Reto Erni's research while affiliated with ETH Zurich and other places
What is this page?
This page lists the scientific contributions of an author, who either does not have a ResearchGate profile, or has not yet added these contributions to their profile.
It was automatically created by ResearchGate to create a record of this author's body of work. We create such pages to advance our goal of creating and maintaining the most comprehensive scientific repository possible. In doing so, we process publicly available (personal) data relating to the author as a member of the scientific community.
If you're a ResearchGate member, you can follow this page to keep up with this author's work.
If you are this author, and you don't want us to display this page anymore, please let us know.
It was automatically created by ResearchGate to create a record of this author's body of work. We create such pages to advance our goal of creating and maintaining the most comprehensive scientific repository possible. In doing so, we process publicly available (personal) data relating to the author as a member of the scientific community.
If you're a ResearchGate member, you can follow this page to keep up with this author's work.
If you are this author, and you don't want us to display this page anymore, please let us know.
Publications (4)
Aging is impacted by interventions across species, often converging on metabolic pathways. Transcription factors regulate longevity yet approaches for their pharmacological modulation to exert geroprotection remain sparse. We show that increased expression of the transcription factor Grainyhead 1 (GRH-1) promotes lifespan and pathogen resistance in...
The cis-stereoisomers of Δ⁹-THC [(−)-3 and (+)-3] were identified and quantified in a series of low-THC-containing varieties of Cannabis sativa registered in Europe as fiber hemp and in research accessions of cannabis. While Δ⁹-cis-THC (3) occurs in cannabis fiber hemp in the concentration range of (−)-Δ⁹-trans-THC [(−)-1], it was undetectable in a...
Phytochemical studies on the liverwort Radula genus have previously identified the bibenzyl (−)- cis -perrottetinene ( cis -PET), which structurally resembles (−)-Δ ⁹ - trans -tetrahydrocannabinol (Δ ⁹ - trans -THC) from Cannabis sativa L. Radula preparations are sold as cannabinoid-like legal high on the internet, even though pharmacological data...
Citations
... the opposite phenotype of high-level overexpression; we recently have shown that limited overexpression of Grainyhead 1 (ghr-1) following transgene bombardment in C. elegans promotes longevity, whereas high-level overexpression of the same transgene shortens lifespan (49). ...
... This justifies why THC (and other molecules with partial or full agonistic activity on CB1, including the weak psychoactive D9-cis-THC enantiomer, recently demonstrated to occur naturally in Hemp-derived nutraceuticals, both phytocannabinoids and non-cannabinoids, with potential effects on the gastrointestinal tract and the brain-gut axis. (Schafroth et al., 2021), should be absent (or at low, non-psychotropic levels) in hemp-derived food products, as a minimum health safety requirement. With antagonistic or negative allosteric activity on CB1 receptors as an outstanding feature, the pharmacology of CBD is very complex (summarized in Table 5) and underlies its broad biological activities, including neuroprotection, analgesia, antiinflammatory and immune-modulating effects, anxiolytic, spasmolytic, anticonvulsant and antipsychotic effects, mood stabilization, and normalization of sleep disorders, just to name a few (Kicman and Toczek, 2020;Mlost et al., 2020;Britch et al., 2021;Franco et al., 2021;Vitale et al., 2021). ...
... Representative analogs from each of these three legends, compounds 5, 11, 13, 14 and 17, were selected, based on IC 50 values of 3.0 µg/mL or <3.0 µg/mL as a cut-off value against MRSA for MIC determination. Among the analogous of stemofuran A (1-5 and 17), pinosylvin (6)(7)(8)(9)(10)(11)(12)(13)(14), and resveratrol (15,16), compound 5, 11, and 17 exhibited the most potent activity against MRSA ATCC 1708, with IC 50 /MIC values of 1.18/2.50 µg/mL, 0.91/1.25 µg/mL, and 0.95/1.25 µg/mL, respectively. ...