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Effects of Salvia sclarea on chronic immobilization stress induced endothelial dysfunction in rats
BMC Complementary and Alternative Medicine volume 14, Article number: 396 (2014)
Although Salvia sclarea (clary sage) is widely used in aromatherapy and has antioxidant and antimicrobial properties, its mechanisms of action remain poorly understood. We therefore assessed whether clary sage is effective in treating endothelial dysfunction induced by chronic immobilization stress in rats.
Rats were intraperitoneally injected with almond oil, clary sage oil (5%, 10% or 20%), or nifedipine once daily, followed by immobilization stress (2 h/day) for 14 days. Systolic blood pressure (SBP) and heart rate (HR) were measured, as were serum concentrations of corticosterone (CORT); a biomarker of chronic stress, malondialdehyde (MDA); a biomarker of oxidative stress. Nitric oxide production was assessed by nitrite assays, and eNOS level, a biomarker of endothelial dysfunction, was measured by western blotting. Endothelial dysfunction was also assayed by measuring the effect of clary sage on the contraction of rat aortae.
Treatment with 5% (p = 0.029), 10% (p = 0.008), and 20% (p = 0.008) clary sage significantly reduced SBP and treatment with 20% clary sage significantly reduced HR (p = 0.039) compared with the chronic immobilization stress group. Clary sage decreased CORT serum concentration (10%, p = 0.026; 20%, p = 0.012) and MDA (10%, p = 0.007; 20%, p = 0.027), findings similar to those observed with nifedipine. In addition, 20% clary sage significantly increased nitric oxide production (p <0.001) and eNOS expression level (p <0.001) and relaxed aortic rings in rats subjected to chronic immobilization stress.
Clary sage treatment of rats subjected to immobilization stress contributed to their recovery from endothelial dysfunction by increasing NO production and eNOS level as well as by decreasing oxidative stress. Appropriate concentration of clary sage may result in recovery from endothelial dysfunction. These findings indicate that clary sage oil may be effective in the prevention and treatment of stress-induced cardiovascular diseases.
Endothelial dysfunction is characterized by reduced vasodilation, both generally and in response to specific stimuli, as well as a proinflammatory and prothrombic state . Endothelial dysfunction has been implicated in the pathogenesis of several cardiovascular diseases, including hypertension, atherosclerosis, coronary artery disease, and chronic heart failure. Chronic immobilization and vascular oxidative stress lead to endothelial dysfunction and systolic hypertension, activating the angiotensin II and AT1 receptor signaling pathway . Responses to chronic stress include increased production of corticotropin-releasing hormone and increased central sympathetic activity, inducing cardiovascular reactivity including blood pressure and heart rate . Furthermore, chronic immobilization stress induces working memory impairment, anxiety and depressive-like behavior . Oxidative stress also causes endothelial dysfunction by impairing endothelium-dependent relaxation and by inducing intracellular calcium overload and DNA fragmentation in hypertensive models .
Endothelial dysfunction in hypertensive patients has also been associated with decreased production of nitric oxide (NO), a key vasodilator released by the endothelium. NO has been associated with various endothelial functions, including the regulation of vascular tone, platelet aggregation, and vascular smooth muscle cell proliferation . Therefore, endothelial dysfunction may result from the reduced activity of endothelial NO synthase and the resulting decreased bioavailability of NO .
Salvia sclarea (Clary sage) is an important aromatic plant of the mint family that has various pharmacological properties, including antioxidant and antimicrobial activities . Inhalation of clary sage has been shown to induce relaxation in patients with urinary incontinence by reducing systolic blood pressure . Blended essential oils containing clary sage, lavender and marjoram have been found to relieve pain in women with dysmenorrhea . In rats, clary sage has anti-depressant activity through modulation of the dopaminergic pathway . Despite its widespread use in aromatherapy and its therapeutic activities, little is known about the mechanisms of action of clary sage. We therefore assessed whether clary sage is effective in the treatment of rats with endothelial dysfunction induced by chronic immobilization stress.
Rat model of immobilization stress
Male Sprague–Dawley rats, aged 8 weeks and weighing 200–250 g (Samtaco INC., Osan, Korea), were acclimatized to standard laboratory conditions for 3–5 days. All experimental procedures were conducted in accordance with guidelines relevant to the care of experimental animals, as approved by the Animal Research Committee of Korea University (approval no. KUIACUC-2012-181), informed by the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85–23; revised 1996). Rats were randomized into five groups of seven to nine each and intraperitoneally injected with 0.1 ml/100 g body weight almond oil, clary sage oil (5%, 10%, or 20%, vol/vol), or nifedipine (10 mg/kg) once daily prior to the induction of immobilization stress by restraints. Rats were immobilized for 2 hours per day for 14 days using an adjustable restraining cage .
Clary sage oil was supplied by Aromarant Co. Ltd. (Rottingen, Germany) and diluted in almond oil. Nifedipine was purchased from Sigma-Aldrich (Steinheim, Germany), and dissolved in dimethyl sulfoxide.
Measurement of systolic blood pressure (SBP) and heart rate (HR)
The SBP and pulse signal level (heart rate) were measured one day before the first stress day and one day after the last stress day using a tail cuff and pulse transducer (ADInstruments, Sydney, Australia). Five measurements were taken at each time point and the mean systolic blood pressure calculated.
Blood sampling and serum corticosterone (CORT) assay
Blood samples were obtained the day after completion of stress treatment by cardiac puncture from rats anesthetized with isoflurane (Hana Pharm. Co., Ltd., Seoul, Korea). Samples were centrifuged for 15 min at 13,000 × g within 30 min of collection and stored at −80°C. CORT was assayed in serum using an ELISA kit (Assay Designs Inc. Ann Arbor, MI) according to the manufacturer’s instructions.
Malondialdehyde (MDA) and nitrite assays
Serum MDA concentration was measured spectrophotometrically at 532 nm as thiobarbituric acid reactive substances using a colorimetric/fluorometric assay kit according to the manufacturer’s instructions (Biovision, CA, USA). Serum nitrite concentration was measured by the Griess reaction. Briefly, 100 μl of Griess reagent (1% sulfanilamide, 0.1% naphthylethylenediamide in 5% phosphoric acid) was mixed with 50 μl of serum and incubated for 10 minutes at room temperature, and the optical density at 540 nm was determined using a microplate reader (BMG Labtech, Ortenberg, Germany).
Western blot analysis
Rat aorta homogenates were separated on 10% sodium dodecyl sulfate (SDS)-polyacrylamide gels. The proteins were electrophoretically transferred onto nitrocellulose membranes and blocked for 30 min at room temperature. Membranes were incubated overnight at 4°C with primary antibodies to eNOS and glyceraldehyde-3-phophate dehydrogenase (GAPDH) and then with horseradish peroxidase-conjugated secondary antibody for 1 h at room temperature. The signal was visualized by enhanced chemiluminescence (ECL) reagents according to the manufacturer’s protocol.
Preparation of isolated rat aortic rings
Isolated rat thoracic aortae were dissected to remove connective and fatty tissue and cut into rings about 4 to 5 mm in length. Rings were mounted in organ baths containing Krebs- Henseleit solution (118.3 mM NaCl, 4.78 mM KCl, 25 mM NaHCO3, 1.22 mM KH2PO4, 11.1 mM glucose, 2.5 mM CaCl2, and 1.2 mM MgCl2). The baths were maintained at 37°C and aerated with 95% O2 and 5% CO2 throughout the experiment. Resting tension (0.7-0.9 g) was applied for 1 h.
Data were expressed as mean ± standard error of the mean (SEM). Differences among treatment groups were evaluated by one-way ANOVA, followed by LSD post hoc test. A P value <0.05 was considered statistically significant.
Effects of clary sage on SBP and HR in chronic immobilization stress induced rat
As expected, SBP was significantly higher in rats immobilized 2 hours per day for 14 days compared with control rats (P <0.001) (data not shown). SBP was significantly decreased by treatment with 5% (132.02 ± 16.59 mmHg, P = 0.029), 10% (127.97 ± 22.70 mmHg, P = 0.008) and 20% (127.09 ± 12.18 mmHg, P = 0.008) clary sage compared with the stress group (152.82 ± 23.08 mmHg) after completion of 2-week immobilization (Figure 1A). Furthermore, 20% clary sage effectively reduced HR (404.54 ± 28.22 bpm, P = 0.039) compared with the stress group (450.85 ± 61.04 bpm) (Figure 1B). Nifedipine significantly decreased SBP (117.60 ± 15.71 mmHg, P <0.001) and HR (403.01 ± 50.61 mmHg, P = 0.028).
Effect of clary sage on CORT in chronic immobilization stress induced rats
Compared with chronic immobilization stress induced rats (72.82 ± 36.81 ng/mL), treatment with 10% (32.27 ± 28.45 ng/mL, P = 0.026) and 20% (24.83 ± 28.27 ng/mL, P = 0.012) clary sage significantly reduced serum CORT concentration. Similarly, nifedipine significantly reduced serum CORT concentration (21.86 ± 23.15 ng/mL, P = 0.008) (Figure 2).
Effect of clary sage on MDA in chronic immobilization stress induced rats
To investigate whether clary sage was associated with oxidative stress in chronic immobilization, we measured serum concentrations of MDA, a biomarker of oxidative stress. Clary sage decreased the serum level of MDA compared with immobilization stress group (105.27 ± 12.45 nM/mL) and this reduction was significant in 10% (73.89 ± 21.07 nM/mL, P = 0.007) and 20% (78.00 ± 13.51 nM/mL, P = 0.027) clary sage groups. Nifedipine showed a significant decrease compared with chronic immobilization stress group (80.87 ± 19.56 nM/mL, P = 0.037) (Figure 3).
Effect of clary sage on nitrite, eNOS and contraction of aortic rings in chronic immobilization stress induced rats
To demonstrate endothelial dysfunction, we focused on 20% clary sage which was the most efficient concentration in this study. Serum nitrite concentration, a biomarker of endothelial dysfunction, was significantly higher in immobilized rats administered 20% clary sage (47.88 ± 15.97 μ M, P <0.001) than in stressed rats (25.76 ± 8.37 μ M) (Figure 4A). Furthermore, 20% clary sage significantly increased eNOS expression levels 1.79-fold (P <0.001) in rats subjected to chronic immobilization stress (Figure 4B). Aortic rings obtained from rats treated with clary sage showed a greater relaxation tendency in response to ACh than vehicle treated rats (Figure 4C).
Exposure to chronic stress contributes to the development of hypertension and immobilization stress has been found to increase plasma concentrations of adrenocorticotropic hormone, corticosterone, norepinephrine and epinephrine, resulting in increased blood pressure and heart rate [11, 12]. This study was designed to investigate the protective effects of clary sage against chronic immobilization stress. We found that clary sage significantly reduced SBP and HR in rats subjected to immobilization stress. Furthermore, clary sage significantly decreased plasma CORT concentrations. The activities of clary sage were similar to those of the calcium channel blocker nifedipine, which is used to treat high blood pressure  and has been found to improve endothelial function by reducing oxidative stress and suppressing endothelial progenitor cell apoptosis .
Oxidative stress is increased in chronic stress conditions, including psychological stress in humans and restraint stress in animals . Excessive production of ROS has been reported to causes hypertension and scavenging of ROS has been shown to reduce blood pressure . Chronic immobilization stress by restraint has been found to alter the prooxidant-antioxidant balance, leading to the development of various pathological states such as mitochondrial dysfunction, disruption of energy pathways, neuronal damage, impaired neurogenesis and induction of signaling events in apoptotic cell death [4, 15]. Interestingly, we found that 20% clary sage decreased oxidative stress and increased NO production and eNOS expression in chronic immobilization induced rats.
Enhanced ROS production and destruction of the antioxidant system have been associated with endothelial dysfunction in cardiovascular diseases . Normal endothelium sustains vascular tone and structure by modulating the balance between vasodilators such as NO and prostacyclin, and vasoconstrictors such as endothelin-1 and angiotensin II . Reduced NO bioavailability, due to decreased NO production and/or increased NO inactivation, has been shown to aggravate endothelial dysfunction. The serine/threonine kinase Akt increases NO production by endothelial cells by activating eNOS .Oxidative stress causing impaired NO bioavailability also contributes to endothelial dysfunction. Decreased NO and oxidative excess may induce matrix metalloproteinases (MMPs), usually MMP-2 and MMP-9, which break down the fibrous cap containing collagen, elastin, and proteoglycans, resulting in endothelial dysfunction . Furthermore, plasma MDA and ADMA levels were effectively increased and plasma nitrate concentrations significantly reduced in patients with overt hypothyroidism, a mechanism closely implicated in endothelial dysfunction . Our findings suggest that chronic immobilization stress may cause endothelial dysfunction and systolic hypertension through vascular oxidative stress. Excess generation of ROS and oxidative stress has been implicated in endothelial dysfunction through the inactivation of NO. In this study, clary sage may play an important role in treating endothelial dysfunction by regulating oxidative stress and NO.
Clary sage treatment of rats subjected to immobilization stress contributed in recovery from endothelial dysfunction by decreasing oxidative stress and increasing NO production and eNOS expression. Appropriate concentrations of clary sage may result in recovery from endothelial dysfunction. These findings indicate that clary sage oil may be effective in the prevention and treatment of stress-induced cardiovascular diseases.
Systolic blood pressure
Endothelial nitric oxide synthase
Endemann DH, Schiffrin EL: Endothelial dysfunction. J Am Soc Nephrol. 2004, 15 (8): 1983-1992. 10.1097/01.ASN.0000132474.50966.DA.
Chung IM, Kim YM, Yoo MH, Shin MK, Kim CK, Suh SH: Immobilization stress induces endothelial dysfunction by oxidative stress via the activation of the angiotensin II/its type I receptor pathway. Atherosclerosis. 2010, 213 (1): 109-114. 10.1016/j.atherosclerosis.2010.08.052.
Grundt A, Grundt C, Gorbey S, Thomas MA, Lemmer B: Strain-dependent differences of restraint stress-induced hypertension in WKY and SHR. Physiol Behav. 2009, 97 (3–4): 341-346.
Grizzell JA, Iarkov A, Holmes R, Mori T, Echeverria V: Cotinine reduces depressive-like behavior, working memory deficits, and synaptic loss associated with chronic stress in mice. Behav Brain Res. 2014, 268C: 55-65.
Higashi Y, Noma K, Yoshizumi M, Kihara Y: Endothelial function and oxidative stress in cardiovascular diseases. Circ J. 2009, 73 (3): 411-418. 10.1253/circj.CJ-08-1102.
Tejovathi B, Suchitra MM, Suresh V, Reddy VS, Sachan A, Srinivas Rao PV, Bitla AR: Association of lipid peroxidation with endothelial dysfunction in patients with overt hypothyroidism. Exp Clin Endocrinol Diabetes. 2013, 121 (5): 306-309.
Gunnewich N, Higashi Y, Feng X, Choi KB, Schmidt J, Kutchan TM: A diterpene synthase from the clary sage Salvia sclarea catalyzes the cyclization of geranylgeranyl diphosphate to (8R)-hydroxy-copalyl diphosphate. Phytochemistry. 2013, 91: 93-99.
Seol GH, Lee YH, Kang P, You JH, Park M, Min SS: Randomized controlled trial for Salvia sclarea or Lavandula angustifolia: differential effects on blood pressure in female patients with urinary incontinence undergoing urodynamic examination. J Altern Complement Med. 2013, 19 (7): 664-670. 10.1089/acm.2012.0148.
Ou MC, Hsu TF, Lai AC, Lin YT, Lin CC: Pain relief assessment by aromatic essential oil massage on outpatients with primary dysmenorrhea: a randomized, double-blind clinical trial. J Obstet Gynaecol Res. 2012, 38 (5): 817-822. 10.1111/j.1447-0756.2011.01802.x.
Seol GH, Shim HS, Kim PJ, Moon HK, Lee KH, Shim I, Suh SH, Min SS: Antidepressant-like effect of Salvia sclarea is explained by modulation of dopamine activities in rats. J Ethnopharmacol. 2010, 130 (1): 187-190. 10.1016/j.jep.2010.04.035.
McDougall SJ, Paull JR, Widdop RE, Lawrence AJ: Restraint stress: differential cardiovascular responses in Wistar-Kyoto and spontaneously hypertensive rats. Hypertension. 2000, 35 (1 Pt 1): 126-129.
Spruill TM: Chronic psychosocial stress and hypertension. Curr Hypertens Rep. 2010, 12 (1): 10-16. 10.1007/s11906-009-0084-8.
Zicha J, Dobesova Z, Behuliak M, Pinterova M, Kunes J, Vaneckova I: Nifedipine-sensitive blood pressure component in hypertensive models characterized by high activity of either sympathetic nervous system or renin-angiotensin system. Physiol Res. 2014, 63 (1): 13-26.
Sugiura T, Kondo T, Kureishi-Bando Y, Numaguchi Y, Yoshida O, Dohi Y, Kimura G, Ueda R, Rabelink TJ, Murohara T: Nifedipine improves endothelial function: role of endothelial progenitor cells. Hypertension. 2008, 52 (3): 491-498. 10.1161/HYPERTENSIONAHA.108.111914.
Zafir A, Banu N: Induction of oxidative stress by restraint stress and corticosterone treatments in rats. Indian J Biochem Biophys. 2009, 46 (1): 53-58.
Harrison DG, Gongora MC: Oxidative stress and hypertension. Med Clin North Am. 2009, 93 (3): 621-635. 10.1016/j.mcna.2009.02.015.
Dimmeler S, Fleming I, Fisslthaler B, Hermann C, Busse R, Zeiher AM: Activation of nitric oxide synthase in endothelial cells by Akt-dependent phosphorylation. Nature. 1999, 399 (6736): 601-605. 10.1038/21224.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6882/14/396/prepub
This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (No.2012R1A2A2A02007145) and a Korea University Grant (2013).
The authors declare that they have no competing interests.
HJY and KYK performed the experiments, analyzed/interpreted data and drafted the manuscript. HSL and PK performed the experiments and analyzed/interpreted data. GHS contributed to the concept, designed experiments, analyzed/interpreted data and finalized the manuscript. All coauthors reviewed and discussed the paper. All authors read and approved the final manuscript.
Hyo Jung Yang, Ka Young Kim contributed equally to this work.
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Yang, H.J., Kim, K.Y., Kang, P. et al. Effects of Salvia sclarea on chronic immobilization stress induced endothelial dysfunction in rats. BMC Complement Altern Med 14, 396 (2014) doi:10.1186/1472-6882-14-396
- Salvia sclarea
- Chronic immobilization stress
- Endothelial dysfunction
- Oxidative stress