Table 2.
Sr. No. | Objective | Experiment Model | Produced effects | Ref. |
---|---|---|---|---|
1 | Learning and memory function | Rats | Significantly improved learning ability and prevent neuron-degeneration caused by oxidative stress | (Takatsu et al., 2009; Ohwada et al., 2008) |
2 | Neuropsycho-logical status based on RBANS | Human | People whose RBANS scores are lower may see a more pronounced improvement after taking the PQQ•Na2-supplements | (Tamakoshi et al., 2023; Shiojima et al., 2022; Itoh et al., 2016) |
3 | Cognitive functions | Human | Significant improvement in task performance | Itoh et al. (2016) |
4 | Impacts on anxiety, fatigue, and sleeping | Human | A marked improvement in sleepiness upon awakening, the beginning of sleep, and the maintenance of sleep length | Nakano et al. (2012) |
5 | The impact on dry skin hydration levels, elasticity, and transepidermal water loss (TEWL) | Mice and Human | Benefits impaired skin barrier function as well as dry-skinned human female individuals and in mice model | Nakano et al. (2015a) |
6 | Impact on cholesterol and serum TGs levels | Human | PQQ reduce LDL-cholesterol levels | Nakano et al. (2015b) |
7 | Impacts on development, fertility, and markers of collagen expression and maturation | Balb/c mice | By modulating mRNA levels for Type I procollagen α1-chains, PQQ supplementation might improve growth, reproductive success, and possibly regulate indicators of the synthesis and maturation of the extracellular matrix (ECM) in neonates | Steinberg et al. (2003) |
8 | Nutritional essentiality of PQQ | Rats and mice | Animals fed with PQQ meals showed consistent signs of increased growth. A decrease in tendon benzylamine oxidase and an increase in cutaneous collagen solubility were seen in subjects deficient in PQQ | Rucker et al. (1989) |
9 | Effects on growth performance and small intestine characteristics | Weaned pigs | Reduced levels of cytokines (IL-1β, IL-2), and interferon-γ, along with improved activity of antioxidant enzymes (SOD, GSH-Px, CAT, and MDA) in the small intestine mucosa. The jejunum also showed an increase in the expression of occludin and zonula occluden protein-1 (ZO-1). Weaned piglets' growth performance and intestinal health were both significantly enhanced |
(Jiang et al., 2020; Yin et al., 2019) |
10 | Challenged intestinal morphology, oxidative stress, and inflammatory responses to lipopolysaccharide | Broiler chickens | Incorporating PQQ•Na2 into the diet reduce IL-1β and IL-10 levels at transcriptional level in the duodenum mucosa and enhanced GSH-Px activity in serum and T-SOD and CAT activities in liver. In addition, it reduces the effects of LPS on the duodenal villus height to bulb depth ratio in broilers. |
(Jiang et al., 2020; Zheng et al., 2020) |