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1.
Ukr Biokhim Zh (1999) ; 79(5): 196-203, 2007.
Article in Russian | MEDLINE | ID: mdl-18357794

ABSTRACT

It has been shown that a three-week feeding of rats with oil derived from seeds of amaranth (Amaranthus cruentus L.) leads to a moderate activation of respiration of coupled and uncoupled rat liver mitochondria (MCh) that oxidize succinate and succinate + glutamate, as well as alpha-ketoglutarate and alpha-ketoglutarate + malonate. In animals receiving the amaranth oil, the injection of adrenaline did not affect the oil-activated respiration of MCh during succinate oxidation; i. e., animals prepared by an oil-enriched diet were resistant to the action of adrenaline, which prevented from possible hyperactivation of mitochondrial functions. In the group of control animals, which received no oil, the injection of adrenaline activated the rate of phosphorylating respiration of MCh during oxidation of succinate or succinate + glutamate: the rate of oxygen uptake in state 3 respiration (by Chance) increased, and the phosphorylation time decreased. The injection of adrenaline did not affect the parameters of respiration of MCh that oxidize a-ketoglutarate; however, in the presence of malonate, the oxidation of alpha-ketoglutarate in state 3 and uncoupled respiration have shown mild but significant increase in response to adrenaline. In animals receiving the amaranth oil, the oil-induced activation of respiration of MCh in response to adrenaline retained but did not increase; however, the phosphorylation time significantly decreased. Thus, concentrated oil of seeds activates the respiration of MCh. In addition, it enhances an energetic function of MCh, which prevents from the hyper-activation of mitochondrial respiration by adrenaline. Therefore an activation of energetic function of MCh by amaranth oil could explain its adaptogenic effect on rats.


Subject(s)
Amaranthus/chemistry , Energy Metabolism/drug effects , Epinephrine/pharmacology , Liver/drug effects , Mitochondria, Liver/drug effects , Plant Oils/pharmacology , Animals , Dose-Response Relationship, Drug , Liver/metabolism , Male , Mitochondria, Liver/metabolism , Oxidative Stress/drug effects , Plant Oils/isolation & purification , Rats , Rats, Wistar , Seeds/chemistry
2.
Mol Gen Mikrobiol Virusol ; (3): 29-33, 2003.
Article in Russian | MEDLINE | ID: mdl-12966924

ABSTRACT

Tetanus belongs to dangerous infection diseases, whose effective prevention can be ensured by vaccines. The acting substance of tetanus vaccines, presently in use, is a partially purified and deprived-of-lethal-action Clostridium tetani neurotoxin. The construction of a subunit preparation on the basis of toxin fragments obtained through gene engineering could be a method aimed at promoting the quality of the used tetanus vaccines. With this goal in mind, we built, within the present case study, the expressing genetic constructions and obtained, in the pure form, an extensive tetanus-vaccine chain with its C-terminal (Hc) fragment, hydride peptides, containing the Hc-fragment and C-terminal fragment of toxin B C. difficile, as well as Hc-fragment and S3 collagen-binding domain of collagenase C. histolyticum. The thus obtained proteins can be used in testing their immunogenic and protective properties, while the conducted study could be a basis for further research of a new-generation vaccine against tetanus and other human infection diseases.


Subject(s)
Peptide Fragments/genetics , Recombinant Proteins/genetics , Tetanus Toxin/genetics , Vaccines, Synthetic/genetics , Binding Sites , Cloning, Molecular , Clostridioides difficile/genetics , Clostridium/genetics , Collagenases/genetics , Drug Design , Peptide Fragments/immunology , Plasmids , Protein Engineering/methods , Recombinant Proteins/immunology , Recombinant Proteins/metabolism , Tetanus/prevention & control , Tetanus Toxin/immunology , Tetanus Toxin/metabolism , Vaccines, Synthetic/immunology
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