Table 5.
(Poly)phenol Metabolite 1 | Strain/Start of Exposure | Model without Intervention | Dose and Time | Mechanistic Evidence | Ref. |
---|---|---|---|---|---|
Benzoic Acids | |||||
Benzoic Acid | AB/2 dpf | Neuronal Teratogenesis | 0.07; 0.7; 3.47; 6.94 mM Sodium Benzoate in the Water Medium for 24 h 2 | ↓ Tactile Sensitivity and ↓ Larvae Mobility (6.94 mM) ↑ Misalignment of Muscle Fibers (6.94 mM) Defects on Motor Axons and Neuromuscular Junctions ↑ Axonal Projections and AchR Clusters (post–synapses; >69.4 µM) |
[147] |
AB/2 hpf | DA System/Neuronal Development | 0.28; 0.94 mM SB in the Water Medium for up to 3 dpf 2 | ↓ TH and DAT Expression in DA Neurons | [148] | |
AB/2 hpf | Locomotor Activity | 0.14; 0.28 mM SB in the Water Medium for 3 Days 2 | ↓ Locomotor Activity | [148] | |
AB/5 hpf | Anxiety–Like Larval Behavior (Thigmotaxis) | 0.35 mM SB in E3 Medium for 72 h 2 | Thigmotaxis ↓ GSR Expression |
[149] | |
3,4,5—Trihydroxybenzoic Acid Gallic Acid) | AB/72 hpf | Neuronal Hyperactivity/Motoneuron Hyperexcitability | 0.30 mM in E3 Medium for 30 min 3 | ↓ Glutamate and GABA ↑ fosab Expression in Distinct Areas of the Brain (Forebrain, Olfactory Bulbs and Pallial Area) ↑ Locomotor Function: Hyperactivity |
[142] |
n.d/ 4–6 Month |
Neurochemical Content Changes | 29.4, 58.8, 117.60 µM in the Water Medium for 24 and 48 h 3 | ↓ Sulfhydryl Content (117.6 µM) ↓ TBA–RS (117.6 µM) ↓ DCFH Oxidation (117.6 µM) ↓ AChE Activity (117.6 µM) = ChAT activity, Nitrates and Nitrites (117.6 µM) ↑ SOD Activity (29.4–58.8 µM) ↑ Catalase Activity (29.4–117.6 µM) = [GSH] (29.4–117.6 µM) |
[143] |
dpf—days post-fertilization; hpf—hours post-fertilization; Wild—Type Lines: AB/Tuebingen; E3—Zebrafish embryonic medium; DA—Dopaminergic; n.d—non–defined; SB—sodium benzoate; AchR—acetylcholine receptor; TH—Tyrosine hydroxylase; DAT—dopamine transporter; GSR—Glutathione reductase; TBA–RS—thiobarbituric acid–reactive species; DCFH—2′,7′—dichlorofluorescein; AChE—acetylcholinesterase; ChAT—choline acetyltransferase; GSH—glutathione 1 (Poly)phenol metabolites are named accordingly the recommendations recently published [32], however the name cited in the original publications where the effect is described is indicated in brackets. 2 Converted from mg·L−1 to µM using molecular mass of 144.105 g·mol−1. 3 Converted from mg·L−1 to µM using molecular mass of 170.12 g·mol−1. ↑—increased ↓—decreased.