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| Thanks to the following for materials & support |
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Toxicology & Environment
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Environmentally based chemical toxicity is becoming an increasingly prevalent problem in industrial and post-industrial societies. Many chemicals used in both a production capacity or from the food industry have accumulated in the environment or food chain to toxic levels. Understanding the action of what are frequently xenobiotic substances is a challenge.
One path of action for xenobiotics is through existing cellular processes, such as membrane transport phenomena or biochemical pathways. Technologies developed or available through the BRC integrated platforms target many of these processes. For this reason the BRC has established a Toxicology Research Module, coordinated by J. Laskin of Rutgers University to bring these technologies to bear on environmental health issues.
As part of our activities in reproductive health, we demonstrated the inhibition of the V-type proton pump (ATPase) by the metal cadmium. This toxin is known to occur in tobacco and to be a product of aluminum smelting. In both cases, exposure to these environments is known to reduce male fertility.
Although much current emphasis is on relatively recent toxic environmental changes, some sites of pollution go back hundreds to thousands of years. Acidic rivers are good examples, frequently arising near sites of human activity. The BRC, in collaboration with the MBL Bay Paul Center for Molecular Evolution and funded by NSF and NASA, completed a study on the method of survival of the abundant protist life forms present in these extreme acidic conditions. The river in our study area, the Rio Tinto, has a pH of 1-2. The organisms had a near normal cytolsolic pH, around 6.5. We found that their ability to maintain this neutral pH was due to a combination of a positive membrane potential, reversing the electric gradient for proton permeability, and a 7% higher energy budget.
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| • Chemical and environmental effects on mammalian skin >> |
| • Glutamate excitotoxicity >> |
| • Bacterial cell-cell signaling & community succession in biofilms >> |
| • Control of mitochondrial function by nitric oxide >> |
| • Role of hypoxia in regulating gene expression >> |
| • Environmental effects on signal >> |
• Adaptations of unicellular eukaryotes to extremely
acidic environments >> |
• Mechanisms of luminal acidification in epidydimas and
vas deference >> |
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| 1) Messerli, M.A., Amaral-Zettler, L.A., Zettler, E., Jung, S.K., Smith, P.J.S., Sogin, M.L. 2005. Life at acidic pH imposes an increased energetic cost for a eukaryotic acidophile. Journal of Experimental Biology, 208:2569-2579. |
| 2) Amaral Zettler L.A., Messerli, M.A., Laatsch, A.D., Smith, P.J.S and Sogin M.L. 2003. From Genes to Genomes: Beyond Biodiversity in Spain's Rio Tinto. Biological Bulletin, 204(2): 205-9. |
| 3) Porterfield, D.M., Laskin, J.D., Jung, S.-K., Malchow, R.P., Billack, B., P.J.S. Smith and Heck, D.E. 2001. Proteins and lipids define the diffusional field of nitric oxide. American Journal of Physiology, 281(4): L904-912. |
| 4) Billack, B., Heck, D.E., Porterfield, D.M., Malchow, R.P., Smith, P.J.S., Gardner, C.R., Laskin, D.L. and Laskin, J.D. 2001. Minimal amidine structure for inhibition of nitric oxide biosynthesis. Biochemical Pharmacology, 61(12): 1581-6. |
| 5) Herak-Kramberger, C., Sabolic, I., Blanusa, M., Smith, P.J.S., Brown, D. and Breton, S. 2000. Cadmium inhibits vacuolar H+ATPase-mediated acidification in rat epididymis. Biology of Reproduction. 63: 599-606. |
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