# Boscisucrophage: A Natural SGLT1/2 Inhibitor From Boscia senegalensis for Managing Type 2 Diabetes

**Authors:** Bruno Eto, Amal Elrherabi, Fahd A. Nasr, Joe Miantezila Basilua, Ahlam Outman, Rosette Christelle Ndjip, Mohamed Bouhrim, Mohammed Al‐zharani, Ashraf Ahmed Qurtam, Brahim Ibet, Bernard Gressier, Jehan‐François Desjeux

PMC · DOI: 10.1002/fsn3.71621 · Food Science & Nutrition · 2026-03-08

## TL;DR

A natural extract from Boscia senegalensis, called Boscisucrophage, may help manage type 2 diabetes by reducing blood sugar and improving symptoms.

## Contribution

Boscisucrophage is proposed as a novel dual SGLT1/SGLT2 inhibitor for managing type 2 diabetes.

## Key findings

- BSP significantly reduced glycemia and HbA1c levels in T2DM patients.
- BSP increased urine glucose excretion and improved functional symptoms.
- No significant adverse effects on liver or kidney function were observed.

## Abstract

Boscia senegalensis
 (Pers.) Lam. Ex Poir. (Capparaceae) is an important local famine food plant in Africa and is widely exploited by healers in the Sahelian region for its seeds, which are used to reduce hyperglycemia. We studied the efficacy of the commercial dosage form of 
Boscia senegalensis
, namely Boscisucrophage (BSP), in type 2 diabetes (T2DM) patients with resistance to oral antihyperglycemic drugs. The clinical benefits of BSP were in a prospective, single‐center, open‐label, single‐arm interventional study involving 43 naïve patients and 289 diabetic patients resistant to oral antidiabetic drugs. All patients received capsules containing a fixed dose of 350 mg of BSP, taken three times daily for 12 weeks. Outcomes were monitored through venous blood glucose levels, glycosylated hemoglobin (HbA1c), urine glucose excretion (UGE), aspartate aminotransferase, alanine aminotransferase, creatinine levels, and clinical examination of functional symptoms. In the clinical study, BSP significantly reduced glycemia and HbA1c levels, increased urine glucose excretion (UGE), and alleviated the side effects and functional symptoms of T2DM. Our clinical findings provide preliminary evidence supporting the potential use of BSP to reduce glycemia and HbA1c in T2DM patients resistant to oral antihyperglycemic drugs, with no significant adverse effects observed in this study. These results highlight BSP's potential as a dual SGLT1/SGLT2 inhibitor, suggesting a novel mechanism of action. However, further validation through randomized controlled trials is necessary to confirm these findings.

Trial Registration: National Ethics Committee (N°679/PR/PM/MSP/SE/SG/DHATC/SGH/SRH/13)

Boscisucrophage (BSP) significantly reduced blood glucose and HbA1c, increased urine glucose excretion, and improved functional symptoms in T2DM patients resistant to oral antihyperglycemic drugs. BSP showed no adverse effects on liver or kidney function. These findings suggest BSP as a potential dual SGLT1/SGLT2 inhibitor, warranting further validation in randomized controlled trials.

## Linked entities

- **Diseases:** type 2 diabetes (MONDO:0005148), T2DM (MONDO:0005148)
- **Species:** Boscia senegalensis (taxon 1198336)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, SLC5A1 (solute carrier family 5 member 1) [NCBI Gene 6523] {aka D22S675, NAGT, SGLT-1, SGLT1}
- **Diseases:** obesity (MESH:D009765), nausea (MESH:D009325), fatigue (MESH:D005221), overweight (MESH:D050177), diarrhea (MESH:D003967), metabolic disorder (MESH:D008659), vomiting (MESH:D014839), headache (MESH:D006261), hepatic impairment (MESH:D008107), gastric ulcer (MESH:D013276), Hyperglycemia (MESH:D006943), impaired (MESH:D060825), Diabetes (MESH:D003920), abdominal pain (MESH:D015746), polyuria (MESH:D011141), dry mouth (MESH:D014987), T2DM (MESH:D003924), renal dysfunction (MESH:D007674), paresthesia (MESH:D010292), liver function abnormalities (MESH:D056486), constipation (MESH:D003248), type 1 diabetes (MESH:D003922), deaths (MESH:D003643), infections (MESH:D007239), hypoglycemia (MESH:D007003), cardiovascular compromise (MESH:D002318), gastrointestinal side effects (MESH:D064420), Weight loss (MESH:D015431), urinary and genital infections (MESH:D014552), dizziness (MESH:D004244), impotence (MESH:D007172), deficiency in insulin secretion (MESH:D007333)
- **Chemicals:** water (MESH:D014867), canagliflozin (MESH:D000068896), Metformin (MESH:D008687), Luseogliflozin (MESH:C549343), Empagliflozin (MESH:C570240), alkaloids (MESH:D000470), Blood glucose (MESH:D001786), N (MESH:D009584), triglycerides (MESH:D014280), polyphenols (MESH:D059808), Phloridzin (MESH:D010695), lipid (MESH:D008055), sterols (MESH:D013261), flavonoids (MESH:D005419), D-glucose (MESH:D005947), Creatinine (MESH:D003404), saponins (MESH:D012503), BS (-), Glimepiride (MESH:C057619), sodium (MESH:D012964), caffeine (MESH:D002110), amino acids (MESH:D000596), Glucocapparin (MESH:C000613398), Tofogliflozin (MESH:C575086), triterpenes (MESH:D014315), carbohydrate (MESH:D002241), dapagliflozin (MESH:C529054)
- **Species:** Lens culinaris (lentil, species) [taxon 3864], Eleusine coracana (coracan, species) [taxon 4511], Boscia senegalensis (species) [taxon 1198336], Panicum miliaceum (broomcorn millet, species) [taxon 4540], Raiamas senegalensis (Senegal minnow, species) [taxon 516811], Mus musculus (house mouse, species) [taxon 10090], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Homo sapiens (human, species) [taxon 9606]

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12967618/full.md

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Source: https://tomesphere.com/paper/PMC12967618