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Bromelain extract is a mixture of protein-digesting (proteolytic) enzymes and several other substances in smaller quantities. The proteolytic enzymes are sulfhydryl proteases; a free sulfhydryl group of a cysteine amino acid side chain is required for function.
May worsen hormone sensitive conditions such as breast cancer, uterine cancer, ovarian cancer, endometriosis, and uterine fibroids. [17] Insomnia. [17] Goldenseal: orangeroot, yellow puccoon Hydrastis canadensis: Uterotonic [3] Greater celandine: celandine Chelidonium majus: Liver damage [4] Guarana: Paullinia cupana: Agitation and insomnia [3 ...
The effect was first discovered accidentally in 1989, when a test of drug interactions with alcohol used grapefruit juice to hide the taste of the ethanol. [9] [10] A 2005 medical review advised patients to avoid all citrus juices until further research clarifies the risks. [11]
There can be many years between promising laboratory work and the availability of an effective anti-cancer drug: Monroe Eliot Wall discovered anti-cancer properties in Camptotheca in 1958, but it was not until 1996 – after further research and rounds of clinical trials – that topotecan, a synthetic derivative of a chemical in the plant, was ...
Cancer Research UK states, "there is no evidence to show that the Rife machine does what its supporters say it does". [40] Therapeutic Touch (or TT) – contrary to its name, a technique that does not usually involve touching; rather, a practitioner holds their hands close to a patient to affect the "energy" in their body. According to the ...
Here's why antibiotics are used in the first place—and how they actually impact the human body.
Antibiotic use is common in older people, with those over age 65 consuming 50% more antibiotics than younger adults. Using antibiotics is linked to disturbance of the gut microbiome, which may ...
[2] [85] [86] [87] Research is limited on the effect of this inhibition on iron status. [ 88 ] Metabolism of polyphenols can result in flavonoid-drug interactions, such as in grapefruit–drug interactions , which involves inhibition of the liver enzyme , CYP3A4 , likely by grapefruit furanocoumarins , a class of polyphenol.