Yamashita Haruhiro, Hoenerhoff Mark J, Shockley Keith R, Peddada Shyamal D, Gerrish Kevin E, Sutton Deloris, Cummings Connie A, Wang Yu, Julie Foley F, Behl Mamta, Waidyanatha Suramya, Sills Robert C, Pandiri Arun R
1 National Toxicology Program, National Institute of Environmental Health Sciences (NIEHS), Research Triangle Park, North Carolina, USA.
2 Taisho Pharmaceutical Co. Ltd., Saitama, Japan.
Toxicol Pathol. 2018 Jul;46(5):564-573. doi: 10.1177/0192623318778796. Epub 2018 May 27.
There was a significant increase in the incidence of retinal degeneration in F344/N rats chronically exposed to Kava kava extract (KKE) in National Toxicology Program (NTP) bioassay. A retrospective evaluation of these rat retinas indicated a similar spatial and morphological alteration as seen in light-induced retinal degeneration in albino rats. Therefore, it was hypothesized that KKE has a potential to exacerbate the light-induced retinal degeneration. To investigate the early mechanism of retinal degeneration, we conducted a 90-day F344/N rat KKE gavage study at doses of 0 and 1.0 g/kg (dose which induced retinal degeneration in the 2-year NTP rat KKE bioassay). The morphological evaluation indicated reduced number of phagosomes in the retinal pigment epithelium (RPE) of the superior retina. Transcriptomic alterations related to retinal epithelial homeostasis and melatoninergic signaling were observed in microarray analysis. Phagocytosis of photoreceptor outer segment by the underlying RPE is essential to maintain the homeostasis of the photoreceptor layer and is regulated by melatonin signaling. Therefore, reduced photoreceptor outer segment disc shedding and subsequent lower number of phagosomes in the RPE and alterations in the melatonin pathway may have contributed to the increased incidences of retinal degeneration observed in F344/N rats in the 2-year KKE bioassay.
在国家毒理学计划(NTP)生物测定中,长期暴露于卡瓦提取物(KKE)的F344/N大鼠视网膜变性的发生率显著增加。对这些大鼠视网膜的回顾性评估表明,其空间和形态改变与白化大鼠光诱导性视网膜变性中所见相似。因此,推测KKE有可能加剧光诱导性视网膜变性。为了研究视网膜变性的早期机制,我们进行了一项为期90天的F344/N大鼠KKE灌胃研究,剂量为0和1.0 g/kg(该剂量在为期两年的NTP大鼠KKE生物测定中诱导了视网膜变性)。形态学评估表明,视网膜上半部分视网膜色素上皮(RPE)中的吞噬体数量减少。在微阵列分析中观察到与视网膜上皮稳态和褪黑素能信号相关的转录组改变。下层RPE对光感受器外段的吞噬作用对于维持光感受器层的稳态至关重要,并且受褪黑素信号调节。因此,光感受器外段盘状物脱落减少以及随后RPE中吞噬体数量降低以及褪黑素途径的改变可能导致了在为期两年的KKE生物测定中F344/N大鼠视网膜变性发生率增加。