RESUMEN
Prenatal supplementation of high-value PUFA (HVPUFA) is essential for adequate brain development in infants. As marine microalgal derived omega-3 fatty acids are considered an alternative source of fish oil, their neuroprotective role on monosodium glutamate (MSG)-induced neurotoxicity, bioavailability, and disease prevention in first-generation (F1) animals need to be explored at molecular level. This study tested the long term supplementation of microalgal derived ω-3 PUFAs from parent rats to its offspring rats and studied the neuroprotective role in monosodium glutamate (MSG)-induced neurotoxicity in F1 rats. The parent animals were divided into three groups: control, microalgal-administered group (5.7 mg of EPA and 1.4 mg of DHA/kg BW from Isochrysis sp.), and fish oil-administered group (4.2 mg of EPA and 2.9 mg of DHA/kg BW derived from fish oil) (FG) and continued up to F1 generation. The F1 male rats from respective parents were separated for disease induction: group I animals (control) were administered with 500 µl of Milli-q water alone and group II (disease control), III (Microalga), and IV (fish oil) animals were administered with 2 g/kg bodyweight of MSG for 10 alternative days. Microalga-treated F1 rats showed significant HDL (43 mg/dl) levels when compared to their experimental groups. Brain tissues of microalga-treated F1 rats (MG) showed higher concentration of DHA (10.1 mg/100 mg tissue) and ARA (18.7 mg/100 mg tissue) levels and significant reduction of MDA (30 nM mg protein) levels. Furthermore, MSG induced neurotoxicity was ameliorated through the activation of CREB and BDNF genes The mRNA expressions of CREB and BDNF were 1.5-fold higher and NMDA levels were 2.0-fold higher in treated groups compared to disease control group. However, the expressions of antioxidant genes (SOD, catalase, and GPX) and apoptotic genes (Bcl-2 and Caspase-3) were significantly reduced in MG treated F1 rats when compared to disease control rats. Histopathological results also showed minimal focal damage in the tissues of MG F1 rats. Prenatal and continuous supply of microalgal biomass improves brain DHA and greatly reduced the consequences of MSG neurotoxicity in F1 rats.
Asunto(s)
Haptophyta , Glutamato de Sodio , Animales , Biomasa , Suplementos Dietéticos , Masculino , Ratas , Ratas Wistar , Glutamato de Sodio/toxicidadRESUMEN
AIM: This study investigated the effect of several metabolic enhancers on the expression of fatty acid biosynthetic genes and their influence on the production of high-value PUFA in the marine microalgae Isochrysis sp., CASA CC 101. METHODS AND RESULTS: The effect of the presence of iron (Fe), nicotinic acid (NIC), methyl jasmonate (MJ) and thidiazuron (TDZ) on the expression of the fatty acid desaturase genes Δ6Des, Δ5Des and Δ4Des was studied in cultures of the marine microalga Isochrysis sp., CASA CC 101. The production of high-value PUFA like γ-linolenic acid (GLA), eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) was correlated with these gene expressions. The results showed that MJ, Fe and TDZ significantly increased the lipid content than the control. MJ specifically up-regulated ∆6Des gene expression and thereby increased GLA production. Whereas Fe specifically increased ∆5Des gene expression and thereby increased EPA production. However, Fe and TDZ-treated cells effectively upregulated the expression of ∆4Des and increased the production of DHA when compared with control cells. CONCLUSIONS: Our findings suggest that addition of Fe and MJ in the culture medium triggers the expression of PUFA biosynthetic genes, especially ∆6Des and ∆4Des, in marine microalga Isochrysis sp., CASA CC 101 their presence resulted in increased production of the PUFAs GLA, EPA and DHA. SIGNIFICANCE AND IMPACT OF THE STUDY: This study shows that the addition of Fe and MJ to the culture media of Isochrysis sp., CASA CC 101 results in up-regulation of its genes Δ4Des, Δ6Des and Δ5Des, and improves the production of PUFA. Therefore, the addition of Fe and MJ to the culture medium is useful to increase the production of high-value PUFA in Isochrysis sp., CASA CC 101 and also to the other micro algal species.
Asunto(s)
Haptophyta , Microalgas , Acetatos , Ciclopentanos , Ácidos Docosahexaenoicos , Ácido Eicosapentaenoico , Ácido Graso Desaturasas/genética , Ácido Graso Desaturasas/metabolismo , Haptophyta/genética , Hierro/metabolismo , Microalgas/genética , Microalgas/metabolismo , OxilipinasRESUMEN
Bimetallic or alloy nanoparticles (NPs) have improved properties compared to their monometallic forms. Microalgae being rich in biocompatible reductants and being ecofriendly are potential sources to synthesize fuctionalized NPs. In this study, biosynthesis of silver, gold, and bimetallic NPs was carried out via bioreduction using aqueous extract of algal isolate Chlorella acidophile, inhabitant of non-arable land. C. acidophile is known to contain highly bioactive functional moieties, which can serve as nanobiofactories for metallic NPs. Various characterization techniques viz, UV-visible spectrophotometer, X-ray diffraction analysis, X-ray photo-electron spectroscopy, and Raman spectroscopy were employed to determine their composition, structure, and crystal phase. The monometallic and bimetallic particles were found to be crystalline state and generally in a spherical shape. Their size ranged from 5 to 45 nm and the corresponding FTIR spectra indicated that the specific organic functional groups from algal extract were involved in the bio-reduction. Furthermore, the core-shell in the case of Au-Ag NPs was formed due to the simultaneous reduction of gold and silver ions. An enhanced and more pronounced Raman spectra of Au-Ag NP compared to individual Au NP indicated the improved properties of bimetallic NPs, the latter having been of immense potential to be used as sensors in industries.