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Table 3 Pharmacological activities of patchouli on peptic ulcer

From: Pharmacological activities and mechanisms of action of Pogostemon cablin Benth: a review

Chemical name

Animals & pathological model

Efficient doses & administration route

Mechanisms

References

Pogostone

SD Rats; Indomethacin-induced gastric ulcer

10, 20 and 40 mg/kg, oral administration

SOD↑, GSH↑, CAT↑, PGE2↑, COX-1↑, COX-2↑, HSP-70↑, Bcl-2↑, MDA↓, Bax↓

[48, 49]

PAO

SD Rats; Ethanol-induced gastric ulcer

10, 20 and 40 mg/kg, oral administration

GSH↑, SOD↑, CAT↑, IL-10↑, MDA↓, caspase-3↓, Fas↓, Fasl ↓, TNF-α↓, IL-1β↓

[50]

β-PAE

SD Rats, Ethanol-induced gastric injury

10, 20 and 40 mg/kg, oral administration

SOD↑, GSH↑, CAT ↑

MDA↓, TNF-α↓, IL-1β↓, IL-6↓, Fas↓, FasL↓, caspase-3 ↓

[51]

PO

SD Rats; 2,4,6-trinitrobenzenesulfonic acid-induced IBD

270 mg/kg, rectal instillation

MPO↓

[56]

PA

BalB/C mice; dextran sulfate sodium-induced colitis

10, 20 and 40 mg/kg, oral administration

MPO↓, TNF-α↓, IFN-γ↓, IL-1β↓, IL-6↓, IL-4↓, IL-10↓, ZO-1, ZO-2↑, claudin-1↑, occludin↑, mucin-1↑, mucin-2↑, Bax↓, Bcl-2↑, RIP3↓, MLKL↓, IDO-1↓, TPH-1↓,

[57]

C57BL/6 mice; dextran sulphate sodium-induced colitis

6.25, 12.5 and 25 mg/kg, oral administration

CYP3A4↑, PXR ↑ NF-κB↓, IL-1β↓, IL-6↓, IL-10↓, TNF-α ↓

[48]

  1. Arrow up denotes activation; arrow down denotes suppression