Sains Malaysiana
53(4)(2024): 795-805
http://doi.org/10.17576/jsm-2024-5304-06
Novel Blood
Pressure-Lowering Effect of Spathulenol in Rats
(Kesan
Penurunan Tekanan Darah Novel Spathulenol pada Tikus)
RASLAN
AIN-FATIN1, YEE YONG MEI1, HOE SEE ZIAU2, ONG
HOOI TIN1 & LAM SAU KUEN1,*
1Department of Pre-clinical Science, M.
Kandiah Faculty of Medicine and Health Sciences, Universiti Tunku Abdul Rahman,
Bandar Sungai Long, 43000 Kajang, Selangor, Malaysia
2 Department of Physiology, Faculty
of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
Received: 14 September 2023/Accepted: 27 February 2024
Abstract
In recent years, natural compounds from plant sources are sought after as alternative anti-hypertensive treatments. Spathulenol (Spa), a terpenoid plant metabolite obtained mainly from the Origanum species has shown anecdotal evidence of blood pressure (BP)-lowering properties probably through the effects on vasoreactivity. This study aimed to investigate the BP-lowering activities of Spa in vivo as well as to ascertain the mechanisms of action in vitro. Male Sprague-Dawley (SD) rats (n=16) and spontaneously hypertensive rats (SHR) (n=16) with their normotensive Wistar-Kyoto (WKY) rats (n=16) as controls were subjected to anaesthesia and administered intravenous boluses of Spa at 0.0, 0.045, 0.90, 0.18, 0.36, and 0.7 mg/kg or positive control losartan at 0.0, 0.6, 1.2, 1.8, 2.4 and 3.0 mg/kg. The BP and heart rate (HR) of the rats were recorded by a computerised physiographical system (Power Lab) through carotid arterial cannulation that was connected to a pressure transducer. The data were analysed by using the Lab Chart 6 software. Spathulenol was also tested for angiotensin-converting enzyme (ACE) inhibitory activity by using the ACE1 inhibitor screening kit (PromoKine). Spathulenol was able to decrease the BP of rats in a dose-dependent manner with the BP-lowering effect being significantly (p < 0.05) higher in the SHRs than in the WKY controls. Furthermore, Spa was able to inhibit the ACE activity suggesting the possibility that this could be one of the mechanisms underlying the observed BP-lowering effect.
Keywords: Angiotensin-converting
enzyme inhibition; blood pressure; Spathulenol; spontaneously hypertensive
rats; Wistar-Kyoto rats
Abstrak
Dalam beberapa tahun kebelakangan ini, sebatian semula jadi daripada sumber tumbuhan telah didekati sebagai salah satu bentuk untuk rawatan anti-hipertensif. Spathulenol (Spa), metabolit tumbuhan terpenoid yang diperoleh terutamanya daripada spesies Origanum telah menunjukkan bukti anekdot tentang sifat menurunkan tekanan darah mungkin melalui kesan ke atas vasoreaktiviti. Oleh itu, penyelidikan ini dilakukan untuk mengkaji aktiviti penurunan tekanan darah Spa secara in vivo serta memastikan mekanisme tindakan secara in vitro. Tikus jantan Sprague-Dawley (SD) (n=16), tikus hipertensi spontan (SHR) (n=16) dan tikus Wistar-Kyoto (WKY) (n=16) sebagai kawalan normotensif telah diletakkan di bawah anestesia dan diberikan bolus intravena Spa sebanyak 0.0, 0.045, 0.90, 0.18, 0.36 dan 0.7 mg/kg atau kontrol positif losartan sebanyak 0.0, 0.6, 1.2, 1.8, 2.4 dan 3.0 mg/kg. Tekanan darah dan kadar denyutan jantung tikus direkodkan oleh sistem fisiografi berkomputer (PowerLab) melalui kanulasi arteri karotid yang disambungkan kepada transduser tekanan. Data dianalisis menggunakan perisian LabChart 6. Spathulenol juga telah diuji untuk aktiviti perencatan enzim penukar angiotensin (ACE) menggunakan kit pemeriksaan perencat ACE1 (PromoKine). Spathulenol didapati dapat mengurangkan tekanan darah tikus dalam cara yang bergantung kepada dos dengan kesan penurunan tekanan darah secara signifikan (p < 0.05) lebih tinggi dalam SHR berbanding kawalan WKY. Tambahan pula, Spa dapat merencat aktiviti ACE yang menunjukkan kemungkinan bahawa ini boleh menjadi salah satu mekanisme yang mendasari kesan penurunan tekanan darah yang diperhatikan.
Kata kunci: Perencatan enzim
penukar angiotensin; Spathulenol; tekanan darah; tikus hipertensi spontan;
tikus Wistar-Kyoto
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*Corresponding author; email:
lamsk@utar.edu.my
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