Murata Hitoshi, Ogawa Kazuki, Yasui Yu, Ochi Toshiki, Tomonobu Nahoko, Yamamoto Ken-Ichi, Kinoshita Rie, Wada Yoji, Nakamura Hiromichi, Nishibori Masahiro, Sakaguchi Masakiyo
Department of Cell Biology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700-8558, Japan.
Tama Biochemical Co., Ltd., 1-23-3 Nishi-shinjuku, Shinjyuku-ku, Tokyo 160-0023, Japan.
Antioxidants (Basel). 2025 Jun 30;14(7):808. doi: 10.3390/antiox14070808.
Sterile alpha and Toll/interleukin receptor motif-containing protein 1 (SARM1) is a nicotinamide adenine dinucleotide (NAD) hydrolase involved in axonal degeneration and neuronal cell death. SARM1 plays a pivotal role in triggering the neurodegenerative processes that underlie peripheral neuropathies, traumatic brain injury, and neurodegenerative diseases. Importantly, SARM1 knockdown or knockout prevents the degeneration; as a result, SARM1 has been attracting attention as a potent therapeutic target. In recent years, the development of several SARM1 inhibitors derived from synthetic chemical compounds has been reported; however, no dietary ingredients with SARM1 inhibitory activity have been identified. Therefore, we here focused on dietary ingredients and found that carnosol, an antioxidant contained in rosemary, inhibits the NAD-cleavage activity of SARM1. Purified carnosol inhibited the enzymatic activity of SARM1 and suppressed neurite degeneration and cell death induced by the anti-cancer medicine vincristine (VCR). Carnosol also inhibited VCR-induced hyperalgesia symptoms, suppressed the loss of intra-epidermal nerve fibers in vivo, and reduced the blood fluid level of phosphorylated neurofilament-H caused by an axonal degeneration event. These results indicate that carnosol has a neuroprotective effect via SARM1 inhibition in addition to its previously known antioxidant effect via NF-E2-related factor 2 and thus suppresses neurotoxin-induced peripheral neuropathy.
含无菌α和Toll/白细胞介素受体基序蛋白1(SARM1)是一种烟酰胺腺嘌呤二核苷酸(NAD)水解酶,参与轴突变性和神经元细胞死亡。SARM1在引发外周神经病变、创伤性脑损伤和神经退行性疾病所基于的神经退行性过程中起关键作用。重要的是,敲低或敲除SARM1可防止变性;因此,SARM1作为一个有效的治疗靶点一直备受关注。近年来,已有报道开发了几种源自合成化合物的SARM1抑制剂;然而,尚未鉴定出具有SARM1抑制活性的膳食成分。因此,我们在此关注膳食成分,发现迷迭香中含有的抗氧化剂鼠尾草酸可抑制SARM1的NAD切割活性。纯化的鼠尾草酸抑制SARM1的酶活性,并抑制抗癌药物长春新碱(VCR)诱导的神经突变性和细胞死亡。鼠尾草酸还抑制VCR诱导的痛觉过敏症状,抑制体内表皮内神经纤维的丧失,并降低轴突变性事件引起的磷酸化神经丝-H的血液水平。这些结果表明,鼠尾草酸除了通过NF-E2相关因子2具有先前已知的抗氧化作用外,还通过抑制SARM1具有神经保护作用,从而抑制神经毒素诱导的外周神经病变。