TABLE 3.
Beneficial effects of ITCs against pathological hallmarks and their neurotoxicity.
| Plant/Compound | Mechanism of action | Pharmacological effectiveness | Test scale | References |
|---|---|---|---|---|
| Against amyloid beta oligomerization and toxicity | ||||
| Wasabia japonica (6-methylsulfinyl hexyl ITC) | Increased glutathione levels and ROS in hippocampus by Aβ1-42 injection were reduced | Neuroprotection against Aβ1-42 and ameliorates Aβ1-42 induced memory impairments | in-vivo, murine model, induced by intra cerebrovascular injection of Aβ1-42 | Morroni et al. (2018) |
| Indole-3 carbinol (I3C) | High affinity molecular recognition and reduced Aβ fragments by heteromeric interaction | Reduced amyloid production | in-vitro, biochemical method | Cohen et al. (2006) |
| Moringa oleifera extract | Downregulated BACE1 | Decreased Aβ production, rescued cognitive impairment and enhanced the reduced synaptic proteins synapsin, synapsophysin, PSD93 and PSD95 | in-vivo, hyperhomocysteinemia (HHcY) induced AD model | Mahaman et al. (2018) |
| Deactivated calpain by ↓ intracellular Ca 2+, reduced ca2+ signaling and prevent cell death | Decreased cytosolic cysteine protease caplain activity | in-vivo, hyperhomocysteinemia (HHcy) induced rat model (AD like pathology) | Mahaman et al. (2018) | |
| Increased Aβ immunoexpression was significantly abolished, sustained the brain-Zn content | Decreased the aggregation and accumulation of Aβ | in-vivo, ACR induced forty male Sprague Dawley rat treated with MO-ZnONP | Dahran et al. (2023) | |
| Sulforaphane | Increased levels of HSP-70 co-chaperons and CHIP (Aβ metabolism influencers) | Reduced monomeric and polymeric forms of Aβ, but do not affect m-RNA expression, ameliorated memory deficits | in-vivo, triple transgenic mouse model (3×Tg-AD) | Li et al. (2018) |
| Decreased oxidative stress and neuroinflammation (generator of Aβ) | Significantly inhibited Aβ aggregation, ameliorated neurobehavioral deficits peroxidation in brain | in-vivo, 6-month-old PS1V97L transgenic (Tg) mice | Zhang et al. (2015) | |
| Modulated the amyloid expression related markers, inhibited the overexpression of CDK5 in primary neurons | Reduced the Aβ1-42 deposition and related neurotoxicity | in-vivo, TgCRND8 transgenic mice model | Yang et al. (2023) | |
| Inhibited cathepsin-B and caspase-1 dependent NLRP3 inflammasome activation induced by Aβ monomers (1–42) | Reduced Aβ induced neurotoxicity | in-vitro, human THP-1 macrophages like cells | An et al. (2016) | |
| Alleviated several downstream pathological changes including oxidative stress and neuroinflammation | Significantly inhibited the generation of Aβ aggregates promotes spatial learning and memory | in-vivo, PS1V97L transgenic mice model | Hou et al. (2018) | |
| Against tau hyperphosphorylation and toxicity | ||||
| Moringa oleifera extract | Not known | Decreased hyperphosphorylated tau at different sites (S-199, S-404, S-396 and T-231) | in-vivo, hyperhomocysteinemia (HHcy) induced rat model (AD like pathology) | Mahaman et al. (2018) |
| Reduced sensory dysfunction and motor deficits, abolished immunoexpression of phosphorylated tau proteins | Reduced ACR induced neurotoxicity and tau proteins | in-vivo, ACR induced forty male Sprague Dawley rat treated with MO-ZnONP | Dahran et al. (2023) | |
| Sulforaphane | Increased levels of HSP-70 co-chaperons and CHIP (Aβ metabolism influencers) | Reduced protein levels of tau and hyperphosphorylated tau, ameliorated memory deficits | in-vivo, triple transgenic mouse model (3×Tg-AD) | Lee et al. (2014) |
| Suppressed phosphorylation of tau at specific sites, markedly suppressed the CDK5/p25 | Reduced tau protein hyperphosphorylation in the brain and improved synaptic plasticity | in-vivo, TgCRND8 transgenic mice model | Yang et al. (2023) | |
| Altered phosphorylated tau at threonine 181 and serine991/202 distribution within astrocytes | Reduced hyperphosphorylated tau proteins in astrocytes under hypoglycaemic condition | in vitro, embryonic hippocampal rat astrocytes | Komiskey et al. (2022) | |
| Significantly inhibited hyperphosphorylated tau proteins at Ser396, Ser404 and Thr 205 site, enhanced the ration of p-GSK-3β(Ser9)/GSK-3β and p-Akt (Ser473)/Akt in hippocampus | Reduced the accumulation of phosphorylated tau in hippocampus and related toxicity | in-vivo,streptozotocin induced rat model | Yang et al. (2020) | |
| Significantly expressed the NDP52 induced by Nrf2 and facilitated clearance of p-tau proteins | Reduced the phosphorylated tau proteins | in-vivo, C57BL/6J mice model | Jo et al. (2014) | |