Monascus species have the unique ability to economically produce many secondary metabolites. However, most metabolic regulation processes in the production of secondary metabolites in Monascus remain unclear. We found that the translational inhibitor cycloheximide induced different expression patterns between the monascorubrin pigment production and the growth in Monascus pilosus. Here, we used the proteomic approach of two-dimensional gel electrophoresis, matrix-assisted laser desorption ionization time-of-flight/time-of-flight liquid chromatography-mass spectrometry (MALDI-TOF/TOF LC-MS), and tandem mass spectrometry (MS/MS) to identify the intracellular and mitochondrial proteins of M. pilosus between the cycloheximide treatment and the control. These results revealed that the cycloheximide-induced down-regulated proteins were involved in transcriptional regulation, peptide synthesis, and other metabolic processes, such as methylation of secondary metabolites. In contrast, the energy-related proteins, such as the transcriptional regulator rosAr and 1,4-alpha-glucan branching enzyme, were up-regulated as compared to the control.
Erinacine A, derived from the mycelia of Hericium erinaceus, has attracted much attention due to its neuroprotective properties. However, very few studies have been conducted on the bioavailability, tissue distribution, and protein binding of erinacine A. This study aimed to investigate the bioavailability, tissue distribution, and protein binding of erinacine A in Sprague-Dawley rats. After oral administration (po) and intravenous administration (iv) of 2.381 g/kg BW of the H. erinaceus mycelia extract (equivalent to 50 mg/kg BW of erinacine A) and 5 mg/kg BW of erinacine A, respectively, the absolute bioavailability of erinacine A was estimated as 24.39%. Erinacine A was detected in brain at 1 h after oral dosing and reached the peak at 8 h. Protein binding assay showed unbound erinacine A fractions in brain to blood ratio is close to unity, supporting passive diffusion as the dominating transport. Feces was the major route for the elimination of erinacine A. This study is the first to show that erinacine A can penetrate the blood-brain barrier of rats by the means of passive diffusion and thus support the development of H. erinaceus mycelia for the improvement of neurohealth.
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