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Origanum vulgare was used as an effective herbal for infertility treatment in traditional medicine. The present study compared the effects of the hydroalcoholic extract of the air branch of Origanum vulgare, LHRH-A_2, and17β-estradiol on the ultrastructure of oocyte and pituitary in immature Trichogaster trichopterus. For this purpose 60 pieces of Trichogaster trichopterus with average weight of 2.1±1gram were divided into 6 groups: saline, placebo, ethanol and 3 experimental groups (Origanum vulgare and 17β-estradiol at a dose of 50 mg/kg and LHRH-A₂ at a dose of 0.005 mg/kg) (each group 10 fish). Fish were injected intra-muscularly, one dose every other day and seven doses in total. Ultrastructure of oocyte and anterior pituitary in the three treatments were measured and compared with control treatments. The results showed that the size of oocytes follicle and the mean diameter of Golgi vesicles in Origanum vulgare treatment was higher than that in LHRH-A₂ treatment, but there were lesser than that in 17beta-estradiol treatment (p≤0.05). The results of the ultrastructural comparision of the anterior pituitary showed that in Origanum vulgare treatment the number of small cells increased and made a few large granules in gonadotroph cells. In fish treated with 17β-estradiol the number of large granules increased significantly, whereas in LHRH-A₂ treatment large granules were lysed and stimulation was complete. The present results suggested that the Origanum vulgare affected Trichogaster trichopterus fertility.

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Viviparity is an advanced reproducing process observed in certain bony fishes. Fish oocyte is protected by different coverings, the immediate one over oolemma being a non-cellular membrane known as Zona Radiata (ZR). ZR has shown variations in thickness, configuration and probably function at different fish oocyte and oocyte growth stages. In the present research work the ultrastructure of zona radiata around oocytes of guppy (Poecilia reticulata) has been studied by light and scanning electron microscopy methods concerning different oocyte growth stages. ZR was not observed at stages I and II. At stage III ZR was observed as a thin layer around the oocyte. It increased in thickness and complexity at stage IV (vitellogenesis) but showed different appearance and declined in thickness during the following stage. External surface characteristics, features of pore canals and probable function of ZR during oocyte development were also investigated.

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Aloe barbadensis is perennial, monocotyledonous, fleshy plant belongs to Aloaceae family. In this study, somoclonal variations of regenerated A. barbadensis plants were investigated. The plantlets of forth subculture transferred to the soil for further study. The genomic DNAs of 40 regenerated plantlets were extracted and genetic variations were studied using SPAR markers including RAPD and ISSR primers. The amounts of Aloe gel also were extracted from regenerated A. vera plants. Average percentage of polymorphism, Shannon index, Nei's genetic diversity and number of effective alleles based on RAPD data were higher than genetic parameters obtained from ISSR data. NJ cluster and STRUCTURE plot based on molecular markers grouped regenerated plants to distinct clusters. AMOVA analysis also showed a significant (P = 0.01) genetic distinction between studied groups. This result also confirmed differentiation of regenerated plants. The amount of Aloe gel in the four groups (based on clustering method) was compared by using analysis of variance (ANOVA). The results showed no significant (P = 0.746) differences between the amount of gel in four group. In total, our findings showed somaclonal variations on genomic level while no significant differences were observed in amount of gel among regenerated Aloe plantlets.
 

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Basic fibroblast growth factor (bFGF), also known as FGF-2, is a crucial member of the fibroblast growth factor family, involved in a variety of biological functions including cellular proliferation, wound healing, angiogenesis, intercellular signalling, and cell differentiation, In contemporary stem cell research, serum-free media enriched with various additives and growth factors are employed, and among these, bFGF being particularly significant. Despite its extensive potential applications, the clinical utilization of bFGF is limited due to its instability, especially in aqueous environment. Therefore, a thorough investigation of the protein's structural integrity and stability is essential. This study focuses on the expression, purification, and characterization of bFGF for structural and stability analysis through biophysical methods. Intrinsic fluorescence measurement indicated a structural alteration surrounding the tryptophan residue, while circular dichroism (CD) analysis showed a decrease in the protein’s secondary structure. The differential scanning calorimetry (DSC) used for stability analysis. Furthermore, the study aims to evaluate the biological activity of the protein in cellular context. For this purpose, gold nanoparticles were synthesized. The results from the Cell Migration Assay indicated that the proliferation of HT29 cells was enhanced following treatment with bFGF in conjunction with gold nanoparticles. Also, a MTT assay was conducted.