Synthesis and lipid-lowering properties of novel N -(4-benzoylphenyl) pyrrole-2-carboxamide derivatives in Triton WR-1339-induced hyperlipidemic rats

One of the main risk factors that contribute to hyperlipidaemia is atherosclerosis and coronary heart disease. Therefore, researchers turn to synthesizing new compounds with potential lipid-lowering effects to overcome this issue. In the current study, Triton WR-1339 was used to induce hyperlipidaemia in the rat’s model. Moreover, we were able to synthesize, characterize, and validate a novel series of N -(4-benzoylphenyl) pyrrole-2-carboxamide derivatives; (compounds 3 and 5 ) and assess their potency as anti-hyperlipidemic agents. 300 mg/kg of triton WR-1339 was administered overnight intraperitoneally to fasted rats to urge hyperlipidemia and divided into five groups, control, hyperlipidemic, compounds 3 -, 5 -, and bezafibrate-treated rats. The pharmacological evaluation of compounds 3 and 5 at a dose of 15 mg/kg body weight showed that the elevated levels of plasma triglyceride, low-density lipoprotein cholesterol, and total cholesterol were significantly reduced after 18 hours of compounds 3 ( p < 0.001) and compound 5 ( p < 0.01) administration in comparison to the hyperlipidemic and control group at a given 15 mg/kg body weight dose. Moreover, it was noted that compounds 3 and 5 increased the high-density lipoproteins cholesterol levels significantly by 22% and 4.5% consecutively. Therefore, it can be concluded from these findings that N -(4-benzoylphenyl) pyrrole-2-carboxamide derivatives ( 3 and 5 ) have a definite antihyperlipidemic potential which could serve as protective agents against cardiovascular diseases and atherosclerosis


INTRODUCTION
The clinical manifestation (signs and symptoms) and progression of atherosclerosis and coronary heart disease are closely and significantly influenced by hyperlipidemia [1].In 2019, about 18 million people died from cardiovascular disease (CVD) globally [2].The major concern related to hyperlipidemia besides that it is not discovered until it reached threatening levels that it is an asymptomatic disorder of lipid metabolism with elevation in low-density lipoprotein cholesterol (LDL-C), serum total blood cholesterol [total cholesterol (TC)] and very LDL-C levels.
Hypercholesterolemia and hypertriglyceridemia (hyperlipidemic-associated lipid disorders) are considered to cause atherosclerotic CVD via implying abnormally increased levels of all lipids in the bloodstream [3].Atherosclerosis is defined as the building up of waxy plaque on the inner sides of the blood vessels [4,5].Atherosclerosisassociated diseases such as peripheral vascular, coronary, and cerebrovascular diseases are augmented in patients with hyperlipidemia [6].and 100.61MHz (C-13) using tetramethylsilane as an internal reference.
Despite that, there are a lot of different classes that act as antihyperlipidemic agents already exist.The most used class as an antihyperlipidemic globally are fibrates and their derivatives including bezafibrate.They act via the reduction of serum lipids, including a significant lowering in triglyceride (TG) levels with a slight decrease in TC, LDL-C, and elevation in the levels of high-density lipoprotein cholesterol (HDL-C) [10,11].Fibrates act by lowering the production of apoC-III and enhancing the action of lipoprotein lipase.While increased risk of atherosclerosis can be traced by triggering these markers [12,13].
Recently developing novel pharmacologically active lipid-lowering drugs have gained much interest in order to overcome the side effects and current medications and enhance the outcomes.Many studies on synthetic agents with pyrrole nucleus revealed encouraging pharmacological effects as anti-inflammatory [14,15], antitumor [16], antiviral [17], and antioxidative [18].In addition, regarding compounds containing pyrrole (ring) many researchers, which include our previous work, pointed out that these compounds compared to the others showed a very promising antihyperlipidemic effect [19][20][21].
Therefore, finding new possible agents that allow us to treat hyperlipidemia is highly important to lessen the threats of developing heart and blood vessel disease, the current research using a novel series of N-(4-benzoylphenyl) pyrrole-2-carboxamides aims to assess their ability to lower the lipid profiles (lipid-lowering-effect) in hyperlipidemic rats model using Triton WR-1339.

EXPERIMENTAL Materials and methods
All chemical agents were used without any further purifications and bought from (Sigma-Aldrich; St. Louis, MO, and Acros; Belgium).Melting point determination was done utilizing Stuart Scientific Electrothermal (melting point apparatus).Shimadzu IR Affinity-1 spectrophotometer was used to record infrared (IR) spectras.All samples were prepared as potassium bromide (Acros, Belgium) discs.Bruker DRX 400 MHz-NMR spectrophotometer operating at 400.13 ( 1 H) Blood samples were collected after 18 hours of treatment followed by immediate centrifugation at (3,000 rpm for 10 minutes).Enzymatic methods along with an automated analyzer (Model Erba XL-300, Germany, Mannheim) were used for the lipid analysis of the obtained serums.

Statistical analysis
The obtained data showed mean values ± standard error of the mean.The results were evaluated using Student's t-test, and a statistical probability of p < 0.05 was considered to be significant.

Novel
N-(benzoylphenyl)-pyrrole-2-carboxamide derivatives (3 and 5) were synthesized using substituted pyrrole ester and amino benzophenones as shown in Figures 1  and 2. Ethyl-substituted pyrrole-2-carboxylate (1 and 4b) was dissolved in DMF, followed by adding of 4-aminobenzophenone (2, 3M excess).The mixture was mixed and refluxed for 5 days at 150°C.A nucleophilic attack takes place by the free electrons of the N atom of the amine against the carbon of the carbonyl moiety of the ester derivative.Rearrangement of intermediate compound results in clicking out of an alcohol compound and amide bond formation as shown in Figure 3.
Amide formation was attempted under different conditions including free pyrrole acid with amino benzophenone, dicyclohexylcarbodiimide, and other amide coupling agents.Unfortunately, most of these conditions gave either lower yields or many side products that needed tedious chromatographic separation.Harsh conditions and heating at higher temperatures were major limitations since they led to hydrolysis of the starting materials and the formed products 3 and 5.
Before establishing the reaction condition for compounds 5, a neutralization procedure is needed as shown in Figure 2. The presence of HCl weakens the progress of the reaction.And it might affect the nucleophilicity of aminobenzophenone.TMA as the weaker base was used for (s, 2.0, 2H, NH 2 ), 1.90 (s, 3H, CH 3 ) ppm; 13

Animals experiment
The experiment was conducted on 2 months old male Wister rats, weighing 180-200 g, the study was done in agreement with the general guide for the care and use of laboratory animals in the Animal Care Center of the Faculty of Pharmacy, Al-Zaytoonah University of Jordan, Amman following Federation of European Laboratory Animal Science Associations guidelines [22].Rats were provided during the experimental duration (24 hours) with ad libitum access only to tap water.Rats were kept under a controlled 12-hour light/ dark cycle under controlled humidity and (22°C ± 2°C).All testing was approved by the local Ethical Committee of Animal Welfare.

Triton model of hyperlipidemia
Induction of acute hyperlipidemic animals was done via injecting Triton WR-1339 (Sigma-Aldrich, St. Louis, MO) 300 mg/kg body weight intraperitoneally (IP) to the rats [23].

Pharmacological experimental design
Forty overnight fasted rats were divided randomly into five groups each containing eight rats.
The first group got an IP administration of (normal) saline only and served as the control group (NCG); the second group received an IP injection of (Triton WR-1339) dissolved in distilled water representing the hyperlipidemic control group (HCG).Third and fourth group rats were IP injected with Triton, followed by an intragastric administration of (15 mg/ kg body weight) of compounds 3 and 5, respectively.The last group received intragastric injection of bezafibrate (100 mg/kg body weight) [24].Moreover, in compound 3 TC levels were significantly (p < 0.001) decreased by 75% and in compound 5 by 26% (p < 0.01) after 18 hours compared to HCG.Meanwhile, no significant changes were observed in TC levels after 18 hours in comparison to HCG in BF treated group (Fig. 5).After 18 hours of treatment, LDL-cholesterol levels dropped by (77%, p < 0.001) in compound 3 and (22%, p < 0.05) in compound 5.No noticeable changes in LDL-C levels were detected in bezafibrate (Fig. 6).
In fact, compounds 3 and 5 significantly decreased TG, TC, and LDL-cholesterol levels.In addition, compounds the liberation of the free amine since these conditions do not hydrolyze the pyrrole ester.
It's worth noting that due to the weakness of the aromatic amines; 4-amino-aminobenzophenone as nucleophiles, and the presence of the amine group on the para position of the carbonyl moiety of benzophenone decreases the nucleophilicity of the amine moiety.And, thus in turn affects the progress of the reaction for almost 5 days upon completion.

Induction of hyperlipidemia by Triton WR-1339
As we mentioned previously (Triton WR-1339) is used to induce acute hyperlipidemia in rats via inhibiting lipoprotein lipase enzyme which leads to blocking the clearance of TG-rich lipoproteins (TLRs).Triton WR-1339 was used in many studies to evaluate the efficacy of several antihyperlipidemic agents.It has been published before that one shot of (Triton WR-1339) IP at a dose of 300 mg/kg to adult rats is enough to produce acute hyperlipidemia and the (peak) plasma TG, LDL-C, and TC levels were reached at 18 hours [25].
Plasma levels of TC, TG, LDL-C, and HDL-C of the NCG and the HCG treated for 18 hours are shown in Table 1.
One shot of IP injection of Triton WR-1339 leads to a significant elevation in plasma TC, TG, and LDL-C (p < 0.0001) levels and a significant reduction in HDL-C (p < 0.0001) in HCG 18 hours after Triton injection compared to the NCG.The plasma TC levels in the HCG were markedly increased by 458%, after 18 hours as compared to the NCG.The increase of the TG levels in the HCG was 3911% in comparison with the NCG, which is about 40 times more than the TG levels in the NCG after 18 hours.LDL-C level in HCG was also raised by 612% after 18 hours as compared to the NCG at the same time, on the other hand, the HDL-C level was significantly reduced by 29% 18 hours after Triton WR-1339 injection.
Figures 4-7 show the effect of novel pyrrole carboxamide derivatives 3, 5, and BF on plasma TC, TG, HDL-C, and LDL-C levels in treated rats after 18 hours.Interestingly, the higher plasma TG levels produced by the single injection of Triton WR-1339 were remarkably (p < 0.001) decreased by 95% and 80% in compounds 3 and BF respectively, and by 23% in compound 5 (p < 0.001) after 18 hours, with respect to HCG treated with Triton (Fig. 4).The lipid-lowering activity of compounds 3 and 5 adds to the importance of the existence of the three structural components (heterocyclic aromatic ring able of hydrogen bond formation, large lipophilic moiety, and carboxamide linkage) for the anti-hyperlipidemic effects.These findings are compatible with our previously published data [32][33][34][35].

CONCLUSION
In the current study, novel N-(4-benzoylphenyl) pyrrole-2-carboxamide derivatives were successfully synthesized and distinguished using IR and NMR.The lipidlowering action was evaluated using hyperlipidemic rats induced by Triton WR-1339.N-(4-benzoylphenyl) pyrrole-2-carboxamide derivatives; compounds 3 and 5 were shown great potential in enhancing many lipid abnormalities such as hypercholesterolemia and hypertriglyceridemia, and then elevated HDL levels in Triton induced rats.These results are compatible with our previous published data, which approves that agents containing pyrrole-2-carboxamide nucleus do have a lipid-lowering effect [20].
In sum, our obtained result is highly encouraging with great potential, but more studies are required to explain the exact mechanisms of action and how the profile of these novel agents is secured and safe as (lipid-lowering) compounds.

PUBLISHER'S NOTE
This journal remains neutral with regard to jurisdictional claims in published institutional affiliation.The rise in plasma TG, TC, and LDL-cholesterol levels seen after a single injection of Triton is mainly due to Apoc3, Hmgcs1, Apob, and Apoa1 gene expression upregulation [26,27].Moreover, the large reduction in plasma HDL levels in Triton treated rats results mostly from the progressive movement of apolipoprotein A-1 from the HDL surface without loss of lipids [28].
Therefore, taking into consideration that ApoC3 is strongly linked to hypertriglyceridemia with an atherogenic effect and leads to hypertriglyceridemia by blocking the catabolism and the removal of TLRs [29,30], that's why it is not amazement that the hypolipidemic activity of compounds 3 and 5 was significantly higher for TGs than for cholesterol.These observations along with our previously published data on similar hypolipidemic agents suggest that our novel compounds 3 and 5 contribute by downregulating Apoc3 gene expression in acute hyperlipidemic rat model leading to decreased TG levels [31].

3 and 5
elevated serum HDL-C, and decreased the risk of atherosclerosis and cardiovascular disorders, after 18 hours of Triton administration.

Table 1 .
Effect of Triton WR-1339 on plasma lipid levels after 18 hours.