<!--[if !supportLists]-->         <!--[endif]-->Boerhaavia diffusa is a weed foundin India. It was found to stop intra-uterine-contraceptive-device(IUCD)-induced bleeding. This herb is also known for its anti-inflammatory andanalgesic properties, which are comparable to those of ibuprofen. It has alsoproved useful as a hematinic.. It is a diuretic, anti-inflammatory, stomachic,laxative, myocardial stimulant, antibacterial and antiviral. It is useful inasthma, anemia, jaundice, ascites, anasarca, scanty urine, internalinflammation and as an antidote for snake venom.

<!--[if !supportLists]-->        <!--[endif]-->Punarnava helps maintain efficientkidney and urinary functions with its diuretic, anti-spasmodic andanti-inflammatory action.

<!--[if !supportLists]-->        <!--[endif]-->Punarnavacontains alkaloids, ß-sitosterol, ursolic acid, Vitamins D, and E. Research indicates Punarnava helps regulate production of polyamine andprostaglandins which are powerful immuno-suppressants produced in theprostate.  These active principals also support and balance the healthyflow of urine by toning smooth muscles located in the urinogenital system andreducing inflammation of the urethra and prostate.  Punarnava is usedthroughout India for treating organ disorders, stimulating liver function, andpromoting blood circulation.  Punarnava also empowers the body'smetabolism to burn fat and calories at a higher rate.   

Boerhaaviadiffusa is an Ayurvedic remedy used traditionally for the treatment
of a number of diseases, including those affecting the gastrointestinal tract.
In the current investigation, a methanol extract obtained from roots of B.
diffusa exhibited a significant spasmolytic activity in the guinea pig ileum,
probably through a direct effect on the smooth muscle. A detailed phytochemical
analysis of this methanol extract led to the isolation of one new (12) and six
known (6/11) rotenoidderivatives. The structure of the new compound was
determined through interpretation of its MS and NMR data. All the isolated
rotenoids were evaluated for their effect on intestinal motility in vitro, and
the results obtained showed unambiguously that they are active spasmolytic
constituents. Preliminary structure/activity relationships for this class of
compounds are suggested.