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. 2021 Mar 18;10(6):1253. doi: 10.3390/jcm10061253

Table 2.

Drugs used in experimental models for ex-vivo defatting of steatotic livers.

Model n Perfusion Length of Perfusion (hours) Defatting Agents Main Outcomes
Nagrath et al., 2009 [18] rat 7 NMP 3 combination of visfatin, forskolin, hypericin and nuclear receptor ligands (GW7, GW5, scoparone) decrease of TG rate
improvement of bile production
Liu et al.,
2013 [25]
rat NA SNMP 6 combination of amino acids, visfatin, forskolin, hypericin and nuclear receptor ligands (GW7, GW5, scoparone) higher rate of TG (non significance)
Raigani et al., 2020 [26] rat 6 NMP 6 combination of amino acids, visfatin, forskolin, hypericin and nuclear receptor ligands (GW7, GW5, scoparone) decrease of pro inflammatory markers (NF- κB, TNF-α, IL-6)
decrease of pro-apoptotic markers (CASP3, CD95)
decrease of combined VLDL/LDL level
Taba Taba Vakili et al., 2016 [27] mice 4 NMP 4 glial cell
line–derived neurotrophic factor
reduction of TG content in liver
no liver damage (no increase of apoptosis)
Banan et al.,
2016 [31]
human discarded livers 2 NMP 8 L-carnithine and exendin-4 decrease of TG and LDL level in the perfusate
reduction of Mas
Boteon et al.,
2019 [32]
human livers discarded 5 NMP 12 combination of L-carnithine, visfatin, forskolin, hypericin and nuclear receptor ligands (GW7, GW5, scoparone) decrease of T-TG level
decrease of MaS
increase of P-TG level
higher bile production

LDL: low-density lipoprotein; MaS: macrovesicular steatosis; NMP: normothermic perfusion; P-TG: SNMP: subnormothermic perfusion; TG: triglycerides; T:TG: tissue-TG; VLDL: very low-density lipoprotein.