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2. Conplastic strains for identification of retrograde effects of mitochondrial dna variation on cardiometabolic traits in the spontaneously hypertensive rat

Creator:
Pravenec, Michal, Šilhavý, Jan, Mlejnek, Petr, Šimáková, Miroslava, Mráček, Tomáš, Pecinová, Alena, Tauchmannová, Kateřina, Hütl, Martina, Malínská, Hana, Kazdová, Ludmila, Neckář, Jan, Kolář, František, Žurmanová, Jitka, Novotný, Jiří, and Houštěk, Josef
Format:
počítač and online zdroj
Type:
model:article and TEXT
Subject:
mitochondrial DNA, conplastic strains, spontaneously hypertensive rat, glucose and lipid metabolism, and cardiac traits
Language:
English
Description:
Mitochondrial retrograde signaling is a pathway of communication from mitochondria to the nucleus. Recently, natural mitochondrial genome (mtDNA) polymorphisms (haplogroups) received increasing attention in the pathophysiology of human common diseases. However, retrograde effects of mtDNA variants on such traits are difficult to study in humans. The conplastic strains represent key animal models to elucidate regulatory roles of mtDNA haplogroups on defined nuclear genome background. To analyze the relationship between mtDNA variants and cardiometabolic traits, we derived a set of rat conplastic strains (SHR-mtBN, SHR-mtF344 and SHR-mtLEW), harboring all major mtDNA haplotypes present in common inbred strains on the nuclear background of the spontaneously hypertensive rat (SHR). The BN, F344 and LEW mtDNA differ from the SHR in multiple amino acid substitutions in protein coding genes and also in variants of tRNA and rRNA genes. Different mtDNA haplotypes were found to predispose to various sets of cardiometabolic phenotypes which provided evidence for significant retrograde effects of mtDNA in the SHR. In the future, these animals could be used to decipher individual biochemical components involved in the retrograde signaling.
Rights:
http://creativecommons.org/licenses/by-nc-sa/4.0/ and policy:public

3. High cysteine diet reduces insulin resistance in SHR-CRP rats

Creator:
Krijt, Jakub, Sokolová, Jitka, Šilhavý, Jan, Mlejnek, Petr, Kubovčiak, Jan, Liška, František, Malínská, Hana, Hüttl, Martina, Marková, Irena, Křížková, Michaela, Stipanuk, Martha H., Křížek, Tomáš, Ditroi, Tamas, Nagy, Peter, Kožich, Viktor, and Pravenec, Michal
Format:
počítač and online zdroj
Type:
model:article and TEXT
Subject:
inzulinová rezistence, insulin resistance, SHR-CRP rats, metabolic syndrome, taurine, cysteine, cysteine dioxygenase, 14, and 612
Language:
English
Description:
Increased plasma total cysteine (tCys) has been associated with obesity and metabolic syndrome in human and some animal studies but the underlying mechanisms remain unclear. In this study, we aimed at evaluating the effects of high cysteine diet administered to SHR-CRP transgenic rats, a model of metabolic syndrome and inflammation. SHR-CRP rats were fed either standard (3.2 g cystine/kg diet) or high cysteine diet (HCD, enriched with additional 4 g L-cysteine/kg diet). After 4 weeks, urine, plasma and tissue samples were collected and parameters of metabolic syndrome, sulfur metabolites and hepatic gene expression were evaluated. Rats on HCD exhibited similar body weights and weights of fat depots, reduced levels of serum insulin, and reduced oxidative stress in the liver. The HCD did not change concentrations of tCys in tissues and body fluids while taurine in tissues and body fluids, and urinary sulfate were significantly increased. In contrast, betaine levels were significantly reduced possibly compensating for taurine elevation. In summary, increased Cys intake did not induce obesity while it ameliorated insulin resistance in the SHR-CRP rats, possibly due to beneficial effects of accumulating taurine., Jakub Krijt, Jitka Sokolová, Jan Šilhavý, Petr Mlejnek, Jan Kubovčiak, František Liška, Hana Malínská, Martina Hüttl, Irena Marková, Michaela Křížková, Martha H. Stipanuk, Tomáš Křížek, Tamas Ditroi, Peter Nagy, Viktor Kožich, Michal Pravenec., and Obsahuje bibliografii
Rights:
http://creativecommons.org/licenses/by-nc-sa/4.0/ and policy:public