Database Query Results : Ginkgo biloba, ,

Gb, Ginkgo biloba: Click to Expand ⟱
Features:
Ginkgo biloba from an ancient tree.
-Ginkgo can inhibit platelet aggregation

-Scavenges free radicals; reduces oxidative stress in neuronal cells -Suppresses pro-inflammatory cytokines (e.g., TNF-α, IL-1β).
-Enhances microcirculation and oxygen delivery to brain tissues.
-Reduces plaque formation and associated neurotoxicity.
-May improve memory, attention, and processing speed in early-stage AD.




Scientific Papers found: Click to Expand⟱
1117- Gb,    Ginkgobiloba leaf extract mitigates cisplatin-induced chronic renal interstitial fibrosis by inhibiting the epithelial-mesenchymal transition of renal tubular epithelial cells mediated by the Smad3/TGF-β1 and Smad3/p38 MAPK pathways
- vitro+vivo, Kidney, HK-2
α-SMA↓, COL1↓, TGF-β↓, SMAD2↓, SMAD3↓, p‑SMAD2↓, p‑SMAD3↓, p38↓, p‑p38↓, Vim↓, TIMP1↓, CTGF↓, E-cadherin↑, MMP1:TIMP1↑,
1186- Gb,    Ginkgolic acid suppresses the development of pancreatic cancer by inhibiting pathways driving lipogenesis
- in-vitro, PC, NA - in-vitro, Nor, HUVECs - in-vivo, PC, NA
tumCV↓, *toxicity∅, TumCMig↓, TumCI↓, Apoptosis↑, AMPK↑, lipoGen↓, ACC↓, FASN↓,
1187- Gb,    Ginkgolic Acid C 17:1, Derived from Ginkgo biloba Leaves, Suppresses Constitutive and Inducible STAT3 Activation through Induction of PTEN and SHP-1 Tyrosine Phosphatase
- in-vitro, Melanoma, U251 - in-vitro, Melanoma, MM.1S
STAT3↓, PTEN↑, Apoptosis↑, PTPN6↑,
1188- Gb,    The potential of Ginkgo biloba in the treatment of human diseases and the relationship to Nrf2-mediated antioxidant protection
- Review, NA, NA
*NRF2↑, *ROS↓,
1189- Gb,    New insight into the mechanisms of Ginkgo biloba leaves in the treatment of cancer
- Review, NA, NA
Apoptosis↑, TumCP↓, TumCI↓, TumCMig↓, Inflam↓, antiOx↑, angioG↓,
1190- Gb,    Extract of Ginkgo biloba exacerbates liver metastasis in a mouse colon cancer Xenograft model
- in-vivo, CRC, SW-620
TumMeta↑, Ki-67↑,
3721- Gb,    Ginkgo biloba Extract in Alzheimer’s Disease: From Action Mechanisms to Medical Practice
- Review, AD, NA
*antiOx↑, *ROS↓, *SOD↑, *Catalase↑, *GSR↑, *MMP↑, *Inflam↓, *↓, *memory↑, *Dose↝, *BBB↑, *neuroP↑,
3722- Gb,    Alzheimer's disease: Research summaries – Do Ginkgo products help?
- Review, AD, NA
*memory↑, *AntiAg↑,
3723- Gb,    Can We Use Ginkgo biloba Extract to Treat Alzheimer’s Disease? Lessons from Preclinical and Clinical Studies
- Review, AD, NA
*memory↑, *antiOx↑, *Casp3↓, *APP↓, *AChE↓, *↓, *5HT↑, *SOD↓, *MDA↓, *NO↓, *GSH↑, *Bcl-2↑, *BAX↑, *TNF-α↓, *IL1β↑, *iNOS↓, *IL10↓, *p‑tau↓, *ROS↓, *MAOB↓, *cognitive↑, *neuroP↑, *Apoptosis↓,
4244- Gb,    Effects of Six-Week Ginkgo biloba Supplementation on Aerobic Performance, Blood Pro/Antioxidant Balance, and Serum Brain-Derived Neurotrophic Factor in Physically Active Men
- Human, Nor, NA
*BDNF∅,
4245- Gb,    Standardized extract of Ginkgo biloba enhances memory persistence over time
- in-vivo, NA, NA
*memory↑, *BDNF↑,

* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 11

Pathway results for Effect on Normal Cells:


Redox & Oxidative Stress

antiOx↑, 2,   Catalase↑, 1,   GSH↑, 1,   GSR↑, 1,   MDA↓, 1,   NRF2↑, 1,   ROS↓, 3,   SOD↓, 1,   SOD↑, 1,  

Mitochondria & Bioenergetics ATP production, membrane potential, mitochondrial signaling, and dynamics (fission, fusion, mitophagy). It includes mitochondrial contributions to apoptosis, metabolism, and redox signaling. Mitochondrial dysfunction is a core driver of cancer metabolism, neurodegeneration, and age-related decline." style="cursor:help;color:#555;font-weight:normal;">ⓘ

MMP↑, 1,  

Cell Death

Apoptosis↓, 1,   BAX↑, 1,   Bcl-2↑, 1,   Casp3↓, 1,   iNOS↓, 1,  

Migration

AntiAg↑, 1,   APP↓, 1,  

Angiogenesis & Vasculature

NO↓, 1,  

Barriers & Transport BBB, epithelial layers), membrane transporters, ion channels, and water channels. It governs permeability, cellular uptake/efflux, tissue protection, and drug access to target compartments." style="cursor:help;color:#555;font-weight:normal;">ⓘ

BBB↑, 1,  

Immune & Inflammatory Signaling Inflammation group includes innate and adaptive immune pathways, cytokines, chemokines, pattern-recognition receptors, complement, and inflammasomes. It regulates host defense, tumor immunity, neuroinflammation, and chronic inflammatory disease processes." style="cursor:help;color:#555;font-weight:normal;">ⓘ

IL10↓, 1,   IL1β↑, 1,   Inflam↓, 1,   TNF-α↓, 1,  

Synaptic & Neurotransmission memory, and neuronal survival, and is especially relevant to Alzheimer’s and other neurodegenerative diseases." style="cursor:help;color:#555;font-weight:normal;">ⓘ

5HT↑, 1,   AChE↓, 1,   BDNF↑, 1,   BDNF∅, 1,   p‑tau↓, 1,  

Protein Aggregation tau biology, proteolytic processing, and aggregate toxicity. It captures molecular features specific to neurodegenerative pathology but remains extensible to other aggregation disorders." style="cursor:help;color:#555;font-weight:normal;">ⓘ

↓, 2,   MAOB↓, 1,  

Drug Metabolism & Resistance

Dose↝, 1,  

Functional Outcomes cognitive performance, toxicity, and organism-level effects. It is intentionally mechanism-agnostic and anchors molecular data to real-world biological impact." style="cursor:help;color:#555;font-weight:normal;">ⓘ

cognitive↑, 1,   memory↑, 4,   neuroP↑, 2,   toxicity∅, 1,  
Total Targets: 35

Query results interpretion may depend on "conditions" listed in the research papers.
Such Conditions may include : 
  -low or high Dose
  -format for product, such as nano of lipid formations
  -different cell line effects
  -synergies with other products 
  -if effect was for normal or cancerous cells
Filter Conditions: Pro/AntiFlg:%  IllCat:%  CanType:%  Cells:%  prod#:89  Target#:%  State#:%  Dir#:%
wNotes=0 sortOrder:rid,rpid

 

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