RRC ID 63284
著者 Yaku K, Palikhe S, Izumi H, Yoshida T, Hikosaka K, Hayat F, Karim M, Iqbal T, Nitta Y, Sato A, Migaud ME, Ishihara K, Mori H, Nakagawa T.
タイトル BST1 regulates nicotinamide riboside metabolism via its glycohydrolase and base-exchange activities.
ジャーナル Nat Commun
Abstract Nicotinamide riboside (NR) is one of the orally bioavailable NAD+ precursors and has been demonstrated to exhibit beneficial effects against aging and aging-associated diseases. However, the metabolic pathway of NR in vivo is not yet fully understood. Here, we demonstrate that orally administered NR increases NAD+ level via two different pathways. In the early phase, NR was directly absorbed and contributed to NAD+ generation through the NR salvage pathway, while in the late phase, NR was hydrolyzed to nicotinamide (NAM) by bone marrow stromal cell antigen 1 (BST1), and was further metabolized by the gut microbiota to nicotinic acid, contributing to generate NAD+ through the Preiss-Handler pathway. Furthermore, we report BST1 has a base-exchange activity against both NR and nicotinic acid riboside (NAR) to generate NAR and NR, respectively, connecting amidated and deamidated pathways. Thus, we conclude that BST1 plays a dual role as glycohydrolase and base-exchange enzyme during oral NR supplementation.
巻・号 12(1)
ページ 6767
公開日 2021-11-19
DOI 10.1038/s41467-021-27080-3
PII 10.1038/s41467-021-27080-3
PMID 34799586
PMC PMC8604996
MeSH A549 Cells ADP-ribosyl Cyclase / genetics ADP-ribosyl Cyclase / metabolism* Administration, Oral Aging / drug effects Animals Antigens, CD / genetics Antigens, CD / metabolism* Dietary Supplements GPI-Linked Proteins / genetics GPI-Linked Proteins / metabolism Gastrointestinal Microbiome Glycoside Hydrolases / genetics Glycoside Hydrolases / metabolism* Humans Intestinal Mucosa / metabolism Intestinal Mucosa / microbiology Intestine, Small / metabolism Intestine, Small / microbiology Mice Mice, Knockout Niacin / metabolism Niacinamide / administration & dosage Niacinamide / analogs & derivatives* Niacinamide / metabolism Niacinamide / pharmacokinetics Pentosyltransferases / genetics Pentosyltransferases / metabolism Pyridinium Compounds / administration & dosage Pyridinium Compounds / pharmacokinetics*
IF 12.121
リソース情報
ヒト・動物細胞 A549(RCB0098) CACO-2(RCB0988)
実験動物マウス RBRC01462 RBRC02401