<<Gladys it all depends on what you were taking the Noni Juice for.  One
bottle will not tell you a thing>>

  we are a society that is promised "magic pills" by conventional medicine,
and although nthey don't deliver, we have been indoctrinated into thinking
this way so still look fro the "magic pill" in everything we try.

   The benefits of Noni are well-documented. Below are two of nineteen
studies found at PubMed on Noni--Catherine


Ann N Y Acad Sci 2001 Dec;952:161-8

 Cancer preventive effect of Morinda citrifolia (Noni).

Wang MY, Su C.

Department of Pathology, UIC College of Medicine, Rockford, Illinois 61107,
USA. mianw...@uic.edu

Morinda citrifolia (Noni) has been extensively used in folk medicine by
Polynesians for over 2,000 years. It has been reported to have broad
therapeutic effects, including anticancer activity, in both clinical
practice and laboratory animal models. The mechanism for these effects
remains unknown. The hypothesis that Morinda citrifolia possesses a cancer
preventive effect at the initiation stage of carcinogenesis was studied. Our
preliminary data indicated that 10% Tahitian Noni Liquid Dietary Supplement
or Tahitian Noni Juice (TNJ), made from Morinda citrifolia fruit by Morinda
Inc, in drinking water for one week was able to prevent DMBA-DNA adduct
formation. The levels of DMBA-DNA adducts were reduced by 30% in the heart,
41% in the lung, 42% in the liver, and 80% in the kidney of female SD rats.
Even more dramatic results were obtained in male C57 BL-6 mice: 10% TNJ was
able to reduce DMBA-DNA adduct formation by 60% in the heart, 50% in the
lung, 70% in the liver, and 90% in the kidney. In order to explore the
mechanism of this preventive effect, the antioxidant activity of TNJ was
examined in vitro by lipid hydroperoxide (LPO) and tetrazolium nitroblue
(TNB) assays. In the LPO assay, LPO oxidizes leucomethylene blue to
methylene blue in the presence of hemoglobin. The resultant blue color was
quantified at 660 nm spectrophotometrically. In the TNB assay, superoxide
anion radicals (SAR) reduce TNB into formazan blue that was also measured by
absorption at 602 nm. TNJ showed a dose-dependent inhibition of both LPO and
SAR in our system. The antioxidant activity of TNJ was compared to the
effects of vitamin C, grape seed powder (GSP), and pycnogenol (PYC) at the
daily dose per serving level recommended by U.S.RDAs or manufacturers. The
results suggest that prevention of carcinogen-DNA adduct formation and the
antioxidant activity of TNJ may contribute to the cancer preventive effect
of Morinda citrifolia.

PMID: 11795436
________________________________________________________

Phytother Res 1999 Aug;13(5):380-7


An immunomodulatory polysaccharide-rich substance from the fruit juice of
Morinda citrifolia (noni) with antitumour activity.

Hirazumi A, Furusawa E.

Department of Pharmacology, John A., Burns School of Medicine, 1960 East
West Road, University of Hawaii, Honolulu, HI 96822, USA.

The fruit juice of Morinda citrifolia (noni) contains a polysaccharide-rich
substance (noni-ppt) with antitumour activity in the Lewis lung (LLC)
peritoneal carcinomatosis model. Therapeutic administration of noni-ppt
significantly enhanced the duration of survival of inbred syngeneic LLC
tumour bearing mice. It did not exert significant cytotoxic effects in an
adapted culture of LLC cells, LLC1, but could activate peritoneal exudate
cells (PEC) to impart profound toxicity when co-cultured with the tumour
cells. This suggested the possibility that noni-ppt may suppress tumour
growth through activation of the host immune system. Concomitant treatment
with the immunosuppressive agent, 2-chloroadenosine (C1-Ade) or cyclosporin
(cys-A) diminished its activity, thereby substantiating an immunomodulatory
mechanism. Noni-ppt was also capable of stimulating the release of several
mediators from murine effector cells, including tumour necrosis factor-alpha
(TNF-alpha), interleukin-1beta (IL-1beta), IL-10, IL-12 p70,
interferon-gamma (IFN-gamma) and nitric oxide (NO), but had no effect on
IL-2 and suppressed IL-4 release. Improved survival time and curative
effects occurred when noni-ppt was combined with sub-optimal doses of the
standard chemotherapeutic agents, adriamycin (Adria), cisplatin (CDDP),
5-fluorouracil (5-FU), and vincristine (VCR), suggesting important clinical
applications of noni-ppt as a supplemental agent in cancer treatment.
Copyright 1999 John Wiley & Sons, Ltd.

PMID: 10441776
___________________________________________________________



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