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1.
Article in English | IMSEAR | ID: sea-23064

ABSTRACT

BACKGROUND & OBJECTIVE: Nicotine intake through tobacco is very common in female population of lower socioeconomic level who are deprived of healthy diet. Women suffer consequences of smoking such as cardiovascular disorder, lung related diseases and oxidative stress, etc. No data are available of the influences of nicotine on lipid profile, lipid peroxidation and antioxidant enzymes levels under restricted dietary protein intake. The present study was carried out to investigate the effect of nicotine on such parameters of female rats fed with protein restricted diet (5% casein) as compared to those with normal protein diet (18% casein) with or without vitamin C or E supplementation. METHODS: Subcutaneous injections of nicotine tartrate (3.5 mg/kg body weights per day for 15 days) were given to the rats and subsequent measurements of plasma lipid profile, plasma and ovary lipid peroxidation and antioxidant enzymes were done. RESULTS: The results showed significant (P<0.01) increase of total cholesterol (TC) and more significant (P<0.001) increase of triglyceride and low-density lipoprotein cholesterol (LDL-C) of plasma under both dietary conditions. The increase of plasma very low-density lipoprotein cholesterol (VLDL-C) was highly significant under protein-restricted diet. The high-density lipoprotein cholesterol (HDLC) decreased significantly in both dietary conditions. Lipid peroxidation in plasma increased significantly in protein-restricted condition. Superoxide dismutase and catalase activities in the ovary tissue decreased significantly (P<0.001) by nicotine treatment in both dietary groups. INTERPRETATION & CONCLUSION: Our findings indicated that nicotine-induced toxicity is more in lipid profile (plasma) and lipid peroxidation (plasma and ovary tissue) under protein-restricted diet as compared to that of the normal protein diet. The antioxidant vitamins antagonized the nicotineinduced effects less effectively on the observed parameters under restricted dietary protein.


Subject(s)
Animals , Antioxidants/metabolism , Catalase/metabolism , Diet, Protein-Restricted/adverse effects , Female , Humans , Lipid Peroxidation/drug effects , Lipids/blood , Nicotine/toxicity , Ovary/drug effects , Rats , Rats, Wistar , Superoxide Dismutase/metabolism
2.
Indian J Exp Biol ; 2006 Apr; 44(4): 336-9
Article in English | IMSEAR | ID: sea-59191

ABSTRACT

In the biosphere, bacteria can function as geo-chemical agents, promoting the dispersion, fractionation and/or concentration of materials. Microbial mineral precipitation is resulted from metabolic activities of microorganisms. Based on this biomineralogy concept, an attempt has been made to develop bioconcrete material incorporating of an enrichment culture of thermophilic and anaerobic bacteria within cement-sand mortar/concrete. The results showed a significant increase in compressive strength of both cement-sand mortar and concrete due to the development of filler material within the pores of cement sand matrix. Maximum strength was observed at concentration 10(5)cell/ml of water used in mortar/concrete. Addition of Escherichia coil or media composition on mortar showed no such improvement in strength.


Subject(s)
Anaerobiosis , Biomass , Cells, Cultured , Compressive Strength , Construction Materials , Shewanella/growth & development , Silicon Dioxide , Temperature , Time Factors
3.
Indian J Exp Biol ; 2004 Mar; 42(3): 330-2
Article in English | IMSEAR | ID: sea-63098

ABSTRACT

Nicotine causes decrement in body weight, reduction in ovarian and uterine weight, irregularity in estrous cycle and histological damage in ovary and uterus in rats maintained on normal (18% casein) and protein restricted diet (5% casein). The degree of nicotine toxicity increases in protein inadequacy.


Subject(s)
Animals , Body Weight/drug effects , Caseins/metabolism , Diet, Protein-Restricted , Female , Nicotine/pharmacology , Organ Size/drug effects , Ovary/metabolism , Rats , Rats, Wistar , Uterus/metabolism
4.
Indian J Exp Biol ; 2003 Aug; 41(8): 915-7
Article in English | IMSEAR | ID: sea-58789

ABSTRACT

Methane emission was inhibited by aluminium ion in paddy fields. Addition of Al3+ (20 mM) to the culture medium containing cells of pure Methanosarcina barkeri, inhibited methanogenesis. Methanogenic co-factor, F-420, was isolated and purified from Methanosarcina barkeri MS. Spectrophotometric and spectrofluorometric analysis of interaction between co-factor, F-420, and Al3+ revealed that they formed a complex compound that might have blocked methanogenesis.


Subject(s)
Aluminum Compounds/chemistry , Cations , Drug Interactions , Electron Transport , Methane/metabolism , Methanosarcina barkeri/drug effects , Oxidoreductases/chemistry , Spectrometry, Fluorescence
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