Male C57BL/6 mice |
25 and 50 mg/kg/day |
ELISA |
TNFα↓, IL-6↓, IL-10↓, ROS production↓, SOD↓, NF-κB↓ |
12 h |
Lycopene, via reducing oxidative stress and inflammation, was effective in preventing liver damage induced by long-term CS exposure |
(Rocha et al. 2021) |
Male Sprague–Dawley rats |
5 mg/kg BW |
ELISA |
↑CAT, ↑SOD, ↑GPx, TNF-α↓, CRP↓ |
10 weeks |
In T2DM rats, lycopene could reduce oxidative stress by reducing glucose and lipid peroxidation, as well as reduce inflammatory events |
(Zheng et al. 2019) |
STZ-induced diabetic Wistar rats |
10 or 20 mg/kg/BW |
ELISA |
SOD↑, GSH-Px↑, MDA↓ |
10 weeks |
In diabetic rats, lycopene enhances glycolipid metabolism by reducing oxidative stress |
(Yin et al. 2019) |
Wistar male rats |
4 mg/kg |
ELISA, spectrophotometer |
MDA↓, TOS↓, NF-κB↓, TNFα↓ |
3 months |
Lycopene can alleviate inflammatory responses by reducing oxidative stress |
(Icel et al. 2019) |
Adult male Wistar albino rats |
50 mg/kg |
ELISA, spectrophotometer, qPCR |
TNFα↓, iNOS↓, MPO↓, NO↓, GSH↑, |
10 days |
Lycopene prior treatment proved anti-inflammatory and antioxidant effects against acute pancreatitis (AP) rat |
(El-Ashmawy et al. 2018) |
Female Wistar–Albino rats |
4 mg/kg/BW |
Spectrophotometer |
MDA↓, CAT↑, SOD↑, GPx↑, and GST↑ |
28 days |
Lycopene possesses antioxidant properties that protect ovarian tissue against the toxicity of diabetic furans and non-diabetic |
(Uçar and Pandir 2017) |
Weanling ICR Male mice |
60 and 1 mg/kg |
ELISA, Immunoblotting |
IL-1β↓, TNF-α↓, IL-6↓, HO-1↓ |
6–24 h |
Lycopene can reduce LPS-induced inflammation and depression-like behavior by inhibiting the production of pro-inflammatory cytokines |
(Zhang et al. 2016) |
Male C57BL/6 mice |
50 or 25 mg/kg/day |
ELISA |
IL-10↓, IFN-γ↓, TNF-α↓, SOD↑, CAT↑, GSH↑ |
60 days |
lycopene has anti-inflammatory and antioxidant properties; it may be a promising novel treatment for acute lung inflammation and emphysema in mice exposed to CS |
(Campos et al. 2019) |
Sprague–Dawley rats |
25 or 50 mg/kg |
ELISA, Western blotting |
TNF-α↑, IL-1β↑, IL-6↑, and IL-8↑, HO-1↑, COX-2↓ |
14 days |
The anti-inflammatory properties of lycopene may be used as a therapy to protect against spinal cord ischemia/reperfusion injury (SCII) |
(Hua et al. 2019) |
Male mice |
20 mg/kg |
ELISA, Western blotting |
ALT↓, AST↓, TNF-α↓, IL-6↓, MDA ↓, SOD↑, Nrf2↑, COX-2↓, NF-κB↓ |
2 weeks |
Lycopene has been reported to lessen the liver damage brought on by LPS by reducing oxidative stress and inflammatory damage |
(Dong et al. 2019) |
Adult male C57BL/6j mice |
2 μM |
Western blotting, luminex kit |
IL-6↓, MCP-1↓, IL-1β↓, TNFα↓, NF-κB↑ |
24 h |
Lycopene could prevent or reduce the prevalence of obesity-related diseases by reducing the expression of pro-inflammatory cytokines and chemokines in adipose tissues |
(Gouranton et al. 2011) |
Macrophage and adipocyte cells |
0.5–2 µM |
ELISA, Western blot |
↓IL-1β, ↓TNF-α, ↓IL-6, JNK ↑, NF-κB↑ |
24 h |
Lycopene has the potential to disrupt the vicious loop that occurs in adipose tissue between adipocytes and macrophages during obesity |
(Marcotorchino et al. 2012) |
Eight-week-old male C57BL/6 J mice |
Powder |
ELISA |
TNFα↓, IL-6↓, CCL2↓, CCL5↓, MCP-1↓, NF-κB↓, IκB↓, p65↓ |
12 weeks |
Lycopene has beneficial effects on inflammatory responses, obesity, and metabolic disorders |
(Fenni et al. 2017) |
Airway epithelial cells |
2.5 μg/ml |
ELISA |
IL-6↓, IP-10↓, NF-κB↓ |
48 h |
Lycopene may also be effective in reducing rhinovirus-induced airway inflammation |
(Saedisomeolia et al. 2009) |
Sprague–Dawley rats |
2 or 4 mg/kg BW |
ELISA |
ALT ↓, MDA ↓, TNF-α ↓, GSH ↑, HSC activation ↓ |
Orally for 6 weeks |
Lycopene supplementation may help to prevent the progression of steatohepatitis by reducing high-fat diet-induced oxidative stress in the cells |
(Bahcecioglu et al. 2010) |
C57BL/6 mice |
10 or 100 mg/kg |
RT-PCR, spectrophotometer |
CAT ↑, GSH ↑, TBARS ↓, IL1β ↓, Redox imbalance ↓ |
2 weeks |
Lycopene can reduce the oxidative stress caused due to APAP overdose and subsequent liver damage in C57BL/6 mice |
(Bandeira et al. 2017) |
Sprague–Dawley rats |
20 mg/kg diet |
|
SOD ↑, CAT ↑, LDL ↓, GSHPX ↑ |
4 weeks |
Lycopene's potential health advantages against non-alcoholic fatty liver disease (NAFLD) |
(Piña-Zentella et al. 2016) |
Sprague–Dawley rats |
2.5, 5 mg/kg BW |
Spectrophotometer |
CAT ↑, MDA ↓, ALT ↓, AST ↓, LDH ↓ |
|
Lycopene's antioxidant properties protect against ischemia/reperfusion injury |
(Bayramoglu et al. 2015) |
Wistar rats and C57BL/6 mice |
Rats: 1.1 mg/kg Mice: 1.1 mg/kg |
Western blot, real time-PCR |
IL-6 ↓, IL-1β ↓ IFNγ ↓,, Hepatic inflammatory foci ↓ |
4 and 3 weeks |
Dietary lycopene powder can prevent alcohol-induced liver impairment and oxidative damage by inhibiting cytochrome p450 |
(Stice et al. 2015) |
MI mice |
10 mg/kg/day |
Western blot, qPCR |
TNFα ↓, IL-1β↓, NF-κB p65 ↓ |
4 weeks |
Lycopene has been shown to have a cardioprotective effect by inhibiting local myocardial inflammation and apoptosis |
(He et al. 2015) |