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“We’ve now connected a whole class of antipsychotics to natural
brain chemicals that trigger appetite,” says Solomon H. Snyder, M.D.,
professor of neuroscience at the Johns Hopkins School of Medicine. “Our
identification of the molecular players that link such drugs to increased food
intake means there’s now hope for finding a newer generation of drugs
without the weight-gain side effects.”
.Previous research already had fingered increased levels and actions of one
particular enzyme, AMPK, in brain cells as a control lever for appetite in mice
and presumably humans.
Suspecting that antipsychotic drugs might spike AMPK in the brain to overact,
the Johns Hopkins team injected mice with clozapine (Clozaril), which, with
olanzapine (Zyprexa) and risperidone (Risperdal), is commonly prescribed for
schizophrenia and bipolar disorder in people who do poorly on conventional drugs.
Mice given clozapine showed quadrupled AMPK activity compared to activity
measured pre-drug. The researchers then gave the mice leptin, a hormone that
suppresses appetite, and as suspected, saw lowered AMPK levels.
Drilling down further into what controls AMPK and its boost of hunger, Sangwon
Kim, Ph.D., a research associate and lead author of the study, “rounded
up the usual suspects, brain proteins known to relay communication from cell
to cell.”
Systematically manipulating these cell-signaling proteins, Snyder’s team
found that blocking one in particular, a receptor site for histamine, a well-known
player in triggering classic allergy symptoms, activates AMPK to the same extent
as clozapine. To confirm that the histamine receptor connects the drug, AMPK
activity and appetite, the team gave clozapine to mice genetically engineered
without a histamine receptor. Results? No heightened AMPK activity.
“Histamine also has a long history as a suspect in weight control, but
no one ever could put a finger on the exact link,” says Snyder. “The
connection we’ve made between its receptor and appetite control is incredibly
intriguing and opens new avenues for research on weight control, possibly including
drugs that suppress appetite safely.”
Authors on the paper are Kim, Alex Huang, Adele Snowman and Snyder of Hopkins,
and Cory Teuscher of the University of Vermont College of Medicine. Published
Feb. 20th online at the Proceedings of the National Academy of Sciences. http://neuroscience.jhu.edu/index.php
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FACT:
More Reasons You Should NOT Rely on Bottled Water: German researchers have found
that the longer a bottle of water sits on a store shelf or in a household pantry,
the higher the dose of antimony it contains. Amounts of this potentially toxic
trace element were measured for 15 brands of Canadian bottled water and 48 European
brands. Concentrations reached more than 100 times the average level of antimony
in pristine groundwaters (2 parts per trillion). However, the concentration
was even higher after the bottles were left to sit at room temperature for six
months. Antimony concentrations in the Canadian bottled waters increased by
19 percent, concentrations in the European brands increased by 90 percent. Most
of the water tested was packaged in bottles made of polyethylene terephthalate
(PET). Antimony trioxide is used as a catalyst in the manufacture of PET. The
different concentrations of antimony in the various brands might have been caused
by differing temperatures, water pHs, or exposure to sunlight.
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