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. 2006 Nov;55(11):1606–1616. doi: 10.1136/gut.2005.076778

Table 3 Culture growth of activated human hepatic stellate cells was determined using [3H] thymidine incorporation.

Compound Pharmacological activity Proliferation index
Serum free media (SF) 100 (00)
SF+DPDPE δ1 receptor agonist 89 (9)
SF+deltorphin II δ2 receptor agonist 127 (49)
SF+PDGF‐BB Growth factor 398 (88)*
Fetal calf serum (SP) Growth factor 1524 (1193)*
SP+DPDPE Growth factor/δ1 receptor agonist 1065 (863)*
SP+deltorphin II Growth factor/δ2 receptor agonist 1316 (913)*
SP+PDGF‐BB Growth factor/growth factor 1828 (1432)*

Following 24 hours of serum starvation, cells were cultured for an additional 16 hours in serum supplemented (16%) or serum free media in the presence of DPDPE or deltorphin II (selective δ1 and δ2 receptor agonists, respectively) or recombinant human platelet derived growth factor (PDGF‐BB) prior to addition of [methyl‐3H] thymidine. Cells were incubated for a further 24 hours before washing with Hanks balanced salt solution and fixing.

Data are presented as mean (SEM) of three double experiments (n = 3).

*p<0.05 compared with serum free group.