Hatakawa Yusuke
Department of Bio-analytical Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University.
Nihon Yakurigaku Zasshi. 2024;159(6):396-401. doi: 10.1254/fpj.24075.
We have reported on two Catalytides (Catalytic peptides), JAL-TA9 (YKGSGFRMI) and ANA-TA9 (SKGQAYRMI). Both peptides belong to the Tob/BTG family proteins and cleave Aβ42. Although Catalytides must be delivered to the brain parenchyma to treat Alzheimer's disease, the blood-brain barrier (BBB) limits their entry into the brain from the systemic circulation. Thus, we evaluated the direct route of ANA-TA9 from the nasal cavity to the brain to bypass the BBB. In this study, we present our findings on JAL-TA9. Animal studies using rats and mice clarified that the plasma clearance of JAL-TA9 was more rapid than its in vitro degradation in plasma, whole blood, and cerebrospinal fluid (CSF). After nasal administration of JAL-TA9, brain concentrations were significantly higher than after intraperitoneal administration, despite much lower plasma concentration. This observation strongly suggests direct delivery of JAL-TA9 to the brain from the nasal cavity. Similar findings were observed for its transport to CSF after nasal and intravenous administration. The concentration of JAL-TA9 in the olfactory bulb peaked at 5 min, while those in the frontal brain peaked at 30 min and in the occipital brain at 60 min. In conclusion, JAL-TA9 was efficiently delivered to the brain by nasal application compared to other routes.
我们曾报道过两种催化肽(Catalytides),即JAL-TA9(YKGSGFRMI)和ANA-TA9(SKGQAYRMI)。这两种肽都属于Tob/BTG家族蛋白,且能切割Aβ42。尽管催化肽必须递送至脑实质才能治疗阿尔茨海默病,但血脑屏障(BBB)限制了它们从体循环进入大脑。因此,我们评估了ANA-TA9从鼻腔至大脑的直接途径,以绕过血脑屏障。在本研究中,我们展示了关于JAL-TA9的研究结果。使用大鼠和小鼠进行的动物研究表明,JAL-TA9在血浆中的清除速度比其在血浆、全血和脑脊液(CSF)中的体外降解速度更快。鼻腔给予JAL-TA9后,尽管血浆浓度低得多,但脑内浓度显著高于腹腔注射后。这一观察结果强烈提示JAL-TA9可从鼻腔直接递送至大脑。鼻腔和静脉给药后,其向脑脊液的转运也观察到类似结果。JAL-TA9在嗅球中的浓度在5分钟时达到峰值,而在前脑在30分钟时达到峰值,在枕叶脑在60分钟时达到峰值。总之,与其他途径相比,鼻腔给药能有效地将JAL-TA9递送至大脑。