Author(s): Shaaban M, Abd-Alla HI, Hassan AZ, Aly HF, Ghani MA
Background: More than 15,000 marine products have been described up to now; Sponges are champion producers, concerning the diversity of products that have been found. Most bioactive compounds from sponges were classified into anti-inflammatory, antitumor, immuno- or neurosurpressive, antiviral, antimalarial, antibiotic, or antifouling. Evaluation of in vitro inhibitory effects of different extracts from four marine sponges versus some antioxidants indices and carbohydrate hydrolyzing enzymes concerned with diabetes mellitus was studied. The chemical characterizations for the extracts of the predominating sponges; SP1 and SP3 were discussed.
Methods: All chemicals served in the biological study were of analytical grade and purchased from Sigma, Merck and Aldrich. All kits were the products of Biosystems (Spain), Sigma Chemical Company (USA), Biodiagnostic (Egypt). Carbohydrate metabolizing enzymes; α-amylase, α-glucosidase, and β-galactosidase (EC3.2.1.1, EC3.2.1.20, and EC3.2.1.23, respectively) were obtained from Sigma Chemical Company (USA).
Results: Four marine sponges; Smenospongia (SP1), Callyspongia (SP2), Niphates (SP3), and Stylissa (SP4), were collected from the Red Sea at Egyptian coasts, and taxonomically characterized. The sponges' extracts exhibited diverse inhibitory effects on oxidative stress indices and carbohydrate hydrolyzing enzymes in linear relationships to some extent with concentration of inhibitors (dose dependant). The extracts of sponges (3, 1, and 2) showed, respectively, potent-reducing power. Purification and Chemical characterization of sponge 1 using NMR and mass spectroscopy, recognized the existence of di-isobutyl phthalate (1), di-n-butyl phthalate (2), linoleic acid (3), β-sitosterol (4), and cholesterol (5). Sponge 3 produced bis-[2-ethyl]-hexyl-phthylester (6) and triglyceride fatty acid ester (7).
Conclusion: Marine sponges are promising sources for delivering of bioactive compounds. Four marine sponges, collected from Red Sea at Egyptian coasts, were identified as Smenospongia (SP1), Callyspongia (SP2), Niphates (SP3), and Stylissa (SP4). The results demonstrated that different sponges extracts exhibited inhibitory effects on oxidative stress indices and carbohydrate hydrolyzing enzymes in linear relationships to some extent with concentration of inhibitors (dose dependant). The extracts of sponges (3, 1, and 2) showed, respectively, potent-reducing power. Chemical characterizations of sponges SP1 and SP3 were discussed. Based on this study, marine sponges are considered as talented sources for production of diverse and multiple biologically active compounds.
Referred From: https://www.ncbi.nlm.nih.gov/pubmed/22898269
Author(s): Haefner B
Author(s): Belarbi el H, Contreras Gómez A, Chisti Y, García Camacho F, Molina Grima E
Author(s): Sipkema D, Franssen MC, Osinga R, Tramper J, Wijffels RH
Author(s): Alcaraz MJ, Payá M
Author(s): Paul VJ
Author(s): Green G
Author(s): Proksch P
Author(s): Taylor MW, Radax R, Steger D, Wagner M
Author(s): Stowe SD, Richards JJ, Tucker AT, Thompson R, Melander C, et al.
Author(s): Thompson JE, Walker RP, Faulkner DJ
Author(s): Beccero MA, Turon X, Uriz MJ
Author(s): Becerro MA, Thacker RW, Turon X, Uriz MJ, Paul VJ
Author(s): Muller WEG
Author(s): Lavrov D
Author(s): By Phil Myers
Author(s): Molinski TF, Dalisay DS, Lievens SL, Saludes JP
Author(s): Simmons TL, Andrianasolo E, McPhail K, Flatt P, Gerwick WH
Author(s): Gordaliza M
Author(s): Hallock YF, Cragg GM
Author(s): Hildebrand M, Waggoner LE, Lim GE, Sharp KH, Ridley CP, et al.
Author(s): Baker DD, Chu M, Oza U, Rajgarhia V
Author(s): Newman DJ, Cragg GM
Author(s): Newman DJ, Cragg GM
Author(s): Sagar S, Kaur M, Minneman KP
Author(s): Villa FA, Gerwick L
Author(s): Frota MJ, Silva RB, Mothes B, Henriques AT, Moreira JC
Author(s): Blunt JW, Copp BR, Keyzers RA, Munro MH, Prinsep MR
Author(s): Longeon A, Copp BR, Quévrain E, Roué M, Kientz B, et al.
Author(s): Utkina NK
Author(s): Li Z
Author(s): Sugiyama Y, Ito Y, Suzuki M, Hirota A
Author(s): Kim SK, Dewapriya P
Author(s): Berrué F, McCulloch MW, Boland P, Hart S, Harper MK, et al.
Author(s): Abraham I, El Sayed K, Chen ZS, Guo H
Author(s): Mayer AM, Glaser KB, Cuevas C, Jacobs RS, Kem W, et al.
Author(s): Crews P, Gewick WH, Schmitz FJ, France D, Bair KW, et al.
Author(s): Wang YQ, Miao ZH
Author(s): Bergmann W, Feeney RJ
Author(s): Proksch P, Edrada RA, Ebel R
Author(s): Schwartsmann G
Author(s): Feldman EJ, Lancet JE, Kolitz JE, Ritchie EK, Roboz GJ, et al.
Author(s): Essack M, Bajic VB, Archer JA
Author(s): Sipkema D, Osinga R, Schatton W, Mendola D, Tramper J, et al.
Author(s): Newman DJ, Cragg GM
Author(s): Halim H, Chunhacha P, Suwanborirux K, Chanvorachote P
Author(s): Guzii AG, Makarieva TN, Denisenko VA, Dmitrenok PS, Kuzmich AS, et al.
Author(s): Kondracki ML, Guyot M
Author(s): Kong D, Yamori T, Kobayashi M, Duan H
Author(s): Bai R, Cichacz ZA, Herald CL, Pettit GR, Hamel E
Author(s): Rothmeier AS, Schneiders UM, Wiedmann RM, Ischenko I, Bruns CJ, et al.
Author(s): Valeriote FA, Tenney K, Media J, Pietraszkiewicz H, Edelstein M, et al.
Author(s): Rabelo L, Monteiro N, Serquiz R, Santos P, Oliveira R, et al.
Author(s): Schumacher M, Cerella C, Eifes S, Chateauvieux S, Morceau F, et al.
Author(s): Shin BA, Kim YR, Lee IS, Sung CK, Hong J, et al.
Author(s): Zhao Q, Mansoor TA, Hong J, Lee CO, Im KS, et al.
Author(s): Gunasekera SP, Cranick S, Longley RE