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Back Lingoji™ (Lingzhi/Goji) |
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Goji Berries
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Goji Berries are a very rich source of vitamin C, having 500 times more
vitamin C per ounce than oranges, actually more almost any fruit you could
name. They are also a superb source of vitamin A, not surprising
because they are a really pretty red color. Goji berries also have
vitamins
B1, B2, B6, and E; they are becoming a famous antioxidant.
They are also a rich source of both selenium and germanium and have hence
been used in a number of clinical trials involving cancer patients. When
given to patients undergoing chemotherapy, the berries conferred significant
protection for the liver. In Oriental medicine, they are said to correct chi
deficiency, meaning that people with low energy, insomnia, heart
palpitations, and even anxiety are more comfortable after consuming Goji
berries. The berries have 18 amino acids (higher than bee pollen) and 21
trace minerals, linoleic acid, and more beta-carotene than carrots. They are
also a rich source of both selenium and germanium and have hence been used
in a number of clinical trials involving cancer patients. When given to
patients undergoing chemotherapy, the berries conferred significant
protection for the liver. In Oriental medicine, they are said to correct chi
deficiency, meaning that people with low energy, insomnia, heart
palpitations, and even anxiety are more comfortable after consuming Goji
berries. The berries have 18 amino acids (higher than bee pollen) and 21
trace minerals, linoleic acid, and more beta-carotene than carrots.
In vitro studies suggest that Goji berries kill many kinds of cancer cells.
The mechanism whereby this happens is believed to involve some factor that
inhibits the ability of the cell to divide, thus lowering its reproductive
capacity. A large study in Japan suggested that tumor growth was inhibited
by 58% among the patients eating Goji berries as compared to the control
groups. A study in Mongolia showed that patients eating the Goji berries had
a significant increase in lymphocyte activity and that their blood began to
resemble that of much younger persons. |
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Resources
Eur J Pharmacol. 2003 Jun 27;471(3):217-22.
[A polysaccharide-protein complex from Lycium barbarum upregulates
cytokine expression in human peripheral blood mononuclear cells.]
Gan L, Zhang SH, Liu Q, Xu HB.
Institute of Pharmacy, Huazhong University of Science and Technology, Wuhan
430074, People's Republic of China.
The production of cytokine is a key event in the initiation and regulation
of an immune response. Many compounds are now used routinely to modulate
cytokine production, and therefore the immune response, in a wide range of
diseases, such as cancer. Interleukin-2 and tumor necrosis factor-alpha are
two important cytokines in antitumor immunity. In this study, the effects of
Lycium barbarum polysaccharide-protein complex (LBP(3p)) on the expression
of interleukin-2 and tumor necrosis factor-alpha in human peripheral blood
mononuclear cells were investigated by reverse transcription polymerase
chain reaction (RT-PCR) and bioassay. Administration of LBP(3p) increased
the expression of interleukin-2 and tumor necrosis factor-alpha at both mRNA
and protein levels in a dose-dependent manner. The results suggest that
LBP(3p) may induce immune responses and possess potential therapeutic
efficacy in cancer.
PMID: 12826241 [PubMed - indexed for MEDLINE]
Wei Sheng Yan Jiu. 2000 Mar 30;29(2):115-117.
[ Isolation and purification of Lycium barbarum polysaccharides and its
antifatigue effect ]
[ Article in Chinese ]
Luo Q, Yan J, Zhang S.
Department of Hygiene, Hubei Medical University, Wuhan 430071, China.
A purified componenof lyceum barbarum polysaccharide (LBP-X) was isolated
from lyceum barbarum L. by DEAE ion-exchange cellulose and sephacryl gel
chromatography. LBP-X was tested on five different doses (5, 10, 20, 50 and
100 mg.kg-1.d-1) in mice. The results showed that LBP-X induced a remarkable
adaptability to exercise load, enhanced resistance and accelerated
elimination fatigue. LBP-X could enhance the storage of muscle and liver
glycogen, increase the activity of LDH before and after swimming, decrease
the increase of blood urea nitrogen (BUN) after strenuous exercise, and
accelerate the clearance of BUN after exercise. The dosage of LBP-X 10
mg.kg-1.d-1 was the best amount among the five tested doses.
PMID: 12725093 [PubMed- indexed for MEDLINE]
Wei Sheng Yan Jiu. 2002 Apr;31(2):118-119.
[Study on the composition of Lycium barbarum polysaccharides and its effects
on the growth of weanling mice]
[Article in Chinese]
Zhang M, Wang J, Zhang S.
Food Science Department, Huazhong Agricultural University, Wuhan 430070,
China.
In order to observe the effects of lycium barbarum polysaccharides (LBP-4)
on the growth of weanling mice and the absorption of some metals in the
their body, the composition of LBP-4 is determined. 120 female weanling mice
are divided in random into 4 groups. They are fed on LBP-4 at the dose of 5,
10 and 20 mg/(kg.d) respectively. The taken feed weight and the body weight
of mice are recorded everyday. After 21 days, the content of calcium,
magnesium, zinc and iron in pygal muscles and femora of mice is determined.
The results showed that LBP-4 is composed of six kinds of monosaccharides
that can enhance food conversion rate and the content of zinc and iron in
body of mice, and reduce the body weight.
PMID: 12561548 [PubMed - indexed for MEDLINE]
Zhongguo Zhong Yao Za Zhi. 1993 Feb;18(2):110-112, 128.
[Experimental research on the role of Lycium barbarum polysaccharide in
anti-peroxidation]
[Article in Chinese]
Zhang X.
Beijing Military General Hospital.
In this work, the changes in electrical parameters of cell membrane of
Xenopus Oocytes were determined using routine microelectrode
electrophysiological technique after incubation of the cells in frog Ringer
solution containing free radical producing system for 6 hours. It was
observed that the resting membrane potential was raised, and the membrane
resistance and time constant were decreased. The effects of free radical on
the cells can be prevented and reversed by incubation with superoxide
dismutase or Lycium barbarum polysaccharide.
PMID: 8323695 [PubMed - indexed for MEDLINE]
Breithaupt DE, Weller P, Wolters M, Hahn A. Comparison of plasma responses
in human subjects after the ingestion of 3R,3R'-zeaxanthin dipalmitate from
wolfberry (Lycium barbarum) and non-esterified 3R,3R'-zeaxanthin using
chiral high-performance liquid chromatography. Br J Nutr. 2004;91:707-13.
Cao GW, Yang WG, Du P. [Observation of the effects of LAK/IL-2 therapy
combining with Lycium barbarum polysaccharides in the treatment of 75 cancer
patients] Zhonghua Zhong Liu Za Zhi. 1994;16:428-31.
Dafni A,.Yaniv Z. Solanaceae as medicinal plants in Israel. J Ethnopharmacol.
1994;44:11-8.
Gan L, Wang J, Zhang S. [Inhibition the growth of human leukemia cells by
Lycium barbarum polysaccharide]. Wei Sheng Yan Jiu. 2001;30:333-5.
Gan L, Zhang SH, Liu Q, Xu HB. A polysaccharide-protein complex from Lycium
barbarum upregulates cytokine expression in human peripheral blood
mononuclear cells. Eur J Pharmacol. 2003;471:217-22.
Hakim IA, Harris RB, Chow HH, Dean M, Brown S, Ali IU. Effect of a 4-month
tea intervention on oxidative DNA damage among heavy smokers: role of
glutathione S-transferase genotypes. Cancer Epidemiol Biomarkers Prev.
2004;13:242-9.
Huang Y, Tan A, Shen Y, Lu J. [Scavenging effect of total flavonoids of
lycium barbarum L on active oxygen radicals and inhibitory effects on heat
output from L1210 cells] Wei Sheng Yan Jiu. 1998;27:109-11, 115.
Kimura H, Yamaguchi Y. A phase III randomized study of interleukin-2
lymphokine-activated killer cell immunotherapy combined with chemotherapy or
radiotherapy after curative or noncurative resection of primary lung
carcinoma. Cancer. 1997;80:42-9.
Lam AY, Elmer GW, Mohutsky MA. Possible interaction between warfarin and
Lycium barbarum L. Ann Pharmacother. 2001;35:1199-201.
Liu XL, Sun JY, Li HY, Zhang L, Qian BC. [Extraction and isolation of active
component for inhibiting PC3 cell proliferation in vitro from the fruit of
Lycium barbarum L.] Zhongguo Zhong Yao Za Zhi. 2000;25:481-3.
Lu CX, Cheng BQ. [Radiosensitizing effects of Lycium barbarum polysaccharide
for Lewis lung cancer] Zhong Xi Yi Jie He Za Zhi. 1991;11:611-2, 582.
Rosenberg SA, Lotze MT, Yang JC, et al. Prospective randomized trial of
high-dose interleukin-2 alone or in conjunction with lymphokine-activated
killer cells for the treatment of patients with advanced cancer. J Natl
Cancer Inst. 1993 ;85:622-32. |
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Red Reishi Mushroom Clinical
Information / Resources
Tao J, Feng K.Y. Experimental and clinical studies on inhibitory effect of
ganoderma
lucidum on platelet aggregation. J Tongji Med Univ 1990; 10(4): 240-243.
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Wasser SP, Weis AL. Therapeutic effects of substances occurring in higher Basidiomycetes mushrooms:
a modern perspective. Crit Rev Immunol 1999;
19(1): 65-96.
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el-Mekkawy S, Meselhy MR, Nakamura N, et al. Anti-HIV-1 and anti-HIV-1
protease substances from Ganoderma lucidum. Phytochemistry 1998; 49(6):
1661-1657.
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Kim RS, Kim HW, Kim BK. Suppressive effects of Ganoderma lucidum on
proliferation of peripheral blood mononuclear cells. Mol Cells 1997; 7(1):
52-57.
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Wang SY, Hsu ML, Hsu HC, et al. The anti-tumor effect of Ganoderma lucidum
is mediated by cytokines released from activated macrophages and T
lymphocytes. Int J Cancer 1997; 70(6): 699-705.
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Hijikata Y, Yamada S. Effect of Ganoderma lucidum on postherpetic meuralgia.
Am J Chin Med 1998;
26(3-4): 375-381.
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Kim HS, Kacew S, Lee BM. In vitro chemopreventive effects of plant
polysaccharides (Aloe barbadensis miller, Lentinus edodes, Ganoderma lucidum
and Coriolus versicolor). Carcinogenesis 1999; 20(8):
1637-1640.
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Komoda Y, Shimizu M, Sonoda Y, et al. Ganoderic acid and its derivatives as
cholesterol synthesis inhibitors; Chem Pharm Bull (Tokyo) 1989; 37(2):
531-533. |
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Hikino H, Ishiyama M, Suzuki Y, et al. Mechanisms of hypoglycemic activity
of ganoderan B: a glycan of Ganoderma lucidum fruit bodies. Planta Med 1989;
55(5): 423-428.
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Lee SY, Rhee HM. Cardiovascular effects of mycelium extract of Ganoderma
lucidum: inhibition of sympathetic outflow as a mechanism of its hypotensive
action. Chem Pharm Bull (Tokyo) 1990; 38(5):
1359-1364.
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Kim DH, Shim SB, Kim NJ, et al. Beta-glucuronidase-inhibitory activity and
hepatoprotective effect of Ganoderma lucidum. Biol Pharm Bull 1999; 22(2):
162-164.
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Yoon SY, Eo SK, Kim YS, et al. Antimicrobial activity of Ganoderma lucidum
extract alone and in combination with some antibiotics. Arch Pharm Res 1994;
17(6): 438-442.
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Chen K, Li C. Recent advances in studies on traditional Chinese anti-aging
material medica. J Tradit Chin Med 1993; 13(3): 223-226.
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van der Hem LG, van der Vliet JA, Bocken CF, et al. Ling Zhi-8; studies of a
new immunomodulating agent. Transplanation 1995; 60(5): 438-443.
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Thomas Bartram Fellow of the National Institute of Medical Herbalists,
Bartram's Encyclopedia of Herbal Medicine, the Definite Guide to the Herbal
Treatment of Diseases: 368.
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Linda B. White M.D., Steven Foster. The Herbal Drugstore: 570.
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John E. Smith, Neil J. Rowan, Richard Sullivan. Medicinal Mushrooms and
Cancer; (2):15; (3):26; (3):27-32; (7); (8).
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Terry Willard, PhD. Reishi Mushroom Herb of Spiritual Potency and Medical
Wonder; (3); (4); (5).
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Huang K. The Pharmacology of Chinese Herbs, 2nd ed. New York: CRC Press;
1999.
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Hobbs C. Medicinal Mushrooms, 3rd ed. Loveland (CO): Interweave Press; 1996.
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Mao T, et al. Two mushrooms, Grifola frondosa and Ganoderma lucidum, can
stimulate cytokine gene expression and proliferation in human T lymphocytes.
Int J Immunother 1999;15: 13-22.
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Shiao MS, et al. Natural products and biological activities of Ganoderma
lucidum. Am Chem Soc 1994;
342-354.
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Mizuno T, et al. Reishi, Ganoderma lucidum and Ganoderma tsugae: Bioactive
substances and medicinal effects. FD Rev Inter 1995;11: 151-166.
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Furusawa E, et al. Antitumor activity of Ganoderma lucidum, on
intraperitoneally implant Lewis lung carcinoma in synergistic mice.
Phytother Res 1992;6: 300-304.
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Hsu MJ, Lee SS, Lin WW. Polysaccharide purified for Ganoderma lucidum
inhibits spontaneous and Fas-mediated apoptosis in human neutrophils through
activation of the phosphatidylinositol 3 kinase/Akt signaling pathway. J
Leukoc Biol 2002;72: 207-216.
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Gao Yihuai, et al. Mechanism of the antiulcerogenic effect of Ganoderma
lucidum polysaccharides on indomethacin-induced lesions in the rat. Life Sci.
2002 Dec 27;72(6): 731-745. |
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Chen HS, et al. Studies on the immuno-modulating and anti-tumor activities
of Ganoderma lucidum (Reishi) polysaccharides. Bioorg Med Chem. 2004 Nov
1;12 (21): 5595-5601.
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Gao Y, et al. Effects of ganopoly (a Ganoderma lucidum polysaccharide
extract) on the immune functions in advanced-stage cancer patients. Immunol
Invest. 2003 Aug;32(3): 201-215.
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Wachtel-Galor S, et al. Ganoderma lucidum (‘Lingzhi'); acute and short-term
biomarker response to supplementation. Int J Food Sci Nutr. 2004 Feb;55(1):
75-83. |
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Wachtel-Galor S, Tomlinson B, Benzie IF. Ganoderma lucidum ("Lingzhi"), a
Chinese medicinal mushroom: biomarker responses in a controlled human
supplementation study. Br J Nutr. 2004 Feb;91(2): 263-269.
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Futrakul N, et al. Ganoderma lucidum suppresses endothelial cell
cytotoxicity and proteinuria in persistent proteinuric focal segmental
glomerulosclerosis (FSGS) nephrosis. Clin Hemorheol Microcirc. 2004;31(4):
267-272.
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