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Vitamin Alcoholism

The first example is the plasma-borne retinol-binding protein, RBP, which is a single polypeptide chain of 182 amino acid residues. This protein is responsible for transporting the lipid alcohol vitamin A (retinol) from its storage site in the liver to the various vitamin-A-dependent tissues. It is a disposable package in the sense that each RBP molecule transports only a single retinol molecule and is then degraded. [Pg.68]

When utilization tests were run on a group of 18 male and 7 female human subjects, wide variations in blood level responses were found, particularly among the males.36 [Both in animals (rats) and humans the two sexes respond somewhat differently.] When 134,000 ig. of vitamin A in four different forms, viz., vitamin A alcohol, vitamin A acetate, vitamin A natural ester No. 1, and vitamin A natural ester No. 2, was fed to the group of 18 males on four different occasions, the serum levels found after 6 hours ranged from 178 to 1423 ig. per 100 ml., 122 to 1170 ig. per 100 ml., 110 to 1183 ig. per 100 ml., and 114 to 1230 ig. per 100 ml., respectively. These nearly 10-fold variations in serum levels do not, of course, indicate 10-fold variation in need, but they do show that the vitamin when given in relatively large doses does behave very differently in different individuals. [Pg.190]

Many useful compounds such as amino acids, nucleic acids, alcohols, vitamins, antibiotics, foods, etc. are produced in fermentation industries. Furthermore, many organic and inorganic compounds are present in waste waters. The determination of these compounds is required for control of fermentation and environment. Analysis of these compounds can be done by spectrophotometric methods. However, complicated procedures and long reaction times are required. [Pg.330]

ALCOHOL VITAMIN C (large doses, e.g. 1000 mg) May t elimination of alcohol, but this is unproven Uncertain Unlikely to be of clinical significance... [Pg.719]

Leo MA, Lieber CS. Alcohol, vitamin A, and beta-carotene adverse interactions, including hepatotoxicity and carcinogenicity. Am J Clin Nutr 1999 69(6) 1071-85. [Pg.3653]

With 5 ttiM of the phenol, small PDls (< 1.2) were achieved from an early stage to a later stage of polymerization. Thus, the precursor method was confirmed to be useful. Other phenols were also effective (Figure 3 and Table 1 (entries 4-7)). They include a common antioxidant BHT, phenol itself, a natural compound vitamin E (VE), and also a vinyl alcohol vitamin C (VC). The use of BPB (instead of VRl 10) led to a faster polymerization as in the TT system (Table 1 (entries 8-12)). [Pg.165]

Chromatographic fractionation CO2 + alcohol Vitamins, polyunsaturated fatty acids... [Pg.1444]

Mono- and sesquiterpenes are the main constituents of the essential oils, while the other terpenes are constituents of balsams, resins, waxes, and rubber. Oleoresin is a roughly equal mixture of turpentine (85 % Cio-monoterpenes and 15 % C15- sesquiterpenes) and rosin (C2o-diterpene) that acts in many conifer species as a toxic material to invading insects and their pathogenic fungi [12]. A number of angiosperm species have inducible terpenoid defensive compounds (phytoalexins) [13]. These include both sesquiterpenoid and diterpenoid t)pes. Isoprenoid units are also found within the framework of other natural molecules. Thus, indole alkaloids, several quinones (vitamin K), alcohols (vitamin E, vitamin A formed from p-carotene), phenols, and isoprenoid alcohols (also known as terpenols or polyprenols) also contain terpenoid fragments. The biogenesis. [Pg.2670]

Non-nucleotide pol inhibitors have been discovered among different classes of namral and synthetic chemical compounds. The main of them are long-chain fatty acids, fatty acid derivatives, bile acid derivatives, steroid derivatives, triterpenoids, cerebrosides, alkaloids, flavonoids, anthocyanins, glycolipids, catechins, coenzyme Qs, isosteviols, dipeptide alcohols, vitamins, etc. [52, 53]. The most well-studied non-nucleotide inhibitors are presented in Table 4.2. [Pg.105]

Beta-adrenoceptor antagonists arthralgia, 11.164 sexual function, 15.188 Beta-carotene, see also Vitamin A alcohol, vitamin A, interaction, 24.442 tumorigenicity, 25.454 Beta-lactam antibiotics effects on eukaryotic cells, 13.212 immediate hypersensitivity reactions, 14.211 pregnancy, 25.280 Blood, see Transfusions Botulinum toxin A, use in primary axillary hyperhidrosis, 27.161... [Pg.1117]

Alcoholism. Alcoholics make up abrout 10% of the first admissions to psychiatric wards. They possess some of the same symptoms noted in thiamin deficiency, and indeed respond to thiamin therapy. Often Korsakoff s syndrome— confusion, confabulation, fear, impaired learning, delirium— is associated with alcoholism. Vitamin therapy helps to restore the individual s attentiveness, alertness, and responsiveness. [Pg.689]

C20H30O Retinol alcohol (Vitamin A) Retinol (Alkohol) 20.020/00.205 J6/1... [Pg.312]

We used such an approach in the study of dissociative edep reduction of the p, y-unsaturated alcohols. Specially synthesized deuterated 2,4-pentadienol and its derivatives CH2=CHCH=CHCD2Y, where Y = -OH, -OAc, and -OMe, was taken as a substrate RY [272,273] the deuterium label is necessary to distinguish the 1,5-positions. In contrast to the cases studied earlier (cinnamic alcohol, vitamin A, etc.. Sect. 9.2.2, Natural Polyenes Vitamins A and D, Carotenes, and Porphyrins ), the reaction proceeds here via the symmetric pentadienyl anion [CH2-CH-CH-CH-CD2]. Therefore, two piperylene isomers CH3-CH=CH-CH=CD2 (a) and CH2=CH-CH=CH2-CD2H (h) in the strictly equal amounts could be anticipated as products. However, the preferential formation of one isomer, with the rexp= [a]/ m > 2, was found experimentally. This anomaly was explained by nonequUibrium asymmetric arrangement of anion near the electrode due to the orientation inheritance of the original asynunetric molecule RY. This should lead to the intra-anion... [Pg.298]

Figure 6.23 The solubility of vitamins in solutions of sucrose esters of varying alkyl chain length as shown by transmittance data, illustrating maximum solubilization at C q and Ci2. O—O vitamin A alcohol — vitamin D2 — vitamin A acetate. Ratio of vitamin ester water 1 6 200. Drawn from the data of Mima [174]. Figure 6.23 The solubility of vitamins in solutions of sucrose esters of varying alkyl chain length as shown by transmittance data, illustrating maximum solubilization at C q and Ci2. O—O vitamin A alcohol — vitamin D2 — vitamin A acetate. Ratio of vitamin ester water 1 6 200. Drawn from the data of Mima [174].
Uses Solubilizer, emulsifier for cosmetics emulsifier for hydrophobic substances, e.g., fatty adds, fatty alcohols, vitamins, actives soiubiiizerfor essential oils and perfumes in water and water-alcohol mixts. [Pg.281]


See other pages where Vitamin Alcoholism is mentioned: [Pg.163]    [Pg.70]    [Pg.327]    [Pg.1194]    [Pg.217]    [Pg.668]    [Pg.442]    [Pg.361]    [Pg.70]    [Pg.81]    [Pg.82]    [Pg.1123]    [Pg.1125]    [Pg.1126]    [Pg.169]    [Pg.199]    [Pg.277]    [Pg.13]   
See also in sourсe #XX -- [ Pg.266 ]




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Alcohol dehydrogenase, vitamin

Alcohol vitamin A and

Alcohol vitamin deficiencies

Alcohol vitamin interactions

Alcoholics and vitamin

All-trans-vitamin A alcohol

Liver alcohol dehydrogenase vitamin

Vitamin A alcohol

Vitamin alcohol

Vitamin alcohol

Vitamin alcohol, beta-carotene, interaction

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