Health & Wellbeing

Sugar is the key to the nicotine rush according to new research

Sugar is the key to the nicotine rush according to new research
USC College associate professor Lin Chen, left, and Keck School associate professor Zuo-Zhong Wang worked on the nicotine study with research associate Cosma Dellisanti,
USC College associate professor Lin Chen, left, and Keck School associate professor Zuo-Zhong Wang worked on the nicotine study with research associate Cosma Dellisanti,
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USC College associate professor Lin Chen, left, and Keck School associate professor Zuo-Zhong Wang worked on the nicotine study with research associate Cosma Dellisanti,
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USC College associate professor Lin Chen, left, and Keck School associate professor Zuo-Zhong Wang worked on the nicotine study with research associate Cosma Dellisanti,

July 27, 2007 Smoking and blood sugar levels are highly interrelated – nicotine causes the body to release satisfying levels of sugar into the bloodstream far faster than eating can, which explains its appetite-inhibiting effects. The results of low blood sugar levels in a quitting nicotine addict are also responsible for some of the most difficult withdrawal symptoms. Now it has been discovered that sugar is also a key element in the chemical reaction that causes a smoker to feel “high”. When nicotine molecules are received by neurotransmitter membranes, it’s sugar molecules that then act as a sort of hinge to open a gate in the cell membrane and send the "nicotine rush" nerve signal onward.

When nicotine binds to a neuron, how does the cell know to send the signal that announces a smoker’s "high"? As with other questions involving good sensations, the answer appears to be sugar.

A USC study appearing with a commentary in Nature Neuroscience online proposes a role for sugar as the hinge that opens a gate in the cell membrane and brings news of nicotine’s arrival.

Structural biologist Raymond Stevens of The Scripps Research Institute, who was not involved in the study, called it “a landmark accomplishment for the fields of structural biology and neuronal cell signaling.”

Besides substance addiction, Stevens pointed to epilepsy, schizophrenia and depression as targets for improved drugs that could result from the study’s findings.

The study provides the first detailed look at part of the mouse nicotinic acetylcholine receptor (nAChR), one in a large and important group of molecules, known as ion channel proteins, that allow signals to pass between neurons.

The results reveal an important role for the sugar molecules in such proteins.

“Our studies fill a major gap in the field and set a new paradigm,” said Lin Chen, associate professor of molecular and computational biology in USC College and co-corresponding author with Zuo-Zhong Wang, associate professor of cell and neurobiology at the Keck School of Medicine of USC.

Many existing theories, which do not consider sugar’s role, are probably incomplete, Chen said.

The debate over how signals pass from the outside of a cell to the inside is a long-standing one.

Some researchers had suggested that when a chemical such as nicotine binds to an ion channel protein on the cell surface, the protein starts a “conformational wave” that propagates a signal through the protein body to the cell membrane, Chen said.

But the molecular basis of such a wave in nAChR or any other protein has not been clearly established.

Instead, the Chen and Wang groups’ study of crystal structure suggested a simple mechanical role for sugar molecules attached to the surface of the receptor.

“They serve as the link between the neurotransmitter binding site and the membrane region where the gate is located,” Chen said.

“The sugar is kind of like a hinge. It’s pulling the door open and closed.”

Cutting the sugar chains stopped the gate’s operation: “The sugar is critical, in my opinion”, said Chen.

The researchers also found a water molecule deep in the receptor’s core – significant because proteins normally are filled with hydrophobic (water repellent) matter that helps the structure hold its shape according to Chen.

The water molecule may enable the receptor to alter its shape in counterbalance to the bending hinge.

Previously studied “homologs” of nAChR – proteins that share its structure but not its signaling function – are entirely hydrophobic, Chen said, supporting the theory that the buried water molecule plays a functional role.

Chen called the group’s Nature Neuroscience study “one of the few times that you felt that you connected the dots.”

The study also represents a tour de force of protein crystallography. Homologs of nAChR had been studied at the atomic scale, but not the receptor itself. One problem, solved by Wang’s laboratory, was the challenge of isolating large quantities of the nAChR protein in a suitable form.

“Many prestigious institutions and laboratories in the world have experienced tremendous difficulties for over two decades in getting a protein sample amenable for high-resolution studies of the structure,” Wang said.

Cosma Dellisanti, research associate in molecular and computational biology at USC, was first author. The other co-authors were Yun Yao of the Keck School and James Stroud of UCLA.

Funding for the research came from the Muscular Dystrophy Association and the National Institutes of Health.

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