Hepatic Met-enkephalin immunoreactivity is enhanced in primary biliary cirrhosis

被引:52
作者
Bergasa, NV
Liau, S
Homel, P
Ghali, V
机构
[1] Beth Israel Deaconess Med Ctr, Div Gastrointestinal & Liver Dis, New York, NY 10003 USA
[2] Beth Israel Deaconess Med Ctr, Dept Pathol, New York, NY 10003 USA
[3] Beth Israel Deaconess Med Ctr, Off Grants Management & Res Suppport, New York, NY 10003 USA
来源
LIVER | 2002年 / 22卷 / 02期
关键词
endogenous opioids; primary biliary cirrhosis; liver; neuroendocrine;
D O I
10.1034/j.1600-0676.2002.01458.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/aims: In contrast to the normal adult liver, the fetal human and rat livers, and the liver of rats with cholestasis secondary to bile duct resection (BDR) express the preproenkephalin (ppENK) mRNA, which codes for the endogenous opioid peptide Met-enkephalin. In addition, Met-enkephalin immunoreactivity (MEIR) is detected in hepatocytes and in proliferating bile ductules in the cholestatic rat liver. These data suggest that cholestasis is associated with the resurgence of cells that produce Met-enkephalin. To explore further the status of opioids in cholestasis, we studied the expression of MEIR in liver tissue. Methods: The MEIR was sought in paraffin-preserved liver tissues from patients with primary biliary cirrhosis (PBC) (n = 10). Results: The MEIR was detected in all the PBC livers. Its intensity varied from weak to strong on hepatocytes and bile ducts and the strongest expression appeared as coarse granules. The MEIR was either absent or only faintly expressed by some hepatocytes from disease and nondisease control biopsies, but absent from bile ducts. Conclusion: These results suggest that the human liver in cholestasis may be a source of endogenous opioids.
引用
收藏
页码:107 / 113
页数:7
相关论文
共 44 条
[1]  
[Anonymous], OPIATES ENDOGENOUS O
[2]  
Bergasa NV, 1996, LIVER, V16, P298
[3]   THE PRURITUS OF CHOLESTASIS - POTENTIAL PATHOGENIC AND THERAPEUTIC IMPLICATIONS OF OPIOIDS [J].
BERGASA, NV ;
JONES, EA .
GASTROENTEROLOGY, 1995, 108 (05) :1582-1588
[4]   CHOLESTASIS IS ASSOCIATED WITH PREPROENKEPHALIN MESSENGER-RNA EXPRESSION IN THE ADULT-RAT LIVER [J].
BERGASA, NV ;
SABOL, SL ;
YOUNG, WS ;
KLEINER, DE ;
JONES, EA .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1995, 268 (02) :G346-G354
[5]   Oral nalmefene therapy reduces scratching activity due to the pruritus of cholestasis: A controlled study [J].
Bergasa, NV ;
Alling, DW ;
Talbot, TL ;
Wells, MC ;
Jones, EA .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1999, 41 (03) :431-434
[6]   LACK OF HEPATIC EXPRESSION OF PREPROENKEPHALIN (PPENK) MESSENGER-RNA IN PRIMARY BILIARY-CIRRHOSIS - ABSENCE OF A PREDOMINANT HISTOLOGICAL LESION [J].
BERGASA, NV ;
SABOL, SL ;
YOUNG, WS ;
KLEINER, D ;
JONES, EA .
HEPATOLOGY, 1993, 18 (04) :A210-A210
[7]   EFFECTS OF NALOXONE INFUSIONS IN PATIENTS WITH THE PRURITUS OF CHOLESTASIS - A DOUBLE-BLIND, RANDOMIZED, CONTROLLED TRIAL [J].
BERGASA, NV ;
ALLING, DW ;
TALBOT, TL ;
SWAIN, MG ;
YURDAYDIN, C ;
TURNER, ML ;
SCHMITT, JM ;
WALKER, EC ;
JONES, EA .
ANNALS OF INTERNAL MEDICINE, 1995, 123 (03) :161-167
[8]   Open-label trial of oral nalmefene therapy for the pruritus of cholestasis [J].
Bergasa, NV ;
Schmitt, JM ;
Talbot, TL ;
Alling, DW ;
Swain, MG ;
Turner, ML ;
Jenkins, JB ;
Jones, EA .
HEPATOLOGY, 1998, 27 (03) :679-684
[9]  
Bhargava H N, 1990, NIDA Res Monogr, V96, P220
[10]  
BHATHAL PS, 1991, HEPATOLOGY, V14, pA106