Fibrinolytic Compounds Isolated from a Brown Alga, Sargassum fulvellum

Two of bioactive natural products were founded in a brown alga, Sargassum fulvellum. After isolation and purification, the molecular structures of these two products were investigated by NMR spectroscopy and GC-mass spectroscopy. The two compounds were identified to be 1-O-palmitoyl-2-O-oleoyl-3-O-(α-D-glucopyranosyl) –glycerol (POGG) and 1-O-myristoyl-2-O-oleoyl-3-O-(α-D-glucopyranosyl) – glycerol (MOGG) which were obtained from Sargassum fulvellum for the first time. POGG and MOGG showed fibrinolytic activity in the reaction system of pro-u-PA and plasminogen.


Introduction
Algae living in a unique marine environment are more and more important in drug development because they metabolize many rare compounds via unknown pathway [1]. A number of studies illustrated that algae were important resource of natural drug development. For examples, the red alga Sphaerococcus coronopifolius showed antibacterial activity [2]; the green alga Ulva lactuca contained an anti-inflammatory compound [3]. Portieria hornemannii (Lyngbye) P.C. Silva was found to be a novel source of cytotoxic penta halogenated monoterpene, halomon, which has been selected for preclinical drug development since this compound shows toxicity to brain, renal and colon tumor cell-lines and preliminary evaluations in vivo have been encouraging [4]. Ulva fasciata produced a novel sphingosine derivative which has antiviral activity in vivo [5]. A cytotoxic metabolite, stypoldione, which inhibited microtubule polymerization and thereby prevented mitotic spindle formation, has been isolated from tropical brown alga, Stypopodium zonale [6]. An iodinated novel nucleoside has been isolated from Hypnea valitiae, which is a potent and specific inhibitor of adenosine kinase. It can be used in the studies of adenosine receptors in a variety of systems, and in studies on nucleotide metabolism and regulation [7]. Sargassum carpophyllum from the South China Sea is the source of two new bioactive sterols. These sterols induced morphological abnormality in the plant pathogenic fungus Pyricularia oryzae; also exhibited cytotoxic activity against several cultured cancer cell lines [8]. There are many algae that can convert simple polyunsaturated fatty acids, such as arachidonic acids, into complex eicosanoids and related oxylipins [9]. This conversation is very important because derivatives of arachidonic acids play role in maintaining homeostasis in mammalian systems and aberrant production of metabolites of this class occurs in diseases such as psoriasis, asthma, arteriosclerosis, heart disease, ulcers and cancer [7].
The perennial brown alga Sargassum fulvellum has a wide distribution in the East China Sea. A polysaccharide with antitumor activity from S. fulvellum was studied [10] in early time. Also, sulfated polysaccharides isolated from S. fulvellum were found to have antioxidant activity [11]. Kang et al. reported [12] that solvent extracts from S. fulvellum has antipyretic, analgesic, and anti-inflammatory activities in mice.
Researchers have found a lot of compounds from algae including glycosphingolipids, glycoglycerolipids, polyphenol phosphate glycoside and steryl glycoside. Among them, glucosyldiacylglycerol has been reported to have a few biological effects, including significant fibrinolysis [13,14], specific inhibition of tumor [15], and increased the cloning activation of phosphatidylserine decarboxylase in both the Bacillus subtilis null pss and psd mutants [16]. In this work, two of natural glucosyldiacylglycerol were isolated from a brown alga S. fulvellum using repeated chromatography with an open column of silica gel, and their structures and biological activities were investigated.

Results and discussion
S. fulvellum was selected by a screening of approximately 700 of plant extracts for compounds that enhance reciprocal activation of pro-u-PA and plasminogen. Specimen of S. fulvellum was collected from the East Sea in China and dried in natural environment. The dried samples were extracted by the mixture of methanol and chloroform. After removing the organic solvent, the residual was redissolved in chloroform and precipitated by the addition of acetone. The precipitate showing fibrinolytic activity was fractionated by repeated chromatography with an open column of silica gel and eluted with methanol and chloroform (proportion=3:7), to give compound 1 and compound 2. The yields of compound 1 and compound 2 from 200 g of brown alga were 25 mg and 15 mg, respectively.  The compound 1 was colorless. Its infrared spectrum presented characteristic absorption bands at 2920 cm -1 , 2852 cm -1 , 1742 cm -1 , 1219 cm -1 , 1171 cm -1 , 1035 cm -1 , and 771cm -1 . The positive-ion fast atom bombardment mass of the compound 1 gave the molecular weight with sodium ion at m/z 779  The existence of two fatty acid residues in the molecular structure of compound 1 were also identified from the wrap over 1 H and 13 C NMR signals in the range of 1.23~1.30 and 28.30~28.97 respectively. Methanolysis of the compound 1 yielded two methylated fatty acid, methyl palmitate and methyl oleate, which were identified by comparing the GC-MS results with those of authentic standards [17].
The glycosidic linkage between the glucose and glycerol was determined by glycosidation shift in 13 C-NMR and HMBC spectra, the chemical shift of C-1''' in glucose unit was at 98.3. Its proton was obviously correlated with the signal of C-3 in HMBC spectrum. In HMBC spectrum, two correlations were observed between the proton signal at δ4.21 (dd, J = 2.6, 12.1) or δ5.12 and the quaternary carbon signal at δ172.2 or δ172.4, suggesting the glycerol moiety was attached to C-1' or C-1" of the fatty moiety. The carbons and protons resonances of fatty residue moieties possess correlation, resulting in many cross peaks in 1 H-1 H COSY (Fig. 2) and HMBC spectrum (Fig. 3).    In the spectrum of positive-ion fast atom bombardment mass, palmitoyl moiety of ion peak at m/z 256 was most notable at 100% of fragment strength, suggesting it was strongly bombarded by electronic flow due to weak electronic shielding effect. Therefore, palmitoyl moiety was determined at C-1 because the electronic shielding role of C-1 was weaker than those of C-2 and C-3 as shown in the 13 C spectrum. Further, the oleoyl moiety was speculated at C-2.
Based on the above analysis of NMR data and mass spectra, the structure of the compound 1 was The pure compound 2 was also colorless. Its rate of flow (Rf = 0.30) was smaller than that of compound 1 (Rf = 0.48) when it was eluted using chloroform and MeOH (proportion=3:7) including 1% of acetic acid (V/V). Its characteristic absorption bands in infrared spectrum were similar to compound 1. The positive-ion fast atom bombardment mass of the compound 2 gave the molecular weight with sodium ion at m/z 718 [M+Na] + and mainly fragment ions at 212, which was identified to be myristoyl moiety by GC-MS. Table 2 presents the NMR data for compound 2 . By the similar analysis as compound 1, the compound 2 was determinated to be 1  ' 13.9 0.81 (6H, t, J = 6.7) The chemical shift is relative to DMSO-d 6 (δ C =39.5 ppm; δ H =2.49 ppm).
The coupling constant (J ) is given in Hz. The assignments of tow fatty acyl material are tentative and concomitantly interchangeable.
The fibrinolytic activities of compound 1 and 2 were investigated by the reciprocal activation of single chain urokinase-type plasminogen activator (pro-u-PA) and plasminogen. The addition of POGG (0.66-15.9 μM) or MOGG (0.66-5.28 μM) shortened the initiation time of pro-u-PA activation and increased the rate of activation in vitro (Fig. 4A, 4C), respectively. The dose-response curves were hyperbolic, and half-maximal effect were obtained approximately at 0.85μM of POGG (Fig. 4 B) and 1.3 μM (Fig. 4 D). These results illustrated that POGG and MOGG showed fibrinolytic activity in the reaction system of pro-u-PA and plasminogen, and MOGG exhibited weaker fibrinolytic activity than POGG. Pro-u-PA and plasminogen were incubated with the indicated concentrations of POGG and MOGG in the presence of Spectrozyme UK to determine reciprocal activation of pro-u-PA. Time course of the POGG and MOGG effect is shown in A, C and dose-response curve in B, D, respectively, in which the index for fibrinolytic activation is given in ordinate as percent of control value.

Conclusions
In this work, two of glucopyranosyldiacylglycerols, POGG and MOGG were isolated from the brown alga S. fulvellum, and there molecular structures were determined by NMR spectroscopy and mass spectroscopy. The extracts of S. fulvellum have been reported to have many biological roles, including antipyretic, analgesic, anti-inflammatory [12], antitumor [10] and antioxidant [11]. According to our knowledge, this is the first time to isolate MOGG from marine lives and discover that POGG and MOGG enhanced reciprocal activation of pro-u-PA and plasminogen in vitro.

General experimental procedures
Fast atom bombardment mass were determined with an assistant of trimethanolamine on a SX-102A mass spectrometer (JEOL USA Inc.). The infrared spectra were measured on a JIR-WINSPEC 50 FT-IR spectrometer (JEOL, Tokyo, Japan). 1 H-NMR (600 MHz), 13 C-NMR (150 MHz), and DEPT spectra were recorded on a JNM alpha 600 FT NMR spectrometer (JEOL, Tokyo, Japan) in dimethylsolfate-d 6 (DMSO-d 6 ), and chemical shifts are given in the  (ppm) scale, with coupling constants (J) in Hz with tetramethylsilane as a contrast standard. Procoated Kieselgel 60 F 254 cards (thickness 0.2 mm, Merck, Germany, No. 5450) were used to analysis of purification for thin layer chromatography using the solvent system of chloroform-methanol-acetic acid. Spot detection was conducted by spraying iodine vapor at room temperature.
The heteronuclear multiple quantum coherence (HMQC) experiment was carried out at 600.05 MHz with a sweep width of 4168.0 Hz and 2995.8 Hz. A 1.2-seconds relaxation delay was used and 64 transients were performed for each t 1 value.
The 1 H-1 H correlation spectroscopy experiment was carried out at 600.05 MHz with a sweep width of 4164.3 Hz and 2989.5 Hz. A 0.83-second relaxation delay was used and 16 transients were accumulated for each t 1 value.
The 1 H detected multiple bound connectivity experiment was carried out at 600.05 Hz with a sweep width of 4165.4 and 2995.8 Hz in F 1 and F 2 , respectively. The data set 512 points, and the mixing time 60 msec. The spectrum was recorded in the absorption mode.

Isolation of biophysiological substance
The compounds were extracted with chloroform-methanol (2:1) from S. fulvellum and isolated by repeated chromatography with silica gel columns. Briefly, dried S. fulvellum (200 g) was extracted twice with 900 ml of chloroform-methanol (2:1) and once with 900 ml of chloroform-methanol (1 : 2), and the organic extracts was evaporated to dryness, giving 15.1 g of oily residue. The residue was redissolved in 15.1 ml of chloroform, followed by the addition of 300 ml of acetone. The precipitate was collected by centrifugation. The precipitate (500 mg) was further fractionated by repeated chromatography with silica gel columns using solvent systems of chloroform-methanol and chloroform-methanol containing 1% acetic acid. Active component (15.1 mg) was recovered in a chloroform fraction in the final step.

Methanolysis of the compound
The compound 1 (3 mg) were dissolved in 1.5 ml of methanol solution (82%) containing 0.9 N of HCl. The solution was heated to 70 for 18 hours [21,22]. Then the solvent was evaporated to 0.1 ml under reduced pressure at 40 , followed by the extraction with hexane to yield an organic layer, which was purified using silica gel chromatography with elution of chloroform. The sample was dissolved in methanol for analysis by a JMS-GC Mate II (JEOL, Peabody, MA). A silica capillary GC column (30m 0.25mm, Agilent Technologies, Inc.) was used, and the column oven temperature was kept at 80 °C for 1 min after sample injection and then increased at a rate of 32 per min up to 150 , subsequently at a rate of 4 per min up to 250 , the flow rate of helium carrier gas was 1 ml/min. Identification of the peaks was accomplished by comparing the relative retention time and the mass spectra with those of standard fatty methyl esters.

Analysis of fibrinolytic activity
The fibrinolytic activities were determined in 50 μl of TBS/BSA (50 mM Tris-HCl, 100 mM NaCl and 2 mg/ml bovine serum albumin, pH 7.4) at 37℃ using a round-bottomed 96-well plate. The release of p-nitoaniline was measured serially for up to 120 min at 405 nm. The concentrations of pro-u-PA, plasminogen and Spectrozyme UK were as 20 nM, 5 nM and 100 μM, respectively.