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. 2021 Nov 20;46(4):305–321. doi: 10.1584/jpestics.D21-028

Table 3. In vitro metabolism of pesticides in birds.

Pesticidea) Sp.b) Organc) °C Prod) Sube) Cofactorf) MRg) Ref.
Lindane CH L (c) 37.5 na 3.8 ± GSH R2 109
Aldrin CH L (S9) 41 na na NADPH O3 110
DDT FP L (ts) 41.5 0.1* 11 ± GSH R1/2 111
Methoxychlor JQ L (ts) 39 na* 5 none O1, C1 112
PCPMs CH L (m) 37 62 2.5 GSH C3 86
Carbaryl JQ L,K (m,c,S9) 37 4 1 NADPH, GSH O1, H2, C1/2/3 91
Aldicarb CH L (m) rt 3 50 NADPH O4 66
Phenmedipham CH B 37 na 82 none H2 81
Trichlorfon CH L (c) 37.5 na 73 none C3 113
Tetrachlorvinphos CH L (c) 37.5 na 0.3 GSH R2/3, H5, C3 87
Diazinon TU L (ts) 37 0.4* 66 NADPH O1/5, M3 64
Parathion CH L,K (ts) 37 10* 0.5 NADPH R4 67
Fenitrothion CH L (m,c) 37 na 70 NADPH, GSH O1/5, H5, C3 85
NMC JQ L (m,c) 37 10 0.5 UDPGA, PAPS C1/2 102
EPN CH L (m) 37 0.5–5 0.5 NADPH O5, H5 114
Chlortoluron JQ L,K (S9) 37 4 1 NADPH, GSH O1 91
Diflubenzuron CH L (m) 37 3–5 21 NADPH O2, H2 115
Cypermethrin JQ L,I (S9),B 42 na 10 NADPH,UDPGA O1/2, H1, C1 82
Deltamethrin CH L (m,c) 37 0.2* 6.5 ± NADPH O1/2, R3, H1 116
Fenvalerate JQ L (h) 42 1 1.8 none O1/2, H1, M3 117
PBacid CH L,K,I (m) 42 0.1* 0.3 NADPH O2, H3 118,119
Fenproximate JQ L (S9) 25 na 0.1 NADPH O1/2, M1 120
Kresoxim-methyl CH L (h) 37 2–5 0.1 none O1/2, H1/3 121
Atrazine CH L (c) 37.5 na 0.8 GSH O1, H6 122
Terbutryn CH L (m, S9) 37 1–5 0.1 ± NADPH, GSH O1, H6** 123
Warfarine CH L (m,c) 41 1 0.4 NADPH O2, R3 68

a) PCPMs, pentachlorophenyl methyl sulfoxide and sulfone; NMC, 3-methyl-4-nitrophenol (metabolite of fenitrothion); PBacid, 3-phenoxybenzoic acid (metabolite of several pyrethroids). b) Tested species. CH, chicken; FP, feral pigeon; JQ, Japanese quail; TU, turkey. c) L, liver; K, kidney; I, intestine; B, blood plasma. The words in the parentheses mean the microsomal (m), cytosolic (c), post-mitochondrial (S9) fractions, hepatocytes (h), and tissue slices or homogenates (ts), respectively. d) Protein concentration of each fraction in mg/ml; *, in g tissue/ml; , in 106 cells/ml. e) Pesticide concentration in μM. , in mM. f) NADPH, nicotinamide adenine dinucleotide phosphate; UDPGA, uridine 5′-diphosphoglucuronic acid; GSH, reduced glutathione; PAPS, phosphoadenosyl phosphosulfate. g) Metabolic reactions (see Table 2); **, hydrolytic dethiomethylation. na, not available. r.t., room temperature.