Effects of α-Melanocortin Enantiomers on Acetaminophen-Induced Hepatotoxicity in CBA Mice

被引:10
作者
Turcic, Petra [2 ]
Bradamante, Mirna [3 ]
Houra, Karlo [4 ]
Stambuk, Nikola [1 ]
Kelava, Tomislav [5 ]
Konjevoda, Pasko [1 ]
Kazazic, Sasa [1 ]
Vikic-Topic, Drazen [1 ]
Pokric, Biserka [1 ]
机构
[1] Rudjer Boskovic Inst, Zagreb 10002, Croatia
[2] Univ Zagreb, Dept Pharmacol, Fac Pharm & Biochem, Zagreb 10000, Croatia
[3] Univ Hosp, Ctr Zagreb, Dept Dermatol & Venerol, Zagreb 10000, Croatia
[4] Univ Hosp Sestre Milosrdnice, Dept Neurosurg, Zagreb 10000, Croatia
[5] Univ Zagreb, Sch Med, Dept Physiol & Immunol, Zagreb 10000, Croatia
来源
MOLECULES | 2009年 / 14卷 / 12期
关键词
enantiomer; alpha-MSH; hepatoprotection; hepatotoxicity; antibody; CD spectroscopy; D-AMINO ACIDS; MELANOCYTE-STIMULATING HORMONE; IN-VITRO; PEPTIDES;
D O I
10.3390/molecules14125017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins and peptides in mammals are based exclusively on L-amino acids. Recent investigations show that D-amino acids exhibit physiological effects in vivo, despite of their very small quantities. We have investigated the hepatoprotective effects of the Land D-enantiomers of alpha-melanocortin peptide (alpha-MSH). The results showed that peptide-enantiomerism is related to the protective effects of melanocortin peptides in vivo. L-alpha-MSH exhibited potent hepatoprotective effect in the experimental model of acetaminophen induced hepatotoxicity in male CBA mice, while its D-mirror image was inefficient. Furthermore, the antibody to the L-peptide did not recognize the D-structure. The results indicate that the opposite peptide configuration may be used to modulate its function and metabolism in vivo and in vitro.
引用
收藏
页码:5017 / 5026
页数:10
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