Parkinson's
PCBs, fungicide make brain cells vulnerable for Parkinson's
By Pankaj, US Correspondent
Feb 10, 2005, 17:48

University of Rochester scientists investigating the link between PCBs, pesticides and Parkinson's disease demonstrated new and intricate reactions that occur in certain brain cells, making them more vulnerable to injury after exposures.

In two papers published in the journal NeuroToxicology (Dec. 2004 and Feb. 2005), the group describes how polychlorinated biphenyls (PCBs) disrupt dopamine neurons, which are the cells that degenerate during the course of Parkinson's disease. Researchers also show that low levels of maneb, a fungicide commonly used in farming, can injure the antioxidant system in those same types of cells. Environmental contaminants might make dopamine cells more vulnerable to damage from normal aging, infection, or subsequent exposure to pollutants, researchers say.

The investigation is part of a nationwide race to better understand every aspect of Parkinson's disease, which affects up to 1 million Americans. It is a progressive neurological disorder that occurs when certain nerve cells in the substantia nigra region of the brain die or can no longer produce the brain chemical dopamine. A lack of dopamine is what causes patients to experience tremors, stiffness in the limbs and trunk, and impaired movement or balance.

In the 1990s scientists reported that the brains of Parkinson's patients contained elevated levels of PCBs and certain pesticides. While researchers believe that genetics, the aging process and exposure to toxicants all play a role in the development of Parkinson's, the group led by Lisa Opanashuk, Ph.D., is focused on environmental exposures. The National Institute of Environmental Health Sciences is funding the work.

"If we can identify the mechanisms by which PCBs or pesticides perturb dopamine neuron function, it may lead to the development of therapies that can prevent, slow or stop the progression of Parkinson's," says Opanashuk, an assistant professor of Environmental Medicine.

PCBs create havoc in the body's cellular system by producing free radicals, which leads to a process known as oxidative stress (OS). Oxidative stress is thought to be one of the main causes of cell degeneration. Normally, antioxidants can balance the damage done by OS. But toxic pesticide exposure, combined with the normal aging process, shifts the equilibrium toward oxidative stress and neurodegeneration.

The Rochester studies demonstrate, for the first time, the intricate OS and antioxidant responses to PCBs in dopamine neurons. Investigators treated dopamine cells and other brain cells with PCBs and documented the activation of oxidative-stress related pathways. Further research will evaluate how PCBs become risk factors for disease.

PCBs, used as industrial coolants and lubricants, were banned in 1977 but remain widespread in the environment due to their improper disposal. They linger in the food chain, particularly in wild and farmed salmon and other fish. PCBs accumulate in the body in fat and brain cells and other tissues. The potential adverse health effects of PCBs are dependent upon many factors, such as the levels of exposure, the toxicities of individual chemicals present in any given mixture, and their interactive properties.

Pesticides such as maneb remain in farmed soil for 20-75 days following application and can be found on produce for more than three weeks, even after washing, according to researchers. Until now, the effect of maneb on oxidative stress responses in dopamine neurons was unknown.

But Opanashuk's group shows that just as in exposure to PCBs, cells treated with low levels of maneb also undergo changes that disturb the balance in the antioxidant defense system. Another concern is whether maneb causes more damage when people are exposed in combination with other pesticides, which occurs in rural communities. Opanashuk hopes the research will lead to developing safety guidelines and determining more closely the role that maneb plays in neurological diseases.

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