Searchable abstracts of presentations at key conferences in endocrinology

ea0084ps2-09-78 | Thyroid Hormone ACTION | ETA2022

Synthetic analogs of 3-iodothyronamine (T1AM) prevent β-amyloid neurotoxicity in an in vitro model of alzheimer’s disease (AD)

Polini Beatrice , Ricardi Caterina , Carnicelli Vittoria , Tosi Paolo , Bacci Andrea , Rapposelli Simona , Zucchi Riccardo , Chiellini Grazia

We have already reported that synthetic analogs of 3-iodothyronamine (T1AM), a naturally occurring thyroid hormone derivative, share a pleiotropic activity with the endogenous parent compound, including autophagic flux promotion (ATG), neuroprotection, and metabolic reprogramming. Our study aimed to determine whether the T1AM lead analog SG2 and its derivatives SG22 and SG23, developed as prodrugs of SG2, can protect human glioblastoma U87 MG cells from the toxic effects induc...

ea0049gp223 | Thyroid 3 | ECE2017

Endogenous TH metabolite 3-iodothyronamine (T1AM) and synthetic thyronamine-like analogues SG-1 and SG-2 induce autophagy in human glioblastoma cells (U-87MG)

Bellusci Lorenza , Sabatini Martina , Nesi Giulia , Rapposelli Simona , Rossi Leonardo , Lenzi Paola , Fornai Francesco , Zucchi Riccardo , Chiellini Grazia

Endogenous TH metabolite 3-iodothyronamine (T1AM) and recently developed thyronamine-like synthetic analogues SG1 and SG2 have emerged as neuroprotective agents. Autophagy has proved to be an effective therapeutic approach for neurodegenerative diseases. Therefore we investigated whether these compounds can induce autophagy in human glioblastoma cells (U-87MG).Cultured U-87MG cells were initially treated with 1 μM T1AM, SG-1, SG-2 or vehicle for 30&...