The Spice For Hypertension : Protective Role of Curcuma Longa

Untreated hypertension is a major cause for a variety of cardiovascular diseases, including coronary artery disease, heart failure, peripheral vascular disease, and stroke. Oxidative stress has been implicated in the development of hypertension. Elevation of blood pressure is attributed to an impairment between the balance of antioxidants and pro-oxidants. Over generation of free radicals causes a reduction in nitric oxide bioavailability. Eventually, this will increase total peripheral resistance and lead to endothelial dysfunction. Hypertension does not usually cause noticeable symptoms until it reaches the advanced stage to bring serious health problems with lifelong complications. Hypertensive patients are required to take medications for indefinite period of time to prevent further deterioration. Many of these therapeutic agents are expensive and may have unwanted adverse reactions. Curcuma longa (CL) or turmeric is one of the alternative herbs which confers medicinal properties. This review aims to summarise the effects of CL and its active constituents on blood pressure derived from preclinical and clinical published articles. Studies documented that CL and its active constituents could reduce blood pressure. These were achieved by antioxidant, anti-inflammatory activity, calcium (II) ion concentration interference, â2-adrenergic receptor activation, and renin-angiotensin system inhibition. There is a potential role of CL in the management of hypertension. However, limited studies of CL have been conducted on human. Thus, more well-planned studies should be carried out to ascertain its effectiveness.

High blood pressure (BP) or hypertension is considered as the prevalent risk factor for the pathogenesis of cardiovascular diseases (CVD) such as myocardial infarction, stroke, and cardiac failure. 1,2One of the major health challenges in developing and developed nations today is the high incidence and rapidly growing problem of hypertension, especially among the elderly; with increased risk of all-cause mortality. 3,4ccording to the Eight Report of the Joint National Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure (JNC 8), a person who is diagnosed of having hypertension has been redefine to have systolic blood pressure (SBP) between 130 and 139 mm Hg or diastolic blood pressure (DBP) ranging 80 to 89 mm Hg. 5 This new threshold would lead to more people to be categorised as having hypertension compared to the previous BP reading in JNC 7, 140  to 159 mm Hg and 90 to 99 mm Hg for SBP and DBP, respectively. 6Under JNC 8 classification for hypertension, those with clinical CVD are required to take medications and accompanied by lifestyle changes. 5herefore, it is better to prevent than to cure with long-term antihypertensive medications.
Prolonged intake of medications is often associated with undesired side effects.Hence, this has prompted the researchers to explore alternative treatment with comparable efficacy, affordable cost, and minimal adverse effects.Interest and demand for using plant-based traditional medicines in treating and preventing CVD have been growing.The reason may be attributed to easy availability, efficacy and cultural acceptability.Curcuma longa (CL), or commonly known as turmeric, originates from southeast India and is extensively cultivated in tropical areas of South Asia.It is a herbaceous perennial plant in the ginger family, known as Zingiberaceae.Its aromatic tuberous rhizome has been widely used in medicinal, culinary and dyeing purposes. 7urmeric has been used as a food colour additive and a dyeing agent in textile industry due to its distinct yellow colour.It is mainly consumed in curry dishes.In addition, it is available in different forms for various uses such as drinks, capsules, tablets, powder, ointments, and soaps. 8Curcumin extracted from the rhizome has been documented to exhibit potent pharmacological properties such as antioxidant, 9,10 anti-inflammatory, 11,12 a n t i m i c r o b i a l , 13,14 a n t i c a r c i n o g e n i c , 15,16 hypoglycaemic, 17 and hepatoprotective effects. 18hus, the aim of this review paper was to examine the current evidence on the cardiovascular protective effects of CL against hypertension in addition to the possible mechanisms underlying these beneficial effects.

Literature Search
Literature search was performed with two online databases, namely PubMed and Scopus using keywords "curcumin" OR "Curcuma longa" OR "curcuminoids" AND "hypertension".The electronic search was carried out from 1 st July 2018 to 31 st July 2018.Relevant original research articles written in English were retrieved.Preclinical and clinical studies were included in this review.

Curcuma longa (CL)
Among the Curcuma species, CL has the highest amount of curcuminods. 19he three main curcuminoids found in the CL are curcumin, demethoxycurcumin and bisdemethoxycurcumin. 20,21 Among these curcuminoids, curcumin has been studied extensively.Curcumin is poorly absorbed when given orally.Although curcumin has low oral bioavailability, it possesses pronounced biological activities.][24] The effects of CL on blood pressure in animal studies Goto et al. evaluated the effect of yellow turmeric, CL and white turmeric, Curcuma zedoaria (CZ) on vasomotion and haemorheology in adult male spontaneous hypertensive rats (SHR). 25The animals were fed with normal rat chow or chow fortified with 3% weight/weight (w/w) of CL, 1% w/w of CZ, 3% w/w of CZ or 100 mg/kg/day of captopril in drinking water, respectively for 12 weeks of study duration.It was reported that 3% w/w of CZ was more effective as a hypotensive agent than CL.This is because the latter merely showed a trend in reducing SBP while the former with a significant reduction of SBP compared to the control group.In addition, ingestion of 3% w/w of CZ showed a greater increment in endotheliumdependent relaxation following addition of acetylcholine (ACh).Captopril, a positive control showed a similar pattern of activities.On the other hand, rats fed with 3% w/w of CZ diet exhibited a marked reduction in aortic contraction in response to xanthine oxidase.This enzyme is responsible for the production of reactive oxygen species (ROS).Both 3% w/w of CL and CZ groups significantly reduced the low shear stress of whole blood viscosity.However, this protective effect was not observed in the rats given with captopril.
Hypotensive and vasorelaxant activities of the methanolic extract of CL (MECL) were studied in male Wistar normotensive rats. 26The mean arterial pressure was significantly reduced at the given dosage of 20 mg/kg and 30 mg/ kg.Meanwhile, the heart rate was significantly reduced in a dose-dependent manner starting from 1 mg/kg to 30 mg/kg of MECL administered intravenously.The increasing concentration of MECL from 1 µg/mL to 1000 µg/mL attenuated the pre-contraction induced by phenylephrine (PE, 10 µM) and potassium chloride (KCl, 80 mM) in both the intact and denuded isolated superior mesenteric rings.Adaromoye et al. then conducted a series of experiment to investigate the possible mechanism of vasorelaxation induced by MECL. 26Endothelium denuded mesenteric rings were pre-contracted with PE after being pre-incubated with four different agents, namely glibenclamide (10 µM), barium chloride (1 mM), tetraethylammonium (1 mM) and 4-aminopyridine (1 mM), respectively to inhibit potassium ion (K + ) channels.However, these inhibitors did not affect the vasorelaxation induced by the increasing concentration of MECL in the rings pre-contracted with PE.
Effect of MECL on contraction induced by calcium chloride (CaCl 2 , 1 µM to 10 mM) also being examined. 26It was reported that CaCl 2 evoked contraction in a concentration-dependent manner.Presence of MECL from 1 µg/mL to 1000 µg/mL significantly suppressed the contraction in response to CaCl 2 .In order to determine whether the MECL could disturb calcium (II) ion (Ca 2+ ) release intracellularly, the denuded mesenteric rings were pre-contracted with KCl (60 mM) in a Ca 2+ -free medium.Additionally, the rings were eventually exposed to PE (10 µM) or caffeine (20 mM). 26The induced-contractile responses were then evaluated with the cumulative concentration of MECL.The obtained results revealed that MECL was able to attenuate the transient contraction evoked by PE in endothelium-denuded mesenteric rings.However, the similar findings were not to be observed when tested with caffeine.
Hlavaèková et al. performed a study to determine the effects of curcumin and combination of curcumin and piperine on the BP and aorta remodelling in adult male Wistar rats. 27ypertension was induced by administration of Nù-nitro-L-arginine methyl ester hydrochloride (L-NAME).The BP was measured weekly and the isolated thoracic aorta was stained for morphological examination.The increased of BP by L-NAME was partially prevented by administration of 100 mg/kg/day of curcumin.Despite of that, combination of curcumin and piperine showed less significant results on BP.Curcumin was reported to reduce the myofibrils and increase the actin as well as the elastin content in the aortic media of the nitric oxide (NO)-deficient rats.Thus, curcumin was more capable than concurrent use of curcumin and piperine to prevent aorta remodelling with morphological changes in the vascular wall induced by hypertension.
Tetrahydrocurcumin (THC) is one of the major metabolites of curcumin.Adult male Sprague-Dawley rats were fed with L-NAME in drinking water for three weeks. 28Curcumin or THC (50 mg/kg/day and 100 mg/kg/day) was fed to the rats simultaneously with L-NAME.Both curcumin and THC decreased BP, vascular resistance and improved vascular responsiveness in hypertensive rats.Moreover, curcumin or THC reduced the plasma levels of malondialdehyde (MDA) and protein carbonyl in hypertensive rats as well as the production of superoxide in the aorta.Besides, both curcumin and THC were able to prevent the depletion of blood glutathione (GSH) and to restore the redox status of the L-NAME-treated rats.Treatment with curcumin or THC also increased endothelium nitric oxide synthase (eNOS) protein expression in aorta and plasma nitrate/nitrite level.Interestingly, the antihypertensive and antioxidant effects of THC was greater than curcumin.
In another study by Nakmareong et al., the rats were given L-NAME for five weeks instead of three weeks. 29Furthermore, a dose of 50 mg/kg/ day or 100 mg/kg/day of THC was intragastrically administered to the rats at the last two weeks once the hypertensive stated had been established with L-NAME.The same parameters were carried out as performed by Nakmareong et al. 28 However, Nakmareong et al. tested the aortic elasticity 29 instead of aortic reactivity 28 .The findings obtained in this study 29 were in agreement with the earlier study 28 .In addition, THC reduced thoracic aortic wall thickness and stiffness in the rats receiving L-NAME.THC, especially the higher dose showed a greater protective action in hypertensive rats. 28,29espite of that, both doses of THC or curcumin had no effect on normotensive rats. 28,29These obtained results confirmed the deficiency of NO production, which eventually led to the elevation of BP following administration of L-NAME.
Hypertension was induced in male Sprague-Dawley rats by clipping their left renal artery with a silver clip, hence a 2 kidney-1 clip (2K-1C) model was used.The rats were gavaged with two different doses of curcumin (50 mg/ kg/day and 100 mg/kg/day) for six weeks. 30t the end of the treatment, curcumin reduced hindlimb vascular resistances and arterial BP as well as increased hindlimb blood flow in 2K-1C hypertensive rats.There was an impairment of endothelium-dependent vasorelaxation in response to ACh when tested on isolated thoracic aortic rings from hypertensive rats compared to the sham control groups.However, administration of curcumin increased the relaxant activity in a dose-dependent manner.Treatment with or without curcumin either in the sham or hypertensive groups did not affect the endothelium-independent relaxation elicited by sodium nitroprusside.The endothelial dysfunction in the 2K-1C hypertensive rats was restored by curcumin with the increased of plasma nitrate/nitrite levels and e-NOS protein expression in the thoracic aorta.Furthermore, curcumin treatment ameliorated the increased of superoxide production in the carotid artery and the oxidative stress markers such as MDA and protein carbonyl in the plasma of 2K-1C rats.
This renovascular hypertension caused an elevation in the plasma angiotensin-converting enzyme (ACE) level accompanying with an increase of a regulatory subunit of reduced form of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, p47 phox in thoracic aorta. 30In contrast, administration of curcumin shown a reduction in both the ACE level and the protein expression of p47 phox NADPH oxidase subunit.Boonla et al. also revealed that hypertension induced structural changes and remodelling in thoracic aorta of the 2K-1C rats. 30Aortic wall hypertrophy and hyperplasia were observed in parallel with the increased of smooth muscle actin, collagen and elastin contents.In addition, there was an increase of matrix metalloproteinases (MMP) levels including MMP2 and MMP9 in the aorta of the 2K-1C hypertensive rats.Curcumin significantly reversed the abnormalities of vascular structure and remodelling in this study.The protective effect of curcumin follows a dosedependent manner, especially the higher dose which exhibited a greater beneficial action in 2K-1C hypertension.
Akinyemi et al. investigated the effect of CL on ACE and arginase activities in adult male Wistar rats. 31The rats were induced by L-NAME for 10 days to become hypertensive.The rats were assigned into five groups: normotensive control, hypertensive, hypertensive with atenolol (â 1 -adrenergic receptor antagonist), normotensive with CL and hypertensive with CL, respectively.The study duration was 24 days.Administration of L-NAME caused a significant increase in SBP compared to the normotensive rats.On the other hand, rats fed with diet supplemented with 4% of CL or 10 mg/kg/day of atenolol was able to reduce SBP as compared to the hypertensive rats.Furthermore, pretreatment with CL for 14 days led to a significant inhibitory effect on ACE and arginase activities in the serum and kidney.In addition, CL increased NO level and decreased serum creatinine and urea levels.
With the same experimental protocol, Akinyemi et al. tested the effect of CL on platelets ectonucleotidase and adenosine deaminase (ADA) activities 32 , as well as inflammatory cytokines and enzyme activities of cholinergic and purinergic systems 33 .Intake of CL caused a reduction in adenosine triphosphate (ATP) hydrolysis and ADA but an elevation in adenosine diphosphate (ADP) and adenosine monophosphate (AMP) hydrolysis. 32Pretreatment with CL reduced the serum pro-inflammatory cytokines (interleukin-1, interleukin-6, tumour necrosis factor-á and interferon-ã) and increased in anti-inflammatory agent (interleukin-10) levels. 33Akinyemi et al. reported that acetylcholinesterase activity in peripheral lymphocytes was significantly reduced by CL. 33 Likewise, serum butyryl-cholinesterase activity was clearly decreased by CL in rats receiving L-NAME. 33Ectonucleoside triphosphate phosphohydrolases (NTPDases) activities using ATP and ADP as substrates and ADA activity in peripheral lymphocytes were also found to be reduced following the supplementation of CL. 33 Li et al. shown that treatment with 10 mg/kg/day of demethoxycurcumin (DMC) for three weeks decreased the SBP in 30-week-old male SHR. 34In addition, long-term administration of DMC was able to diminish the increased endothelium-dependent contraction by ACh and enhance the reduced ACh-induced relaxation in the renal arteries of SHR.It was reported that phosphorylation of endothelium nitric oxide synthase (P-eNOS) and cyclooxygenase 2 (COX-2) protein expression were reduced and elevated, respectively in renal arteries from SHR.Those changes were corrected by the treatment of DMC for three weeks.Therefore, DMC may play an important role in contributing to the improvement of endothelial function in hypertension by reducing COX-2 expression.
Xia et al. reported that curcumin treatment significantly decreased the BP of male albino rats in a dose-(60 mg/kg/day and 120 mg/kg/day) and time-(14 days and 28 days) dependent manner. 35he rats undergone surgical operation to produce cranial window.Curcumin significantly increased red blood cell velocity, microvascular diameter, vasomotion and number of open capillaries.On the other hand, circulating endothelial cells were reduced following curcumin administration.The obtained results suggested that curcumin was able to maintain endothelium integrity.Furthermore, by increasing the number of open capillaries, this in turn can reduce the peripheral resistance and eventually decrease the BP in rats receiving curcumin.The rise in vasomotion as in amplitude and frequency, led to an increase of blood flow, which may be useful for curcumin to regulate the cerebral microcirculation in hypertension.
Adult male 8-week old C57BI/6J mice were used by Yao et al. to determine the effect of curcumin on angiotensin II (Ang II)-induced hypertension. 36The animals were divided into three groups, namely control, Ang II (490 ng/min/ kg; subcutaneously) and Ang II with curcumin (300 mg/kg/day; oral gavage).After one week of treatment, curcumin was shown to reduce SBP and DBP in Ang II-treated mice.In addition, curcumin suppressed the contractions of mesenteric arteries in response to the increasing concentration of Ang II (10 -9 M to 10 -5 M).Moreover, curcumin also decreased the expression of angiotensin II type 1 receptor (AT 1 R) protein expression in thoracic aorta of Ang II-induced hypertensive mice.Based on the obtained results, curcumin may exert its inhibitory effect on hypertension by reducing AT 1 R expression as well as to attenuate vasoconstriction elicited by Ang II.
Overall, animal studies in general show a protective effect of CL or its constituents on BP (Table 1).CL or its constituents can be used as an individual treatment to inhibit increased of BP in animals.Combination of curcumin and piperine has been evaluated for their preventive effects on BP.Piperine was shown to increase bioavailability of curcumin. 37Nevertheless, curcumin alone demonstrated a greater beneficial effect than co-administered with piperine in reducing BP. 27 Hypertension is multifactorial in nature.The antihypertensive effects of a particular drug are not able to be fully explained by using one animal model.There are many pathways which responsible for the development of BP dysregulation.Therefore, various experimental models such as genetic hypertension, environmental hypertension, pharmacological hypertension and renal hypertension have been employed to evaluate the antihypertensive action of CL or its constituents.The dose of CL or its constituents used in the aforementioned studies varies greatly.The common administered doses are 50 mg/kg/day and 100 mg/kg/day.None of the studies reported any adverse reactions suffered by the laboratory animals.

The effects of CL on blood pressure in human studies
Thirty-nine healthy middle-aged and older adults with mostly Caucasians were divided into placebo (n = 19) and curcumin supplemented groups (n = 20) for 12 weeks by Santos-Parker et al. 38 Ingestion of 2000 mg/day of curcumin (Longvida® pill) improved endothelial function of resistance and conduit arteries in these healthy middle-aged and older adults.Intake of curcumin was shown to reverse the reduction in forearm blood flow following infusion of ACh in the presence of L-NAME, a NOS inhibitor.In addition, 12 weeks of curcumin reduced oxidative stressmediated suppression of endothelium-dependent vasodilatation in response to co-administration of antioxidant vitamin C. The protective action may be due to the ability of curcumin to increase NO bioavailability and reduce oxidative stress.However, there was no difference in BP between placebo and curcumin treated groups.The possible reason is curcumin has no hypotensive effect on normal healthy subjects.Choi et al. (2018) analysed data from the Korean National Health and Nutrition Examination Survey (KNHANES) 2013 to investigate the effect of curry consumption in reducing hypertension. 39his cross-sectional study involving 1350 relatively healthy subjects were divided into curry intake group (n = 603) which had consumed a curry dish more than once a month over the previous year, and non-curry intake group (n = 747).The most common curry powder available in the market of South Korea is 10% of total 20 g portion per person.This amount equivalent to about 2 g of CL with 1 mg to 11.5 mg of curcumin present in the curry powder. 39However, due to the nature of this study, detailed information regarding to the  Choi et al. revealed that subjects consumed curry regularly had a lower odd ratio for the prevalence of hypertension than those without consumed curry. 39However, when age, sex, smoking and body mass index were adjusted, only the noncurry intake group showed significant odd ratio for the prevalence of hypertension.These findings indicated that the presence of other factors may have an impact on the relations in the curry intake group.

Possible Pharmacological Actions of CL against Hypertension
The precise mechanism on how CL reduces BP is not exactly known.The antihypertensive effects of CL may be attributed to the active compounds, each with distinct mechanisms of actions.Several possible mechanisms involved in BP reduction are suggested, which include antioxidant, anti-inflammation, Ca 2+ concentration interference, â 2 -adrenergic receptor stimulation, and renin-angiotensin system inhibition (Figure 1).Oxidative stress has been linked to the pathogenesis of hypertension.Oxidative stress occurs when there is a disturbed balance between the levels of antioxidant and pro-oxidant.Impaired defence mechanism of antioxidant coupled together with over production of free radicals leads to cell damage.ROS such as superoxide will react with NO to generate peroxynitrite, a potent prooxidant.NO contributes to the maintenance of vascular homeostasis by causing vasodilatation, and reducing total peripheral resistance.
Curcumin is known for its strong antioxidant property.Methanolic extract of CL (200 mg/kg/day) was gavaged to the male Wistar rats prior to the administration of L-NAME for three weeks. 40Rats in L-NAME group showed a significant increase in serum urea, creatinine kinase and alanine aminotransferase levels.Furthermore, lipid peroxidation was augmented in the liver, heart and kidney isolated from the L-NAMEtreated rats.Supplementation of CL caused a significant reduction of these biochemical indices in rats receiving L-NAME.Generation of lipid peroxidation products might be due to the reduced activities of enzymatic antioxidants as observed in this study.L-NAME greatly reduced the levels of hepatic catalase, superoxide dismutase (SOD), glutathione S-transferase, GSH as well as renal SOD and GSH.In contrast, pretreatment with CL restored the reduced antioxidant activities in L-NAME group to a level similar to the control that received only corn oil as a drug vehicle.
Lekshmi et al. conducted a study to investigate the effects of CL against cellular and low-density lipoprotein (LDL) cholesterol oxidation. 41In this study, fresh rhizomes of CL were extracted with hexane, ethyl acetate, methanol, and water, respectively.Ethyl acetate extract was demonstrated to exhibit the highest 2, 2'-diphenyl-1-picrylhydrazin (DPPH), 2, 2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS), hydroxy and superoxide radical scavenging capacity compared to other tested extracts.In addition, ability of CL to reduce oxidative stress in cells was reported.Immortalised mouse myoblast cell line, C2C12 cells were used to induce oxidative stress using hydrogen peroxide.Ethyl acetate, methanol and water extracts showed a concentration-dependent reduction in cellular oxidative stress.The experimental concentration of 100 µg/mL of ethyl acetate was revealed to be comparable to the 25 µg/mL of ascorbic acid used as a positive control.Furthermore, ethyl acetate, methanol and water extracts were effective in inhibiting LDL cholesterol oxidation in a concentration-dependent manner.Interestingly, ethyl acetate extract was reported to be 40 times more effective than ascorbic acid.The capability of the extracts was suggested to be attributed to the presence of phenolics and curcuminoids.
ACE is the key enzyme converting Ang I to Ang II, a potent vasoconstrictor in regulating cardiovascular homeostasis.Ang II induces oxidative stress via activation of nicotinamide adenine dinucleotide/nicotinamide adenine dinucleotide phosphate (NADH/NADPH) oxidase and the production of ROS. 42Moreover, Ang II enhances lipid peroxidation 43 and promotes the synthesis of pro-oxidant cytokines, 44,45 which cause a rise in the BP.Ang II decreases the expression of NOS. 42The Ang II-induced superoxide formation scavenges NO and reduces NO bioavailability. 46onsequently, this could lead to endothelial dysfunction. 46he antihypertensive activity of CL was examined by measuring its inhibitory activity on ACE by using hexane, ethyl acetate, methanol and water extracts. 41Ethyl acetate (IC 50 = 0.06 µg/mL) extract had the highest ACE inhibitory capability followed by methanol (IC 50 = 0.19 µg/mL) and water (IC 50 = 0.38 µg/mL) extracts.However, hexane extract did not show any measurable inhibitory potential.All the three extracts (ethyl acetate, methanol and water) were more potent compared to captopril (IC 50 = 6.28 µg/mL), an ACE inhibitor which is commonly prescribed for hypertensive patients.
Yao et al. investigated the effect of curcumin on AT 1 R expression using embryonic thoracic aortic smooth muscle cells, A10 cells. 36urcumin was found to decrease the AT 1 R protein expression in a concentration-(10 -5 M to 10 -9 M) and time- (2, 6, 8, 16, 24, 30 h) dependent manner.Furthermore, curcumin reduced AT 1 R mRNA expression as determined by reverse transcription polymerase chain reaction (RT-PCR).Eventually, Yao et al. proceeded the experiment by treating A10 cells with cycloheximide to block de novo protein synthesis and actinomycin D to block de novo mRNA synthesis.Both of these drugs did not have inhibitory effect on curcumin in terms of its role in down-regulating the AT 1 R expression.The obtained results suggested that curcumin may down-regulate the expression of AT 1 R at the transcriptional level.
In order to elucidate the underlying mechanism of how the curcumin regulates the AT 1 R gene expression, Yao et al. used five deletion mutants of rat AT 1 R promoter region ligated to the luciferase gene. 36The deletion mutants of the AT 1 R promoter caused a reduced promoter activity.This AT 1 R promoter activity was inhibited by curcumin.The findings proposed that the curcumin inhibited AT 1 R expression at the transcriptional level and that proximal element of the AT 1 R promoter was vital for the down-regulation of AT 1 R by curcumin.At the same time, Yao et al. found that curcumin decreased specificity protein 1 (SP1) binding to the AT 1 R promoter in A10 cells.This shown the important role of ubiquitous transcription factor SP1 for the regulation of AT 1 R expression.
Human umbilical vein endothelial cells (HUVECs) were cultured and treated with Ang II (1 µmol/L) for 12 hours with the presence or absence of demethoxycurcumin (DMC; 10 µmol/L). 34DMC is one of the major curcuminoids found in CL.Li et al. revealed that Ang II caused a reduction in NO generation in HUVECs by decreasing A23187 which served as a calcium ionophore to activate P-eNOS.Western blot assays demonstrated that down-regulation of P-eNOS expression in HUVECs treated with Ang II was to be reversed by the addition of DMC.Similar results were obtained with the addition of celecoxib, a COX-2 inhibitor or losartan, an AT 1 R blocker.Following the normalisation of P-eNOS expression, DMC, celecoxib and losartan were able to restore the NO production in HUVECs.
Nuclear factor kappa B (NF-êB) plays a pivotal role in regulating transcription by mediating inflammation, immune and stress responses.In addition, NF-êB also regulates cell development, differentiation, proliferation and apoptosis.NF-êB is to be activated upon stimulation by pro-inflammatory cytokines.It is an inducible cell transcription factor and a key regulator in the production of COX-2.Previous studies have documented that CL was able to inhibit NF-êB pathway and resulted in a reduction of cytokines and COX-2 expression. 47,48enal arteries from normotensive and hypertensive patients undergoing radical nephrectomy were obtained by Li et al. 34 The arteries from hypertensive patients were cultured for 12 hours with or without DMC (10 µmol/L).Both Western blot assay and immunofluorescence microscopy revealed that the COX-2 expression was higher for hypertensive than normotensive patients.The increased COX-2 protein expression was to be depressed with the presence of DMC.Li et al. also conducted an in-vitro study to observe the effect of DMC on isolated renal arteries from SHR. 34 The arteries exhibited a reduced endothelium-dependent relaxation in response to ACh.However, a greater contraction by ACh was observed when the arteries were pre-incubated with L-NAME which acted as an inhibitor of NOS.These altered vascular responses were not that severe in the normotensive Wistar-Kyoto rats.The renal arteries exposed to DMC (10 µmol/L) for 12 hours enhanced relaxation as well as suppressed contraction induced by ACh.Treatment with celecoxib also produced similar findings.The COX-2 protein expression was down-regulated following to the exposure of DMC for 12 hours.
Moohammadaree et al. explored the vasorelaxant effect of hexahydrocurcumin (HHC), a metabolite of curcumin, using isolated thoracic aorta from male Wistar rats. 49It was shown that cumulative concentration of HHC ranging from 1 nM to 1 mM attenuated the contraction induced by PE (10 µM) or KCl (80 mM).There was no difference of vasorelaxant response observed between the endothelium-intact and endotheliumdenuded aortic rings.This obtained results may indicate that HHC induced vasorelaxation via an endothelium-independent mechanism by acting directly on the vascular smooth muscle cells.Ability of HHC to relax aortic rings precontracted with either PE or KCl may suggest an inhibition of extracellular Ca 2+ influx.In addition.preincubation with HHC (0.1 µM, 1 µM, 10 µM and 100 µM) suppressed sustained contraction evoked by increasing concentration of CaCl 2 (10 µM to 10 mM) and transient contraction induced by PE (10 µM) or caffeine (20 mM) in Ca 2+ -free Krebs solution.Therefore, HHC may exhibit inhibitory activity on Ca 2+ mobilisation from internal stores.
Furthermore, increasing concentration of HHC (1 nM to 1 mM) was reported to abolish contractile response induced by phorbol 12-myristate 13-acetate (PMA, 1 µM) which activates protein kinase C (PKC).PKC has been demonstrated to modulate vascular contraction through direct phosphorylating myosin light chain kinase. 50HHC-evoked vasorelaxation may involve an inhibition of PKC mediated Ca 2+ -independent contraction.Aside from that, pretreatment with propranolol (1 µM)), a nonselective â-adrenergic receptor antagonist, caused a reduction in vasorelaxation elicited by HHC.Stimulation of â 2 -adrenergic receptor leads to an activation of adenylyl cyclase and an increase in the intracellular cyclic adenosine monophosphate levels. 51When â 2 -adrenergic receptor is blocked by propranolol, HHC is not able to stimulate the receptor to produce vasorelaxation.Hence, HHC may produce vasorelaxant activity via an agonistic effect on â 2 -adrenergic receptor.

ConCLuSion
CL has been used as a traditional medicine for various ailment without causing further detrimental effects in human.Previously, CL has been documented to exert beneficial action on cancers in the clinical trials.Noncommunicable disease is one of the causes with high mortality rate.Since hypertension is a risk factor of CVD, further well-designed studies should be performed to confirm the efficacy of CL on human population.It is an important area for further research and development to combine CL with other antihypertensive drugs to investigate their possible synergistic effects and preferable pharmacological properties in reducing BP.In addition, pharmacokinetic profiles of CL should be improved in view of its low oral bioavailability and rapid metabolism.This in turn can increase the product value and further expand its market in the pharmaceutical industry.

Table 1 .
Effect of Curcuma longa (CL) and its constituents on blood pressure (BP) in animal model