Effect of the Antioxidant Supplement Pyrroloquinoline Quinone Disodium Salt (BioPQQ™) on Cognitive Functions

Author(s):  
Yuji Itoh ◽  
Kyoko Hine ◽  
Hiroshi Miura ◽  
Tatsuo Uetake ◽  
Masahiko Nakano ◽  
...  
2015 ◽  
Vol 61 (3) ◽  
pp. 241-246 ◽  
Author(s):  
Masahiko NAKANO ◽  
Ayako KAMIMURA ◽  
Fumiko WATANABE ◽  
Toshikazu KAMIYA ◽  
Daisuke WATANABE ◽  
...  

2021 ◽  
pp. 1-10
Author(s):  
Reham M. Abdel-Kader ◽  
Engy A Fadel ◽  
Reham M. Abdel-Kader

Background: Mitochondrial biogenesis has been recently implicated to play an important role in Alzheimer’s disease (AD). Recently it has been reported that brains of AD patients show reduced expression in major genes and proteins such as PGC-1α involved in mitochondrial biogenesis. This led to the idea that enhancing mitochondrial biogenesis in AD, might represent a plausible strategy for AD treatment. Pyrroloquinoline quinone (PQQ) has been recently implicated in enhancing cognitive functions during aging; however, its effect on mitochondrial biogenesis in neuroinflammatory AD mouse model was not previously examined. Objective: The aim of this project was to test the cognitive enhancement effect of PQQ in a neuroinflammatory mouse model mimicking AD, and whether PQQ is able to activate mitochondrial biogenesis in brains of our AD mouse model. Methods: Neuroinflammatory AD mouse model was developed by Lipopolysaccharide (250 g kg-1 body weight, i.p) injection for 7 days, followed by daily PQQ treatment (10 mg kg-1 body weight) on days 4-7. Cognitive functions were assessed using Y-Maze, Water-Maze and object recognition tests. Neurodegeneration was evaluated using H&E. Finally, mitochondrial proteins were measured using immunohistochemistry. Results: PQQ treatment improved spatial recognition and working memory. PQQ treated mice brains showed decreased levels of neurodegeneration. Moreover, their brains showed greater amounts of both PGC-1α and the mitochondrial-membrane-bound protein cytochrome-c, indicating enhancement of mitochondrial biogenesis. Conclusion: This study demonstrates the ability of PQQ to improve memory in neuroinflammatory AD model via enhancing mitochondrial biogenesis, which may represent an alternative mechanistic approach for treating AD.


Author(s):  
Kazuto Ikemoto ◽  
Shigeki Mori ◽  
Kazuo Mukai

Pyrroloquinoline quinone (PQQ) is a water-soluble quinone compound first identified as a cofactor of alcohol- and glucose-dehydrogenases (ADH and GDH) in bacteria. For example, in the process of ADH reaction, alcohol is oxidized to the corresponding aldehyde, and inversely PQQ is reduced to pyrroloquinoline quinol (PQQH2). PQQ and PQQH2molecules play an important role as a cofactor in ADH and GDH reactions. However, crystal structure analysis has not been performed for PQQ and PQQH2. In the present study, the synthesis of PQQH2powder crystals was performed under air, by utilizing vitamin C as a reducing agent. By reacting a trihydrate of disodium salt of PQQ (PQQNa2·3H2O) with excess vitamin C in H2O at 293 and 343 K, yellowish brown and black powder crystals of PQQH2having different properties were obtained in high yield, respectively. The former was PQQH2trihydrate (PQQH2·3H2O) and the latter was PQQH2anhydrate (PQQH2). Furthermore, sodium-free red PQQ powder crystal (a monohydrate of PQQ, PQQ·H2O) was prepared by the reaction of PQQNa2·3H2O with HCl in H2O. Single crystals of PQQH2and PQQ were prepared from Me2SO/CH3CN mixed solvent, and we have succeeded in the crystal structure analyses of PQQH2and PQQ for the first time.


2013 ◽  
Vol 67 (2) ◽  
pp. 189-197 ◽  
Author(s):  
Masahiko Nakano ◽  
Hiroshi Suzuki ◽  
Tadashi Imamura ◽  
Annette Lau ◽  
Barry Lynch

EFSA Journal ◽  
2017 ◽  
Vol 15 (11) ◽  
Author(s):  
◽  
Dominique Turck ◽  
Jean‐Louis Bresson ◽  
Barbara Burlingame ◽  
Tara Dean ◽  
...  

2014 ◽  
Vol 70 (1) ◽  
pp. 107-121 ◽  
Author(s):  
Masahiko Nakano ◽  
Hisaaki Takahashi ◽  
Seiko Koura ◽  
Catherine Chung ◽  
Shahrzad Tafazoli ◽  
...  

2015 ◽  
Vol 75 ◽  
pp. 146-150 ◽  
Author(s):  
Chunlai Liang ◽  
Xin Zhang ◽  
Wei Wang ◽  
Yan Song ◽  
Xudong Jia

2016 ◽  
Vol 39 ◽  
Author(s):  
Giosuè Baggio ◽  
Carmelo M. Vicario

AbstractWe agree with Christiansen & Chater (C&C) that language processing and acquisition are tightly constrained by the limits of sensory and memory systems. However, the human brain supports a range of cognitive functions that mitigate the effects of information processing bottlenecks. The language system is partly organised around these moderating factors, not just around restrictions on storage and computation.


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