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Use of gamma-tocopherol and its oxidative metabolite LLU-alpha in the treatment of disease

a technology of gamma-tocopherol and llu-alpha, which is applied in the field of use of gamma-tocopherol and its oxidative metabolite llu-alpha in the treatment of disease, can solve the problems of lack of causal connection, low investigation of the efficacy of supplementation with gamma-tocopherol, and reduced risk of disease, so as to prevent high blood pressure and reduce immune system response

Inactive Publication Date: 2001-10-18
LOMA LINDA UNIV MEDICAL CENT
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In consequence, vitamin E supplements are almost exclusively made of .alpha.-tocopherol and little investigation into the efficacy of supplementation with .gamma.-tocopherol has been conducted.
Several studies have proposed that vitamin E supplementation may prevent a plethora of ills but many of these studies fail to provide causal connections between vitamer supplementation and therapeutic benefit; they merely indicate that a high dietary or plasma concentration and supplemental intake of vitamin E is associated with a reduced risk of disease.
In fact, some studies have failed to demonstrate that tocopherol supplementation provides any protection from disease.

Method used

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  • Use of gamma-tocopherol and its oxidative metabolite LLU-alpha in the treatment of disease
  • Use of gamma-tocopherol and its oxidative metabolite LLU-alpha in the treatment of disease
  • Use of gamma-tocopherol and its oxidative metabolite LLU-alpha in the treatment of disease

Examples

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example 1

[0160] Human uremic urine was initially processed by ultrafiltration (3 kDa) and lyophilization, followed by isolation of the post-salt fraction from Sephadex G-25 gel filtration chromatography, following the procedure of Benaksas et al., Life Sci. 52, 1045-1054 (1993), the entire disclosure of which is herein incorporated by reference. See Table I (first purification step).

[0161] The crude material was further purified by one of two procedures. One procedure involved four sequential HPLC steps, and the second procedure included organic solvent extraction followed by up to five sequential HPLC steps. Table I summarizes the two methods.

1TABLE 1 Summary of steps used in the chromatographic and extraction isolation procedures Puri-fication Chromatographic Extraction Step Method Method First 3K ultrafiltration, 3K ultrafiltration, lyophilization lyophilization and G-25 and G-25 Second 0.2 M pyridinium acetate pH Sequential extraction with 5.5 / Methanol C.sub.18 RP-HPLC isopropanol / diethy...

example 2

[0178] 1. In Vivo Bioassay

[0179] The assay for natriuresis in conscious rats has been described previously (see Benaksas et al., above). The assay is briefly reiterated here. Female Sprague-Dawley (Harlan) rats (200-250 g) were cannulated in the femoral artery and vein for monitoring of mean arterial pressure (MAP) and Infusion of saline and samples, respectively. The bladder was catheterized for collection of urine in ten-minute periods. Furosemide (0.4 mg / kg bwt; 1 mg / mL in 0.17% saline) was infused as a positive control at the beginning of the sixth ten-minute period. The sample was infused at the beginning of the seventeenth ten-minute period. Urine was collected for another 150 minutes. The volume of the urine was determined gravimetrically and the Na.sup.+ and K.sup.+ concentrations determined with a Beckman E2A electrolyte analyzer. From these data the sodium excretion values (UNaV) were calculated.

[0180] The natriuretic response of a sample was normalized to the dose of furo...

example 3

[0187] In addition, spectroscopy other than UV was performed. .sup.13C-and .sup.1H-NMR spectra were recorded at 500.1357 MHz in deutero-Chloroform (99.9%) in a GN-500 spectrometer (General Electric). High resolution Electron-Impact (ED mass spectra with a resolution of 2000 were recorded at an ionization voltage of 70 eV, source temperature of 220.degree. C. and introduction of sample by direct probe on a VG7070 EHF high resolution mass spectrometer. Fourier-transform infrared (FT-IR) spectroscopy was performed on a Nicolet 5DX with 4 wavenumber resolution.

[0188] The IR and .sup.13C-NMR spectra of LLU-.alpha. provided evidence for the presence of a carboxylic acid group. This explained the tailing of LLU-.alpha. observed upon elution from isopropanol / hexane silica gel HPLC (sixth purification step). The presence of a carboxyl group was verified when the reaction of LLU-.alpha. with diazomethane resulted in a product that was less polar on RP-HPLC and had an exact mass 14 units great...

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Abstract

The present invention is generally related to the discovery of the therapeutic benefit of administering gamma-tocopherol and gamma-tocopherol derivatives. More specifically, the use of gamma-tocopherol and racemic LLU-alpha, (S)-LLU-alpha, or gamma-tocopherol derivatives as antioxidants and nitrogen oxide scavengers which treat and prevent high blood pressure, thromboembolic disease, cardiovascular disease, cancer, natriuretic disease, the formation of neuropathological lesions, and a reduced immune system response are disclosed.

Description

I. CROSS-REFERENCE TO RELATED APPLICATIONS[0001] This application claims priority to U.S. patent application Ser. No. 09 / 461,645, filed Dec. 14, 1999, which is a continuation application of U.S. patent application Ser. No. 09 / 215,608, filed Dec. 17, 1998, which are hereby expressly incorporated by reference in their entireties.II. FIELD OF INVENTION[0002] The present invention is generally related to the discovery of the therapeutic benefit of administering .gamma.-tocopherol and .gamma.-tocopherol derivatives. More specifically, the use of .gamma.-tocopherol and racemic LLU-.alpha., (S)-LLU-.alpha., or other .gamma.-tocopherol derivatives as antioxidants and nitrogen oxide scavengers which treat and prevent high blood pressure, thromboembolic disease, cardiovascular disease, cancer, natriuretic disease, the formation of neuropathological lesions, and a reduced immune system response are disclosed.III. BACKGROUND OF THE INVENTION[0003] Vitamin E, an essential fat-soluble vitamin, en...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/355C07D311/72A61K45/06A61P1/16A61P3/06A61P7/02A61P9/04A61P9/08A61P9/10A61P9/12A61P13/12A61P21/00A61P25/00A61P27/02A61P35/00A61P43/00
CPCA61K31/355A61K45/06A61K31/35A61K2300/00A61P1/16A61P13/12A61P21/00A61P25/00A61P27/02A61P35/00A61P3/06A61P37/04A61P43/00A61P7/02A61P9/00A61P9/04A61P9/08A61P9/10A61P9/12
Inventor WECHTER, WILLIAM J.
Owner LOMA LINDA UNIV MEDICAL CENT
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