qwe said:take that all u krazy bitches that tell me pot sucks and alcohol has been proven healthy to the heart!
hell yes LSD is next

then i will truly know my heart will be in good shape well into my old age

qwe said:take that all u krazy bitches that tell me pot sucks and alcohol has been proven healthy to the heart!
why didnt the mice experience this same "stress response"
I know at least a few people with coronory artery disease. They tell them its OK to drink coffee (moderately) if they want and an excersise program (approached moderately) is one of the most important lifestyle changes one can make to combat the disease and is strongly recommended. There is no strong evidence moderate caffeine use increases a persons risk of heart disease or heart attack. With heavy use, however, the evidence is more convincing.
Translation: business and anti-drug establishment interests, the same interests you seem to represent.
Oh come on... use some common sense. Sure, there's a pharmaceutical and financial agenda to this, but the study is only stating a fairly obvious fact.gloggawogga said:Of course...pot is only good for you when distributed in some patented form by a profit making pharmecuetical company...
I didn't know I represented any interests, especially anti-drug ones.
MDApleeze said:its called a vaporizer. GET ONE NOW.
But scientists warn that simply smoking cannabis does not offer the same benefit and may actually damage the heart.
The findings by Steffens et al. are striking, but they should not be taken to mean that smoking marijuana is beneficial for the heart. The dose-response curve to THC in this study was very narrow and U-shaped, with higher and lower concentrations failing to produce protective effects. It would be difficult to achieve such specific concentrations in the blood by smoking marijuana. Also, no studies have been performed in humans to evaluate the effects of THC on atherosclerosis. As the authors note, the ApoE-/- mice develop extremely high levels of serum lipids, and THC, which is very fat-soluble, is likely to be stored at high local concentrations within atherosclerotic lesions7. Whether this local storage occurs, and whether the same effect will occur in human atherosclerotic lesions, remains to be determined.
Finally, THC binds to and activates CB1 and CB2 receptors with similar affinity. Marijuana smoking, acting through its effect on CB1 receptors in the brain, increases the pulse rate, produces an acute rise in blood pressure and then results in sudden falls in blood pressure upon standing or walking (Fig. 1). These effects lower the exercise threshold for angina, and are an independent risk factor for heart attack and stroke8, 9. When inhaled, marijuana smoke also increases the concentration of carboxy-haemoglobin in the blood, impairing oxygen delivery. Ultimately, to take advantage of the positive effects reported by Steffens et al. will probably mean developing cannabinoids that target CB2 receptors, rather than using marijuana or oral THC as medicines.