Enhancing Rahmani Ram Semen Cryosurvival Through Oral Moringa Oil and Microencapsulation: In Vivo and In Silico
Wael A Khalil1, Alaa M A Gad1, Aya A Ismail1
1Department of Animal Production, Faculty of Agriculture, Mansoura University, Mansoura, Egypt.
Abstract:
Cryopreservation of ram semen is challenged by the high polyunsaturated fatty acid content in spermatozoa, which leads to increased oxidative stress and cellular damage. This study explored the potential of orally administered moringa oil (MO) or its microencapsulated form (MON) to protect ram spermatozoa during cryopreservation by assessing their effects on semen quality, antioxidant capacity, apoptosis, seminal metabolic enzyme activity, as well as molecular docking study. Fifteen Rahmani rams were randomly split into three groups (n = 5 per group) and fed a basal diet. The control group (CON) received 1 mL of distilled water orally, while the second and third groups received 2 mL of MO or 1 mL of MON, respectively, daily for 4 months. Semen samples were collected bi-weekly using an artificial vagina, pooled, extended and cryopreserved following standard protocols. Results demonstrated significantly higher (p < 0.05) post-thaw sperm viability, progressive motility and membrane integrity in the MO group compared to other groups after equilibration (at 5°C for 4 h), post-thawed ram semen (at 37°C for 30 s) or incubated at 37°C and 5% CO2 for 2 h. Regarding apoptotic sperm, the orally administered MO group had a significantly greater number of viable spermatozoa (p < 0.001) than the other groups. Although all treated groups had a lower percentage of early apoptosis than the control, MON administration resulted in a significant increase in the percentages of necrotic sperm compared to the MO group (p < 0.05). The TAC was highest and MDA was lowest (p < 0.05) in the MO group. Molecular docking analysis revealed the binding energies (kcal/mol) of bioactive compounds from MO including apigenin, ferulic acid and naringenin with three target proteins: ADAM17 (-4.47, -4.49 and -4.88, respectively), DNase1 (-4.42, -3.47 and -4.46, respectively) and SHBG (-6.38, -4.70 and -6.43, respectively). These findings indicate that orally administering MO has a more pronounced positive effect on Rahmani ram semen quality, apoptosis, and antioxidant status following cryopreservation compared to its microencapsulated form.
Insights
Oral administration of moringa oil (MO) significantly improved ram sperm quality and viability after cryopreservation. MO offered better protection against oxidative stress and apoptosis compared to its microencapsulated form (MON).
Area of Science:
- Veterinary Science
- Reproductive Biology
- Biochemistry
Background:
- Cryopreservation of ram semen is hindered by high polyunsaturated fatty acid content, leading to oxidative stress and cellular damage.
- Moringa oil (MO) and its microencapsulated form (MON) were investigated for their potential to mitigate cryodamage in ram spermatozoa.
Purpose of the Study:
- To evaluate the efficacy of orally administered MO and MON in protecting ram spermatozoa during cryopreservation.
- To assess the impact of MO and MON on semen quality, antioxidant capacity, apoptosis, and seminal metabolic enzyme activity.
Main Methods:
- Rahmani rams were divided into three groups: control (distilled water), MO, and MON, receiving daily oral doses for 4 months.
- Semen was collected, cryopreserved, and evaluated for post-thaw sperm viability, motility, membrane integrity, apoptosis, total antioxidant capacity (TAC), and malondialdehyde (MDA) levels.
- Molecular docking studies were performed to analyze the binding of MO's bioactive compounds with target proteins.
Main Results:
- The MO group exhibited significantly higher post-thaw sperm viability, progressive motility, and membrane integrity compared to control and MON groups.
- MO administration resulted in a significantly greater number of viable spermatozoa and lower levels of early apoptosis.
- The MO group showed the highest TAC and lowest MDA levels, indicating superior antioxidant protection.
Conclusions:
- Oral administration of moringa oil (MO) significantly enhances the cryopreservation of ram semen by improving sperm quality and antioxidant status.
- MO provides superior protection to ram spermatozoa during cryopreservation compared to its microencapsulated form (MON).
- Bioactive compounds in MO, identified through molecular docking, contribute to its protective effects against cryodamage.
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