NATURAL-PRODUCTS AS PROBES FOR NEW DRUG TARGET IDENTIFICATION

被引:13
作者
EVANS, FJ
机构
[1] Department of Pharmacognosy, The School of Pharmacy, University of London, London, WC1NIAX
关键词
D O I
10.1016/0378-8741(91)90107-O
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
One traditional aspect of natural products in medical research has been their use in the identification and investigation of the physiological/pathological role of receptors and enzymes as possible targets for drug design programmes. Classical examples of this function of natural products in drug research can be seen in the investigation of the cholinergic system. For example, the importance of alkaloids such as nicotine, physostigmine and curare for research into the nicotinic receptor and muscarine, pilocarpine and the tropane alkaloids on the muscarinic receptor. On binding of a ligand to its cell surface membrane receptor and prior to a physiological/pharmacological response two mechanisms are currently know to be involved in membrane signal transductance. In the majority of cases signal transductance involves the direct opening of an ion channel, for example sodium ion influx, but in the majority of cases involves stimulation of a family of G-proteins and subsequent activation of second messenger systems. For example, the cyclic-AMP/adenylate cyclase system and the phosphoinositol cycle. In this communication, the part played currently by the tumour-promoting and pro-inflammatory phorbol esters from the plant family Euphorbiaceae in furthering our understanding of the role of a group of related kinases from one arm of the phosphoinositol cycle as a signal transduction pathway will be illustrated. The possibilities of using these new receptors as targets for future drug development will also be described.
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页码:91 / 101
页数:11
相关论文
共 21 条
[1]   THE ACTIVATION OF PROTEIN-KINASE-C BY DAPHNANE, INGENANE AND TIGLIANE DITERPENOID ESTERS [J].
AITKEN, A .
BOTANICAL JOURNAL OF THE LINNEAN SOCIETY, 1987, 94 (1-2) :247-263
[2]   TUMOR-PROMOTING AND HYPERPLASTIC EFFECTS OF PHORBOL AND DAPHNANE ESTERS IN CD-1 MOUSE SKIN AND A SYNERGISTIC EFFECT OF CALCIUM IONOPHORE WITH THE NON-PROMOTING ACTIVATOR OF PROTEIN KINASE-C, SAPINTOXIN-A [J].
BROOKS, G ;
EVANS, AT ;
AITKEN, A ;
EVANS, FJ .
CARCINOGENESIS, 1989, 10 (02) :283-288
[3]   THE STIMULATION OF PHOSPHORYLATION OF INTRACELLULAR PROTEINS IN GH3-RAT PITUITARY-TUMOR CELLS BY PHORBOL ESTERS OF DISTINCT BIOLOGICAL-ACTIVITY [J].
BROOKS, SF ;
EVANS, FJ ;
AITKEN, A .
FEBS LETTERS, 1987, 224 (01) :109-116
[4]   PLATELET PROTEIN-PHOSPHORYLATION AND PROTEIN KINASE-C ACTIVATION BY PHORBOL ESTERS WITH DIFFERENT BIOLOGICAL-ACTIVITY AND A NOVEL SYNERGISTIC RESPONSE WITH CA-2+ IONOPHORE [J].
BROOKS, SF ;
GORDGE, PC ;
TOKER, A ;
EVANS, AT ;
EVANS, FJ ;
AITKEN, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 188 (02) :431-437
[5]  
DREIDGER PE, 1980, P NATL ACAD SCI USA, V77, P567
[6]  
DRUMMOND AH, 1987, PHYTOTHER RES, V1, P1
[7]  
Ellis C. A., 1987, PHYTOTHER RES, V1, P187
[8]   TPA AND RESINIFERATOXIN-MEDIATED ACTIVATION OF NADPH-OXIDASE - A POSSIBLE ROLE FOR RX-KINASE AUGMENTATION OF PKC [J].
EVANS, AT ;
SHARMA, P ;
RYVES, WJ ;
EVANS, FJ .
FEBS LETTERS, 1990, 267 (02) :253-256
[9]  
Evans F. J., 1983, PROGR CHEM ORGANIC N, V44, P1
[10]   ACTIVITY CORRELATIONS IN THE PHORBOL ESTER SERIES [J].
EVANS, FJ ;
EDWARDS, MC .
BOTANICAL JOURNAL OF THE LINNEAN SOCIETY, 1987, 94 (1-2) :231-246