Title:Effects of Standardized Aqueous Ethanolic Extract of Leaves of Ficus
Deltoidea var. Trengganuensis on Blood Pressure in Spontaneously
Hypertensive Rats
Volume: 14
Issue: 5
Author(s): Zurain Radjeni, Mardiana Abdul Aziz, Norasikin Ab Azis, Mohd Saleh Ahmad Kamal and Harbindar Jeet Singh*
Affiliation:
- Faculty of Medicine, Universiti Teknologi MARA, Cawangan Selangor, Sungai Buloh Campus, Selangor, Malaysia
- Institute For Medical Molecular
Biotechnology (IMMB), Faculty of Medicine, Universiti Teknologi MARA, Cawangan Selangor, Sungai Buloh
Campus, Selangor, Malaysia
- Institute for Pathology, Laboratory and Forensic Medicine (I-PPerFORM), Universiti
Teknologi MARA, Cawangan Selangor, Sungai Buloh Campus, Selangor, Malaysia
Keywords:
Ficus deltoidea var. trengganuensis, RAAS, eNOS, ET-1, blood pressure, spontaneously hypertensive rats.
Abstract:
Background: Laboratory evidence pertaining to the antihypertensive activity of a number
of Ficus deltoidea (FD) varieties remains undetermined, although extracts of some of these varieties
have been shown to have angiotensin-converting enzyme (ACE) inhibitory activity in vitro.
Objective: This study, therefore, evaluated the effect of a standardized aqueous-ethanolic extract of
leaves of Ficus deltoidea var. trengganuensis (FDT) on blood pressure in spontaneously hypertensive
rats (SHR).
Methods: SHR were given either 800, 1000 or 1200 mg kg-1 body weight of standardized aqueousethanolic
extract of FDT or 10 mg kg-1 body weight of losartan or 0.5 ml of distilled water daily for
four weeks.
Results: SBP decreased significantly in FDT- and losartan-treated rats (p < 0.05). Components of
RAAS and other serum and urinary parameters were not different between the groups except for
endothelin-1, which was significantly lower than that in the controls. Urinary calcium excretion was
significantly higher in FDT-treated rats (p < 0.05).
Conclusion: It seems that daily oral administration of FDT significantly lowers blood pressure in
SHR through mechanisms that do not involve RAAS but may involve the endothelium or other yetto-
be-determined mechanisms.