ranged from 0.3?mg?L^?1 for Cu to 418.87?mg?L^?1 for KCl. The LC50 values for C. rigaudii were significantly less than that for D. magna for six of the compounds tested. The interspecies correlation also showed a low, positive correlation suggesting that the sensitivities of both species were not similar for the compounds tested. The sensitivity factors for C. rigaudii and D. magna ranged between 0.01 and 12.3. These values further suggested that for six of the compounds tested, C. rigaudii appeared to be more sensitive than D. magna. It is therefore possible that because of these differences in relative sensitivities, toxicity data generated with D. magna may not be appropriate for Trinidad.     

Amelioration of fluoride toxicity by vitamins and calcium on reproductive organs of female rat

Normal female rats of Wistar strain (Rattus norvegicus) weighing between 150–200 g were treated with fluoride (Fl) contaminated drinking water (FW, 5.8 ppm), vitamin C (6 mg) and vitamin C (6 mg) + D (6 mg once a week) + calcium (6 mg) for 30 days. Fl water treatment to rats produced reduction in weights of ovaries, uterus, vagina, kidneys, and adrenal glands, circulating levels of estrogen, number of litters, fertility rate, and altered tissue and serum biochemistry compared to control rats. However, cholesterol concentrations of ovaries and adrenals increased significantly. The above altered parameters were restored partially/completely after exogenous feeding with vitamin C and vitamins (C + D) and calcium. The data suggest that Fl-induced adverse effects on reproductive and other organs in female rats, whereas vitamin C, vitamin D and calcium treatment ameliorated Fl toxicity. Therefore, vitamins (C and D) and calcium play an important role in prophylactic treatment of fluorosis.     

Effects of coconut product–caffeine interactions on liver cells in Wistar albino rats

The effects of interactions between coconut products and caffeine on the induction of drug-metabolizing enzyme in Wistar albino rats were studied. Twenty rats were randomly divided into four groups: (Group 1) control received via oral route a placebo (4 mL distilled water). Groups 2–4 were treated for a 14-day period, respectively, with 50 mg caffeine/kg body weight (BW), 50 mg caffeine/kg plus 50 mg coconut water/kg, or 50 mg caffeine/kg plus 50 mg coconut milk/kg in a 4 mL volume via gastric intubation. One day after the after the final exposure, the animals were euthanized by inhalation of an overdose of chloroform. The blood of each rat was collected by cardiac puncture, and the liver of each was harvested and processed to examine several biochemical parameters, including total protein and RNA levels, protein/RNA ratios, and the activities of alanine and aspartate aminotransferases (ALT and AST, respectively). Results showed that while ingestion of coconut milk and coconut water increased the values of protein and protein/RNA ratios, there was a decrease in ALT and AST activities. These effects were opposite to those produced by caffeine alone and may prevent the adverse effects attributed to caffeine.     

An approach for assessing the suitability of Ceriodaphnia rigaudii as an indigenous tropical toxicity test species

Although the selection criteria for toxicity test species are well-documented, they do not provide a clear approach for establishing the suitability of a species for regulatory testing. This study looks at the approach used to determine if Ceriodaphnia rigaudii, an indigenous tropical cladoceran species, may be designated as a suitable freshwater test species for regulatory testing in Trinidad and Tobago. The approach involved species identification, life cycle characterization, salinity tolerance, toxicological responses to standard chemicals, and comparative sensitivity evaluation with an established test species. The results showed that C. rigaudii (0.45 mm) was significantly smaller in size, had a shorter life cycle and matured faster than temperate cladoceran species such as Ceriodaphnia dubia and Daphnia magna (3–6 mm). Ceriodaphnia rigaudii has a life span of about 10–15 days and reached sexual maturity within 2 days, whereas D. magna had a life span of about 40–50 days and attained sexual maturity within 6–10 days. The LC₅₀ values for C. rigaudii were significantly less than D. magna for the six compounds tested. Interspecies correlation also showed a low positive correlation, suggesting that the sensitivities of both species were not similar for the compounds tested. The sensitivity factors of C. rigaudii and D. magna for the toxicants ranged 0.01–12.3, suggesting that C. rigaudii was more sensitive than D. magna. This study was useful in defining a stepwise approach to help establish C. rigaudii as an indigenous tropical toxicity test species in Trinidad.     

Histological and histochemical alterations induced by lead in the liver of the quail Coturnix coturnix

Adult males of the quail Coturnix coturnix were exposed to lead acetate trihydrate in drinking water (0.1, 0.25, 0.5, and 1% for one–six months) to investigate histological and histochemical alterations induced by lead intoxication in the liver. Chronic exposure to subtoxic concentrations of lead produced changes in hepatocytes, portal veins, Kupffer cells, and blood sinusoids. Alterations in hepatocytes mainly involved cytoplasmic vacuolation, necrosis, cytolysis, and glycogen accumulation. Kupffer cell hyperplasia, hemosiderosis, blood sinusoidal dilatation, portal vein congestion, and edema were also observed. No fibrosis or cirrhosis in the liver of any member of the dose groups over the entire period of the study was noted. The findings revealed that chronic exposure to lead produced mild histological and histochemical changes in the liver of the quail Coturnix coturnix.     

Purification,characterization and toxicity of a mannose-binding lectin from the seeds of Treculia africana plant

In this study, a mannose-specific, homodimeric lectin from the seeds of Treculia africana was purified, characterized and its adverse effects were investigated in mice. The purification protocol involved anionic exchange chromatography on DEAE-Cellulose followed by gel filtration on Sephadex G-100. The hemagglutinating activity of lectin towards human erythrocytes was sensitive to inhibition by D-mannose. Treatment of the protein with EDTA exerted no inhibitory effect; however, analysis of metal content by atomic absorption spectroscopy revealed the presence of Cu²⁺, Fe³⁺, and Mg²⁺. The results obtained showed that the lectin possesses maximum hemagglutinating activity towards human erythrocytes activity over the pH range 3–7.2 and is relatively thermostable up to 50°C. Periodic acid Schiff's (PAS) reagent staining showed that the protein was non-glycosylated while its amino acid composition analysis revealed that the protein contained 155 residues per subunit. The subunit had a minimal molecular weight of 22,139 Daltons, while the native molecular weight was estimated to be 41,000 Daltons. The lectin was found to be moderately toxic to mice with an LD₅₀ of 47.21 µg g^?1 body weight while, histopathological analysis showed no treatment related effects in any of the organs examined.