# Global profiling of α-glucosidase inhibitors from Citri Reticulatae Pericarpium based on affinity ultrafiltration screening coupled with UPLC-ESI-Orbitrap-MS method

**Authors:** Hongping Wang, Qiong Yin, Zhaozhou Lin, Quantao Ma, Zhaohua Zhang, Jun Jia

PMC · DOI: 10.1371/journal.pone.0340990 · PLOS One · 2026-01-13

## TL;DR

This study identifies 84 compounds in Citri Reticulatae Pericarpium that inhibit α-glucosidase, a key enzyme in blood sugar regulation, suggesting potential anti-diabetic properties.

## Contribution

The first systematic identification of α-glucosidase inhibitors in Citri Reticulatae Pericarpium using advanced analytical methods.

## Key findings

- 84 active ingredients were identified as α-glucosidase inhibitors from Citri Reticulatae Pericarpium.
- Most of the inhibitors were multimethoxy flavonoids, which show potential anti-diabetic activity.
- Inhibiting α-glucosidase is likely a key mechanism for the herb's hypoglycemic effects.

## Abstract

As a medicinal and edible herb, Citri Reticulatae Pericarpium has multiple biological activities. The latest modern pharmacological researches have found that Citri Reticulatae Pericarpium has the effect of lowering blood sugar, and its extract can inhibit the activity of α-glucosidase. However, which component has inhibitory activity on α-glucosidase and the degree of inhibition are not clear. In order to solve this problem, this study used affinity ultrafiltration screening coupled with UPLC-ESI-Orbitrap-MS method to systematically screen α-glucosidase inhibitors from Citri Reticulatae Pericarpium for the first time. Through affinity ultrafiltration technology, the active components were selected, and through UPLC-ESI-Orbitrap-MS technology, their structures were identified. Finally, total 84 active ingredients were selected as α-glucosidase inhibitors, and most of them were multimethoxy flavonoids. Our results indicated that inhibiting α-glucosidase activity was probably one of the most important mechanisms for Citri Reticulatae Pericarpium exerting its hypoglycemic effect. In addition, our results first reported that multimethoxy flavonoids had the effects of hypoglycemic activity and potential anti-diabetes value.

## Linked entities

- **Diseases:** diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** SI (sucrase-isomaltase) [NCBI Gene 6476]
- **Diseases:** Digestive (MESH:D004828), chronic obstructive pulmonary disease (MESH:D029424), respiratory diseases (MESH:D012140), coronary heart disease (MESH:D003327), cardiovascular diseases (MESH:D002318), heart failure (MESH:D006333), bone-related disorders (MESH:D001847), Alzheimer's disease (MESH:D000544), nausea (MESH:D009325), diabetes (MESH:D003920), inflammation (MESH:D007249), irritable bowel syndrome (MESH:D043183), Parkinson's disease (MESH:D010300), bronchiectasis (MESH:D001987), digestive system diseases (MESH:D004066), hypoglycemic (MESH:C000721848), abdominal distension (MESH:D000007), vomiting (MESH:D014839), stroke (MESH:D020521), chronic gastritis (MESH:D005756), obesity (MESH:D009765), angina pectoris (MESH:D000787), asthma (MESH:D001249), gastric cancer (MESH:D013274), cancer (MESH:D009369)
- **Chemicals:** carbohydrate (MESH:D002241), THR- (MESH:D013912), hesperidin (MESH:D006569), TYR- (MESH:D014443), vicenin-2 (MESH:C530449), ASP- (MESH:D001224), 5-Demethylnobiletin (MESH:C000604601), CHO (MESH:C034482), naringenin (MESH:C005273), ARG (MESH:D001120), Tween 20 (MESH:D011136), Phosphate (MESH:D010710), diosmetin (MESH:C039602), DMSO (MESH:D004121), H (MESH:D006859), nobiletin (MESH:C008661), ASN (MESH:D001216), C2 (MESH:C023714), ammonium acetate (MESH:C018824), HIS- (MESH:D006639), water (MESH:D014867), 4',5,6,7-tetramethoxyflavone (MESH:C072809), flavonoids (MESH:D005419), C1 (MESH:C400149), PBS (MESH:D007854), blood sugar (MESH:D001786), miglitol (MESH:C045621), LEU (MESH:D007930), sugar (MESH:D000073893), formic acid (MESH:C030544), Glc (MESH:D005947), methanol (MESH:D000432), sinensetin (MESH:C059295), 5-hydroxy-3,7,3',4'-tetramethoxyflavone (MESH:C000622038), neohesperidin (MESH:C546526), GLU- (MESH:D018698), rhoifolin (MESH:C089378), naringenin-7-O-glucoside (MESH:C529068), voglibose (MESH:C102817), C60 (MESH:C069837), VAL (MESH:D014633), N (MESH:D009584), Kaempferol-3-O-rutinoside (MESH:C492687), S (MESH:D013455), tangeretin (MESH:C059006), naringin (MESH:C005274), GLN (MESH:D005973), Acarbose (MESH:D020909), Rha (MESH:D012210), 3A4A. (-), Isoquercitroside (MESH:C016527), acetonitrile (MESH:C032159), eriocitrin (MESH:C114706), p-Nitrophenyl-alpha-D-glucopyranoside (MESH:C019502), Sodium carbonate (MESH:C005686), hesperetin (MESH:C013015)
- **Species:** Citrus reticulata (mandarin orange, species) [taxon 85571], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Citrus (genus) [taxon 2706]

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12798990/full.md

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Source: https://tomesphere.com/paper/PMC12798990