Masturbation calms restless leg syndrome

Too much of it will make you go blind – or so you might have been told. But for some, masturbation might have a real clinical benefit: it can ease restless leg syndrome (RLS). The insight could provide sweet relief for the 7 to 10 per cent of people in the US and Europe who suffer from the condition.
RLS is a distressing neurologic disorder characterised by an urge to move the legs. It is usually associated with unpleasant sensations in the lower limbs such as tingling, aching and itching.
The exact causes of RSL have yet to be pinpointed, but brain autopsies and imaging studies suggest one contributing factor is an imbalance of dopamine – a hormonal messenger that, among other things, activates the areas of the brain responsible for pleasure. It is suspected that dopamine imbalance is responsible for some of the symptoms of Parkinson's disease.
Drugs that increase dopamine have been shown to reduce symptoms of RLS when taken at bedtime and are considered the initial treatment of choice.
Although such drugs provided significant improvement of symptoms for a 41-year-old man with RLS, he found an even better treatment – complete relief after masturbation or sex.

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Cannabis-like drugs could kill pain without the high

An ingenious set of experiments has teased apart the mind-altering and pain-relieving effects of the main component of cannabis. This could open the way to cannabis-like drugs that provide pain relief without causing unwanted highs.

Cannabis is taken as a painkiller – to dull pain in cancer for example – but it can produce unpleasant side effects such as hallucinations and impaired mobility.

Now, a team led by Li Zhang of the US National Institute on Alcohol Abuse and Alcoholism in Bethesda, Maryland, has shown that tetrahydrocannabinol (THC) – the active component in cannabis that makes people high but that is also thought to dull pain – binds to different molecular targets on cells to produce these two effects.

It has long been known that THC gives people a high by binding to a molecular anchor on cells called the cannabinoid type-1 (CB1) receptor. Zhang and his team discovered that THC relieves pain by binding instead to receptors for the brain-signalling compound glycine and increasing their activity.

Through experiments on mice, they then confirmed that if the glycine receptor is absent or if its activity is blocked by another drug, the animals experienced pain in a standard "tail-flick" test even when given THC, confirming that the drug's pain-relief and psychotropic effects can be decoupled.

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