Neurogenic Potential of Acacia oerfota: Evaluating the Effects of DMT-Rich Extract on PC12 Cells
Narges Ghasemi Lakeh, Mona Farhadi, Fatemeh Siadat
Thrita December 31, 2024 DOI: 10.5812/thrita-161580 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | In vitro cell study Peer reviewed |
|---|---|
| Population | PC12 cells |
| Dose | 0.01 to 1.6 µg/mL |
| Duration | 24 and 48 hours |
| Measures | MTT assay, Sub-G1 assay, reactive oxygen species (ROS) levels, BDNF gene expression |
| Topics | DMT |
| Key points | Acacia oerfota leaf extract showed dose- and time-dependent cytotoxicity at 0.8 and 1.6 µg/mL and increased reactive oxygen species at 0.4 and 0.8 µg/mL, with no apoptosis detected. BDNF gene expression was significantly upregulated at 0.4 µg/mL, which the authors suggest may indicate neurogenic potential. |
Abstract
Background: Acacia species, including Acacia oerfota, are rich in bioactive compounds such as N,N-dimethyltryptamine (DMT), known for its psychoactive properties. Recent studies suggest that low concentrations of DMT may promote neurogenesis and brain plasticity, offering therapeutic potential for neurodegenerative diseases like Alzheimer’s and depression.
Methods: A hydroalcoholic extract of A. oerfota leaves was prepared. PC12 cells were cultured and treated with extract concentrations ranging from 0.01 to 1.6 µg/mL. Cytotoxicity was assessed using the MTT assay at 24 and 48 hours. The Sub-G1 assay evaluated apoptosis, while reactive oxygen species (ROS) levels were measured. Brain-derived neurotrophic factor (BDNF) gene expression was analyzed to assess neurogenic potential.
Results: Significant cytotoxic effects were observed at 0.8 and 1.6 µg/mL concentrations, with effects being dose- and time-dependent. At 48 hours, 0.8 µg/mL showed significant cytotoxicity (P ≤ 0.05). The ROS levels increased at 0.4 and 0.8 µg/mL, with significance at 0.8 µg/mL. No apoptosis was detected in any treatment group. Notably, BDNF gene expression was significantly upregulated at 0.4 µg/mL compared to the control.
Conclusions: Acacia oerfota extract may enhance neurogenesis in a concentration- and time-dependent manner. Further research focusing on DMT’s role in promoting neurogenesis is warranted.
Comparable studies
Other preclinical and animal studies on DMT, most cited first.
| Study | Year | Design | Participants |
|---|---|---|---|
| The Hallucinogen N,N -Dimethyltryptamine (DMT) Is an Endogenous Sigma-1 Receptor Regulator Mice and cell lines | 2009 | Experimental study | |
| Correlation between the potency of hallucinogens in the mouse head-twitch response assay and their behavioral and subjective effects in other species. C57BL/6J mice | 2020 | Experimental study with dose-response experiments | |
| Psychedelic N,N-dimethyltryptamine and 5-methoxy-N,N-dimethyltryptamine modulate innate and adaptive inflammatory responses through the sigma-1 receptor of human monocyte-derived dendritic cells. Human primary monocyte-derived dendritic cells | 2014 | In vitro study | |
| Inhibitory effect of chlorpromazine on the syndrome of hyperactivity produced by l‐tryptophan or 5‐methoxy‐N,N‐dimethyltryptamine in rats treated with a monoamine oxidase inhibitor Rats | 1971 | Experimental study | |
| Effects of N,N-Dimethyltryptamine on Rat Behaviors Relevant to Anxiety and Depression Adult male Sprague-Dawley rats | 2018 | Experimental study |
Citations in the library
Cites 6
- Monoamine oxidase inhibitors in South American hallucinogenic plants: Tryptamine and β-carboline constituents of Ayahuasca Journal of Ethnopharmacology April 1, 1984
- N, N-Dimethyltryptamine (DMT), an Endogenous Hallucinogen: Past, Present, and Future Research to Determine Its Role and Function Frontiers in Neuroscience August 6, 2018
- Psychedelic Drugs in Biomedicine TIPS - Trends in Pharmacological Sciences September 22, 2017
- N,N-dimethyltryptamine reduces infarct size and improves functional recovery following transient focal brain ischemia in rats Experimental Neurology February 14, 2020
- N,N-dimethyltryptamine Prevents Renal Ischemia-Reperfusion Injury in a Rat Model. Transplantation Proceedings May 1, 2019
and 1 more in the library