Up to $545, thanks to more Anonymous, ydnic, i_descend, liamstliam, and talix18! If I have not thanked you by name and you thought you told the site to use your name, it did not. This has happened to at least one person. Tell me who you are! :) EDIT: And enderfem!
And please, please, sponsor me!
hughcasey is hosting a thread over here...
Disney Princess Strike Force!
I love headlines like this: "Shrek 3 Casts Ninja Princesses".
Got BPAL from cissa! Also got sartorias's Crown Duel!
Oh, this one's superinteresting. Unsuspected Brain Cells May Cause Epilepsy.
The roots of epilepsy lie in an often-overlooked type of brain cell and not in the neurons as was previously thought, a new study claims. The US-based researchers hope their findings will lead to more appropriate treatments for the condition.
Epilepsy is a syndrome that arises when a brain chemical, called glutamate, stimulates neurons to start firing wildly and uncontrollably, sometimes resulting in seizures or loss of consciousness. Current treatments are aimed at slowing down brain function to reduce the neuronal firing, but these have unwelcome side effects, such as drowsiness.
Neurologists generally believe that epilepsy causes the production of abnormal cells called reactive astrocytes – oversized, bloated, star-shaped cells that no longer function properly in their “housekeeping” role of maintaining the brain’s optimum chemical environment.
So Maiken Nedergaard, at the University of Rochester Medical Center, New York, and colleagues decided to take a closer look at the role of astrocytes in epilepsy. The team induced epilepsy in rats using five different known methods, for example lowering the level of brain calcium. They then blocked synaptic activity completely using the neurotoxin tetrodotoxin (TTX), which meant there was no neural firing and therefore no seizures in the rats.
“To our great surprise, we found that there was an increase in reactive astrocytes in all five models, which could not have been caused by over-firing of the neurons as expected – because there had been no neural firing,” says Nedergaard.
“And the reactive astrocytes were producing excessive glutamate in the rats. It turns out that reactive astrocytes trigger epilepsy, and not the other way around,” she concludes.
Astrocytes are a major type of brain cell, but because they are not involved in electrical activity within the brain, they have been studied relatively little.
Donald Weave, president of Epilepsy Canada, agrees. The role of glial cells, the cells that surround and support neurons, in epilepsy and neurology "has been understudied", he says. "We have been hammering away at the same old approaches for years and so a new way in with astrocyte involvement would be very useful."
The cell type is found in larger proportion - and with more “points” on the star-shaped cell - in animals with higher brain function. Monkeys have roughly the same number of astrocytes as neurons in their brains, whereas humans have 10 times as many astrocytes as neurons.
Recently, more has been discovered about the importance of these cells and the role they play in diseases, from stroke to Alzheimer’s.
Blood to brain
One of the roles of these “housekeeper” cells is to mop up excess glutamate. But Nedergaard reports that when the cells become abnormal, they appear to produce detrimental amounts of the chemical. “We need to find a treatment that controls the release of glutamate or inhibits reactive astrocytes. At the moment, the drugs that could do this are not able to pass the blood-brain barrier,” she says.
“It’s very important, because right now we are treating children – who are in education and still learning – with drugs that slow down their synaptic activity and brain function, which is very bad,” she told New Scientist.
The researchers used the rat models to analyse three drugs commonly used to treat epilepsy. They found that in addition to slowing neural firing, the drugs reduced the type of chemical signalling that causes astrocytes to release glutamate. “This may be why they work,” Nedergaard suggests.
Ley Sander, at the UK’s National Society for Epilepsy, comments: "This a most interesting study as it suggests that astrocytes may be involved in the initiation and propagation of epileptic discharges. This is, however, based in animal models and it remains to be seen if this is a true reflection of what happens in the human brain at the time of a seizure. If it is, then new avenues for the pharmacological treatment of epilepsy will be opened.”
And a spokesperson from UK-based charity Epilepsy Action, adds: "We welcome any research into epilepsy, particularly research that is related to a cure for epilepsy, as opposed to suppressing seizures."
Journal reference: Nature Medicine (DOI: 10.1038/nm1277)
Libertine: Rosewood and chamomile with bergamot, violet, red sandalwood, primrose and Arabian musk.
In bottle: Chamomile with a hint of violet...
On me: Very chamomile, with a hint of chemical-rose. Strange - I liked this at the Florida meet-and-sniff? I do not like it now.
Undertow: The Dark Side of Water: clean and purifying, yet menacing -- lotus and juniper with a hint of mint. A scent dragged up from the depths to the Stygian shore.
In bottle: The juniper and mint together are *really* strange! They don't smell like separate notes.
On me: This is the ozone-y smell that I don't get from BPAL's ozone note. It's fascinating. It's difficult to describe. It's tremendously weird. And weird is my kink.
Dana O'Shee: Offerings of milk, honey and sweet grains were made to placate these creatures, and it is that the basis of the scent created in their name.
In bottle: Honey, overtaken by grain.
On me: Almond! Almond bad.
Juke Joint: A bawdy, gleefully wicked and unruly scent: Kentucky Bourbon, sugar and a sprig of mint.
In bottle: Alcohol.
On me: ...my skin has just eaten this entirely. Just like Dormouse. Oh, okay, wait, it's coming back...as just a very mild alcohol. Hrm. It seems that their alcohol-type smells only work on me when they're a minor ingredient. (Torture King has bourbon.) Hm, okay, a tiny bit of sugar-mint. But there's no *base* to this. It utterly fails to be interesting on me.