Nowadays, pig has been chosen as the potential source of organs and cells for human to overcome a sever shortage of human material for clinical transplantation especially in the last 10 years by use of genetically modified swine. Consequently, the present study was conducted to give detailed information about the distribution of the blood vessels and bile ducts and their topographic relations, which may give a useful base for the hepatic segmentation in this animal aiming to provide a correct base for surgical procedures and liver transplantation. � The present study was conducted on 33 livers of pigs. Dissection, casting and radio-opaque techniques have been applied to show the different ramifications of the portal vein, hepatic artery and bile duct systems as well as their topographic relations with proposals of hepatic segmentation. The results revealed that, the caudate, right lateral and right medial lobes were supplied by R. dorsalis dexter and R. ventralis dexter of the portal vein in addition to R. dexter of the hepatic artery and right hepatic duct. The quadrate, left medial and left lateral lobes were supplied by the R. sinister of the portal vein and hepatic artery and left hepatic duct. � The liver of the pig could be divided into two independent segments; right and left. These two segments were separated by a segmental plane passed from the esophageal notch dorsally to the fossa of the gall bladder ventrally.

Morphometry of the spinal cord of the rabbit Farag et al.

Internal anatomy of the common carp Farag et al.

Background The testes are highly susceptible to the adverse effects of chemotherapy and radiation at all stages of life. Exposure to these threats mainly occurs during cancer treatment and as an occupational hazard in radiation centers. The present study investigated the regenerative ability of adipose-derived mesenchymal stem cells (ADMSCs) against the adverse effects of cisplatin on the structure and function of the testes. Methods New Zealand white rabbits (N = 15) were divided into three groups of five: a negative control group (no treatment), a cisplatin group (single dose of cisplatin into each testis followed three days later by a PBS injection), and a cisplatin + ADMSCs group (cisplatin injection followed three days later by an ADMSC injection). On day 45 post-treatment, serum testosterone levels were evaluated, and the testes and epididymis were collected for histology, oxidative stress examination, and epididymal sperm analysis. Results Cisplatin caused damage to the testicular tissue and decreased serum testosterone levels, epididymal sperm counts, and oxidants. An antioxidant imbalance was detected due to increasing malondialdehyde (MDA) and reduced glutathione (GSH) levels in testicular tissue. The ADMSC-treated group displayed a moderate epididymal sperm count, adequate antioxidant protection, suitable hormone levels, and enhanced testicular tissue morphology. Conclusions ADMSCs treatment repaired damaged testicular tissue, enhanced biochemical parameters, and modified pathological changes caused by cisplatin.

Infertility is a serious medical, economic, and psychological problem in the society. Male factor infertility, due to defective spermatogenesis as a result of a failure in germ cell proliferation and differentiation, appears to be the cause of 25–50% of infertility cases. According to several surveys, testicular degeneration can be caused by a variety of physical, chemical, and microbial causes. A stem cell is a non-specialized cell which is characterized by self-renewal by mitotic cell division and able to differentiate to specialized cells for the various tissues of the body. The data were obtained and analyzed from different databases (PubMed, Google Scholar, Egyptian Knowledge Bank, Elsevier, Medline, Embase, ProQuest, and BMC). This review discusses the causes, symptoms, and grades of testicular degeneration and the use of different types of stem cells in regeneration. And its conclusion based on previous researches and trials, MSCs are considered effective therapy for testicular degeneration.