Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.6.3.44 (
P-glycoprotein
)
13,344
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
P-glycoprotein
(
P-gp
) is a 170-kDa membrane-bound glycoprotein shown to efflux a wide variety of chemicals, such as chemotherapeutic agents and carcinogens. Experiments were conducted using B16/F10 murine melanoma cells transfected with the human MDR1 gene (B16/hMDR1 cells), which codes for
P-gp
, to determine whether this transporter may contribute to the cellular efflux of some pesticides. Thirty-eight pesticides representing several classes of compounds were evaluated for their potential to bind to
P-gp
, as measured by the inhibition of efflux of the
P-gp
substrate doxorubicin.
Carbamate
and pyrethroid insecticides exhibited little interaction with
P-gp
, while many of the organophosphorus and organochlorine pesticides significantly inhibited the efflux of doxorubicin. Pesticides that significantly inhibited the efflux of doxorubicin were then assessed for
P-gp
-mediated efflux. One pesticide, endosulfan, exhibited slight though significant transport mediated by
P-gp
. Competition experiments performed with the
P-glycoprotein
ligand [3H]azidopine demonstrated that the
P-gp
inhibitory pesticides bound to
P-gp
. Both lipophilicity and molecular mass were major physical/chemical determinants in dictating pesticide binding to
P-gp
, with optimum binding occurring with compounds having a log Kow value of 3.6-4.5 and a molecular weight of 391-490 Da. The transport substrate endosulfan possessed optimal binding characteristics. These results demonstrated that many pesticides are capable of binding to
P-gp
; however, binding does not infer transport.
...
PMID:Interaction of structurally diverse pesticides with the human MDR1 gene product P-glycoprotein. 891 2