Behrens and his colleagues Kristina Blank and Wolfgang Meyerhof developed a way to screen which
of the bitter taste receptors that saccharin and cyclamate were hitting, to figure out why the combination is more palatable than either one alone.
Not exact matches
Because scientists have discovered that the same
receptors that exist on the tongue to
taste bitter substances are also found on the smooth muscle
of the lungs.
«But as the bacteria multiply, they consume more glucose, removing the sweet
taste receptor «brake» and allowing for release
of AMPs by the
bitter taste receptors.»
«We believe that the complimentary roles
of the
bitter and sweet
taste receptors in these SCCs keeps upper airway colonizing bacteria at optimal levels during periods
of relative health,» Cohen says.
What's more, the action
of the
bitter receptors is blocked when sweet
taste receptors are stimulated by sugars such as glucose.
Now, scientists from the Perelman School
of Medicine at the University
of Pennsylvania reveal that the release
of AMPs is partially controlled by
bitter taste receptors in the upper airway on a cell previously identified in animals and only recently in humans known as solitary chemosensory cells (SCCs).
The teams at AFB International and Integral Molecular studied the behavior
of two different cat
bitter taste receptors in cell - based experiments, investigating their responsiveness to
bitter compounds, and comparing these to the human versions
of these
receptors.
The team also found that probenecid, a known inhibitor
of human
bitter taste receptors, also worked on both cat
taste receptors, preventing stimulation when in the presence
of PTC, aloin and denatonium.
TAS2R38 is a
bitter taste receptor in humans
of which some people have «supertaster» variants that give them an extreme sensitivity to
bitter compounds, explaining some people's strong aversions to broccoli and brussels sprouts.
«Here we show that the bitterness
of sampled ethanol varies with genetic differences in
bitter taste receptor genes, which suggests a likely mechanism to explain previously reported relationships between these gene variants and alcohol intake.»
In the first study to show that the sensations from sampled alcohol vary as a function
of genetics, researchers focused on three chemosensory genes — two
bitter -
taste receptor genes known as TAS2R13 and TAS2R38 and a burn
receptor gene, TRPV1.
«In our research, we show that when people
taste alcohol in the laboratory, the amount
of bitterness they experience differs, and these differences are related to which version
of a
bitter receptor gene the individual has.»
a) The Eye in your Thigh: a patch
of skin cells on the leg that can distinguish between bright and dark conditions, perhaps to help regulate the body clock b) The Ear in your Rear: nerves in the buttocks attuned to infrasound vibrations
of between 10 and 25 hertz, perhaps to warn
of approaching predators or thunderstorms c) The Nose in your Toes: scent - detecting sebaceous glands on the feet whose purpose is unclear d) The Tongue in your Lung:
taste - bud - like
receptors that detect
bitter substances and dilate or restrict the airways accordingly
al., tested the hypothesis that herbivores — and their plant diets — have evolved to have greater number
of Tas2r
bitter taste receptor genes in their genomes than omnivores or carnivores.
Unlike sweet
taste, which has only one or perhaps two different
receptor types, the number
of functional
bitter taste receptor types — those that are able to respond to
bitter compounds — varies greatly across species.
To do this, they incorporated the gene sequence
of each
receptor into cultured cells and then probed the cells to determine if they were activated by one or more
of 25 different
bitter -
tasting chemicals.
AMP has no bitterness
of its own, but when put in foods, Margolskee and his colleagues discovered, it attaches to
bitter -
taste receptors.
As effective as it is, AMP may not be able to dampen every type
of bitter taste, because it probably doesn't attach to all 30
bitter -
taste receptors.
In 2000 Zuker and others found some 30 different kinds
of genes that code for
bitter -
taste receptors.
«In our research, we show that when people
taste alcohol in the laboratory, the amount
of bitterness they experience differs, and these differences are related to which variant
of a
bitter receptor gene the individual has.»
They first discovered that a
bitter taste receptor known as T2R38 plays a role in people's susceptibility to an infection known as chronic rhinosinusitis (CRS)-- a disease that affects nearly 35 million Americans and is a huge driver
of drug resistance.
Blends
of non-caloric sweeteners saccharin and cyclamate show reduced off -
taste due to TAS2R
bitter receptor inhibition.
In our GI tract,
bitter taste receptors can simultaneously promote the absorption
of «safe»
bitter compounds and the excretion
of toxic ones, thereby preventing overexposure to the many low - grade food - borne toxins we eat every day.
The mechanism by which they stimulate boosted digestive capacity is wondrously simple: the
bitter taste receptors on our tongue and other areas
of the mouth register that a
bitter compound has entered your body.
The book covers everything from tone
of voice (high = playful, low = serious) to the reason
bitter spray won't stop inappropriate chomping (bitterness
receptors are on the back
of dogs» tongues, so they won't
taste it on a shoe).