| Literature DB >> 27754463 |
Derong Lin1, Mengshi Xiao2, Jingjing Zhao3, Zhuohao Li4, Baoshan Xing5, Xindan Li6, Maozhu Kong7, Liangyu Li8, Qing Zhang9, Yaowen Liu10, Hong Chen11, Wen Qin12, Hejun Wu13, Saiyan Chen14.
Abstract
In this paper, the biosynthesis process of phenolic compounds in plants is summarized, which include the shikimate, pentose phosphate and phenylpropanoid pathways. Plant phenolic compounds can act as antioxidants, structural polymers (lignin), attractants (flavonoids and carotenoids), UV screens (flavonoids), signal compounds (salicylic acid, flavonoids) and defense response chemicals (tannins, phytoalexins). From a human physiological standpoint, phenolic compounds are vital in defense responses, such as anti-aging, anti-inflammatory, antioxidant and anti-proliferative activities. Therefore, it is beneficial to eat such plant foods that have a high antioxidant compound content, which will cut down the incidence of certain chronic diseases, for instance diabetes, cancers and cardiovascular diseases, through the management of oxidative stress. Furthermore, berries and other fruits with low-amylase and high-glucosidase inhibitory activities could be thought of as candidate food items in the control of the early stages of hyperglycemia associated with type 2 diabetes.Entities:
Keywords: biosynthesis; complication; function; phenolic compounds; type 2 diabetes
Mesh:
Substances:
Year: 2016 PMID: 27754463 PMCID: PMC6274266 DOI: 10.3390/molecules21101374
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411
Figure 1Common phenolic compounds in plants comprise an aromatic ring, bear one or more hydroxyl substituents and range from simple phenolic molecules to highly polymerized compounds (modified from Velderrain-Rodríguez et al., 2014) [2].
Figure 2Biosynthesis of phenol compounds in the pentose phosphate, shikimate and phenylpropanoid pathways in plants (modified from Vattem et al., 2005, and Lin et al., 2010) [3,4].
Figure 3Reactive oxygen (ROS) and nitrogen (RNS) species are highly reactive oxidized molecules, including superoxide, peroxide, singlet oxygen, hydroxyl radical, NO and OONO, that are constantly produced under normal cellular conditions, such as during homeostasis and impaired functions, which could lead to cellular damage, like ageing, disease and cell death (modified from Shetty et al., 2004.) [20].
Fasted body weight, body weight gain, tissue weight, ratio of tissue-to-body weight and hemoglobin A1 of rats after the experiment for four weeks a [23].
| Wt, Wt Gain and Ratio | Normal | Control | Crude Extract of | Crude Extract of |
|---|---|---|---|---|
| Final body wt (g) | 337.8 ± 17.7 | 238.2 ± 22.6 c | 239.5 ± 19.4 c | 244.7 ± 12.6 c |
| Body wt gain (g) | 142.4 ± 14.5 | 55.2 ± 16.2 c | 56.4 ± 14.2 c | 60.1 ± 7.7 c |
| Liver wt (g) | 10.65 ± 0.73 | 8.96 ± 0.72 c | 8.30 ± 0.64 c | 8.02 ± 0.83 c |
| Kidney wt (g) | 2.462 ± 0.189 | 2.208 ± 0.263 | 1.895 ± 0.310 c | 1.846 ± 0.359 c |
| Pancreas wt (g) | 0.946 ± 0.180 | 0.597 ± 0.076 c | 0.632 ± 0.151 c | 0.664 ± 0.081 c |
| Tissue-to-body wt ratio b Liver (g/100 g) | 3.162 ± 0.294 | 3.771 ± 0.216 | 3.485 ± 0.378 | 3.288 ± 0.434 |
| Kidney (g/100 g) | 0.730 ± 0.071 | 0.930 ± 0.111 c | 0.789 ± 0.093 | 0.751 ± 0.115 |
| Pancreas (g/100 g) | 0.279 ± 0.042 | 0.252 ± 0.032 | 0.266 ± 0.067 | 0.271 ± 0.032 |
| Hemoglobin A1 (%) | 2.16 ± 0.18 | 4.27 0.60 c | 3.29 ± 0.84 c | 2.65 ± 0.36 d |
a Rats were fasted for 20 h after the experimental period of 4 weeks. Data represent the mean ± SD of five rats. b Tissue weight per 100 g of body weight. Significant difference is indicated from the normal c and control d groups at p < 0.05.
Figure 4OH radical scavenging ability of gallic and protocatechuic acids.
Figure 5Fe2+ chelating ability of gallic and protocatechuic acids.
Enzyme inhibitors from plant origins and their corresponding inhibition of enzymes in starch digestion.
| Plant Origin | Enzyme Inhibitor | Enzyme Targets | References |
|---|---|---|---|
| Pakhanbhed | (−)-3- | Pancreatic α-amylase, maltase | Bhandari et al., 2008 [ |
| Persimmon | Proanthocyanidin ((−)-epigallocatechin, (−)-epigallocatechin-3- | Pancreatic α-amylase | Kawakami et al., 2010 [ |
| Finger millet | Naringenin, kaempferol, luteolin glycoside, apigenin, daidzein, caffeic acid, ferulic acid, syringic acid | Pancreatic α-amylase, α-glucosidase | Shobana et al., 2009 [ |
| Raspberries | Ellagic acid, catechin, pelargonidin-3-rutinoside, cyanidin-diglucoside | α-Glucosidase | Zhang et al., 2011 [ |
| Black myrobalan | Chebulanin, chebulagic acid, chebulinic acid | Maltase | Gao et al., 2007 [ |
| Black/bitter cumin ( | Caffeic acid, ellagic acid, ferulic acid, quercetin, kaempferol | Maltase, sucrase, salivary α-amylase | Ani and Akhilender Naidu., [ |