Thanks to research over the past 15 years or so, we now know that
the bitter taste receptors in our mouths release neurotransmitters that stimulate, via the vagus nerve, an increase in intracellular calcium concentrations.
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.
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).
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.
Not exact matches
Researchers were surprised to find
receptors for
bitter taste in the lungs, and more surprised that activating them caused airways to greatly relax.
«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.
Like its human counterpart, the cat
bitter taste receptor Tas2r43 was activated by
bitter compounds aloin (found
in the aloe plant) and denatonium (used to deter children and pets from consuming chemicals such as antifreeze) but responded differently to the compounds.
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.
«Variation
in bitter receptor mRNA expression affects
taste perception.»
«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.&raqu
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.&raqu
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
In most animals,
taste has evolved to avoid all things
bitter — a key to survival — to avoid eating something that could be poisonous via
taste receptors, known as Tas2r, that quickly spring into action and elicit the
bitter sensation.
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.
In previous studies, other gustatory
receptors have been found to allow insects to smell carbon dioxide and to
taste sugar and
bitter chemicals like caffeine.
AMP has no bitterness of its own, but when put
in foods, Margolskee and his colleagues discovered, it attaches to
bitter -
taste receptors.
Researchers start by coaxing cells
in culture to activate
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.&raqu
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.&raqu
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.»
Numerous small differences
in taste receptor DNA sequences affect whether people perceive the
bitter ingredients
in a gin and tonic as intense or mild.
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.
All you need to do is stimulate the
taste receptors for
bitter flavor
in experimental animals and they show a four - hour decrease
in consumption after a meal.
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.