| Name | muscles |
|---|---|
| Synonyms | COX 7a M; COX VIIa M; COX7A; COX7A1; COX7A1 protein; COX7AH; COX7AM; Cytochrome c oxidase subunit 7a H… |
| Name | cyanamide |
|---|---|
| CAS | cyanamide |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 12198016 | Niemela O, Parkkila S, Koll M, Preedy VR: Generation of protein adducts with malondialdehyde and in muscles with predominantly type I or type II fibers in rats exposed to and the dehydrogenase inhibitor cyanamide. Am J Clin Nutr. 2002 Sep;76(3):668-74. |
32(0,1,1,2) | Details |
| 16131499 | Patel VB, Worrall S, Emery PW, Preedy VR: Protein adduct species in muscle and liver of rats following acute administration. Alcohol Alcohol. 2005 Nov-Dec;40(6):485-93. Epub 2005 Aug 30. These were used to assay different adduct species in soleus (type I fibre-predominant) and plantaris (type II fibre-predominant) muscles and liver in four groups of rats administered acutely with either [A] saline (control); [B] cyanamide (an aldehyde dehydrogenase inhibitor); [C] [D] cyanamide+ethanol. |
32(0,1,1,2) | Details |
| 1449559 | Preedy VR, Keating JW, Peters TJ: The acute effects of and on rates of protein synthesis in type I and type II fibre-rich skeletal muscles of the rat. Alcohol Alcohol. 1992 May;27(3):241-51. Young rats were injected with either (75 mmol/kg), (2.8 mmol/kg) or isovolumetric amounts of NaCl (0.15 mol/l, i.e. controls) with or without inhibitors of alcohol dehydrogenase (4-methylpyrazole) or aldehyde dehydrogenase (cyanamide). After 2.5 hr, fractional rates of protein synthesis (i.e. ks) in the soleus (Type I fibre-rich) and plantaris (Type II fibre-rich) muscles were measured. |
2(0,0,0,2) | Details |
| 16784954 | Nakahara T, Hunter R, Hirano M, Uchimura H, McArdle A, Broome CS, Koll M, Martin CR, Preedy VR: alters skeletal muscle heat shock protein gene expression in rats: these effects are moderated by sex, raised endogenous and starvation. Metabolism. 2006 Jul;55(7):843-51. To address this, (i) male and female rats were fed in the long-term (6-7 weeks as 35% of energy in a liquid diet) and compared to controls fed the same diet with isoenergetic (ii) male rats given an immediate bolus (75 mmol per kilogram body weight intraperitoneally) 2.5 hours before sacrifice and compared to controls given a dose of saline (with or without pretreatment with cyanamide-an dehydrogenase inhibitor which raises endogenous (iii) male rats starved for 1 or 2 days then immediately dosed with Protein levels of HSP 27, HSP 60, and HSP 70 were measured in muscles of male rats fed and pair-fed control rats by SDS-PAGE and Western blotting in study I. |
1(0,0,0,1) | Details |
| 11782879 | Koll M, Ahmed S, Mantle D, Donohue TM, Palmer TN, Simanowski UA, Seltz HK, Peters TJ, Preedy VR: Effect of acute and chronic treatment and their superimposition on lysosomal, cytoplasmic, and proteosomal protease activities in rat skeletal muscle in vivo. Metabolism. 2002 Jan;51(1):97-104. We hypothesized that altered protease activities contribute to this phenomenon, and that differential effects on protease activities may occur when: (1) rats at different stages in their development are administered in vivo; (2) acute treatment is superimposed on chronic -feeding in vivo; and (3) muscles are exposed to and in vivo and in vitro. Other studies included administration of cyanamide (aldehyde dehydrogenase inhibitor) in vivo or addition of and to muscle preparations in vitro. |
1(0,0,0,1) | Details |
| 11337982 | Adachi J, Asano M, Ueno Y, Marway JS, Camilleri PM, Peters TJ, Preedy VR: Acute effect of on 7-hydroperoxycholesterol in muscle and liver. . Lipids. 2001 Mar;36(3):267-71. We tested the hypotheses that sensitivities of muscle and liver can be discerned in the initial periods of exposure, especially when levels are markedly raised with cyanamide, an aldehyde dehydrogenase inhibitor. This is the first report of a differential response of 7 alpha-OOH and 7 beta-OOH in Type II, compared to Type I predominant muscles, and the first time that muscle has been shown to be more sensitive than the liver in terms of its lipid marker response to oxidative stress. |
1(0,0,0,1) | Details |