Anatomical with Histological structures of the mammary gland in small ruminants [Ewe and She goat] as well as the pattern of intra mammary duct system using mammography were studies to obtain more details information about the mammary glands of small ruminants for its value in production of milk.

The present study was conducted on (40) white mice of approximately the same age (4-6 weeks) and body weight (23-25 gm) for the aim of observing the histopathological changes for male and female reproductive organs due to prolonged treatment (6 months) with anticancer chemotherapeutic agent namely methotrexate. Forty mice were divided into 4 groups (10 mice of each group 5 mice per sex). The first group (low or therapeutic dose group) was received 0.15 mg/kg B.W. The second group (intermediate dose group ) received 0.3 mg/kg B.W. The third group ( toxic dose group ) received 0.45 mg/kg B.W. the fourth group was a control group; it received 0.2 ml buffered physiological saline. All these groups injected intramuscularly, once weekly for 6 months. The results showed that methotrexate can cause suppression of spermatogenesis. In female, methotrexate can cause obvious pathological changes in uteri and ovaries such as reduced endometrial glands and ovarian follicles respectively

Sildenafil citrate (Viagra) is an oral medication used to treat male impotence by the inhibition of phosphodiesterase-5 in the corpus cavernosum and subsequent facilitation of penile erection. The side effects of sildenafil citrate have been reported. The present study was designed to investigate the effect of long term administration of sildenafil citrate on some characteristics (sperm count, sperm malformations) and testis architecture of male rats. The results indicated that the oral administration of 50 mg and 100 mg of suldinafil citrate (Viagra) for 8 weeks caused a significant decreased and a significant increased in sperm count and sperm malformations respectively. The results were showed the histopathological changes in testis of male rats treated with 50 mg and 100 mg sildenafil citrate..

The protoscolices of Echinococcus granulosus in vitro compared with the two drugs Tinidazole and Praziquantel using the concentrations (5 , 10 , 15 , 20) % of the plant extracts and (1.25 , 1.8 , 2.5) % for Tinidazole and (0.1 , 0.15 , 0.2) % for Praziquantel respectively. The study shows that the aqueous extract at 20% have showen highest protoscolicidal activity. All the protoscolices were killed in the first day after treatment. While the concentration 5% shows the lowest activity in killing the protoscolices which was in the 6th day , while the time of killing protoscolices was in the 3rd day and 2nd day at the concentration (10 , 15)% respectively. There is no significant differences between aqueous and alcoholic extract of Cyperus longous P< 0.01 , so aqueous extract used in our study because of its lower price and its safety. Tinidazole and Praziquantel have showen the great activity on killing the protoscolices in the 30 & 60 minutes at (2.5 , 0.2) % respectively. The preservative solution (Hankُ s solution). Keep the protoscolices viable 59% to 21 days.

In this study ,the antibacterial activity of aqueous and purified pigment extracts of Ipomoea purpurea were tested against reference strains of Staphylococcus aureus and Esherichia coli . The preliminary qualitative tests showed that the two extracts have flavonoids, carbohydrates and glycosides ,While alkaloids found only in the aqueous extract ,Thin Layer Chromatography (TLC) showed the presence of anthocyanin pigment , both extracts gave a clear activity against the tested strains with a minimal Inhibitory Concentration reached to 25mg/ml

The present study was carried out to determine the effect of super benzene inhalathion and its metabolites on haemopoietic tissues(spleen and bone marrow) on experimental rats.Animals were exposed via inhalation to concentrations of (5 and 10) ppm super benzene for 2 hour/day, 5 days /week for 3 months.Histological studies revealed that spleen of the exposed animals to super benzene, were exposed to 5 ppm showed white pulp atrophy and absence of megakaryocytes in red pulp with blood vessels congestion.In 10 ppm showed increased of extramedulary haemopoiesis, acute splenitis and fibrosis as well as showed aggregation of lymphocytes in lymph node, thickness with centeral artery wall also inflammation of inflammatory cells inside centeral artery and vasodilatation in centeral artery in asplenic nodule.While the bone marrow related to the animals exposed to 5 and 10 ppm showed reduced in haemapoietic tissue which partly replaced by adipose tissue.

To determine the suitability and estimate the sensitivity of an immunohistochemical (IHC) test for disease-associated prion protein (PrP(Sc)) in biopsy specimens of rectoanal mucosa-associated lymphoid tissue (RAMALT) for diagnosis of scrapie in sheep. 762 sheep at high risk for having scrapie and indemnified by the National Scrapie Eradication Program. The IHC test for PrP(Sc) was applied to 2 RAMALT and 2 third-eyelid biopsy specimens and a postmortem RAMALT specimen from each sheep. Results were compared with those of a reference test in which results for tissues from obex and retropharyngeal lymph nodes, tonsil, or both were considered in parallel. The reference test identified 139 sheep as having scrapie. Biopsy-related complications occurred in 3 sheep. Sensitivity of the IHC test in RAMALT ranged from 85.3% to 89.4%, depending on the anatomic location from which RAMALT was obtained. Results for the test applied to 1 RAMALT specimen were similar to results interpreted in parallel for 2 third-eyelid specimens (sensitivity, 87.0%). The proportion of inconclusive test results attributable to insufficient lymphoid follicles in biopsy specimens was lower when considering results for 2 RAMALT specimens in parallel (10.1%) than when considering results for 2 third-eyelid specimens in parallel (23.7%). Specimens of RAMALT that were inappropriately collected from an area caudal to the rectoanal interface yielded a high proportion of inconclusive results (33.3% to 50.0%). The IHC test for PrP(Sc) in RAMALT was an effective means of detecting subclinical scrapie in live, high-risk sheep.

The ubiquitin-proteasome mediated protein degradation pathway plays an important role in regulating both cell proliferation and cell death. Proteasome inhibitors are well known to induce apoptosis in various human cancer cell lines. We investigated the effect of combined treatment with proteasome inhibitor and TRAIL, and a possible mechanism of the enhancing apoptosis by the both treatment, on TRAIL-resistant non-small cell lung cancer. A549 cells were exposed to the N-Acetyl-Leu-Leu-Norleu-al(ALLN) as a proteasome inhibitor and then treated with recombinant TRAIL protein. In A 549 cells under proteasome inhibition conditions by pretreatment with ALLN, TRAIL treatment significantly decreased cell vibility compared to that ALLN and TRAIL alone treatment. Also, the both treatment induced cell damage through DNA fragmentation and p53 expression. In addition, the combined treatment of both markedly increased caspase-8 activation, especially the exposure for 2h, and Bax expression and induced the dissipation of mitochondrial transmembrane potential in A549 cells. Taken together, these findings showed that proteasome inhibition by ALLN enhanced TRAIL-induced apoptosis via DNA degradation by activated P53 and mitochondrial transmembrane potential loss by caspase-8 activation and bax expression. Therefore, our results suggest that proteasome inhibitor may be used a very effectively chemotherapeutic agent for the tumor treatment, especeally TRAIL-resistant tumor cell.

The effect of Bu-Zhong-Yi-Qi-Tan (BZYQT) on the changes of ultraviolet (UV) light B radiation-induced apoptotic sunburn cell (SBC) and epidermal ATPase-positive dendritic cell (DC) in SKH1-hr or ICR mouse were investigated. The mice were treated with UVB (200 mj/㎠) and were sacrificed 24 h later. BZYQT (50 mg/kg of body weight) or vehicle (saline) was given i.p. at 36 and 12 h before irradiation, and 30 min after irradiation or BZYQT cream (0.2%) or cream base (vehicle) was topically treated at 24 h and 15 min before irradiation, and immediately after irradiation. The skin of SKH1-hr mouse prepared from the back of untreated mice exhibited about 0.3 SBC/cm length of epidermis, and 24 h after UV irradiation, the applied areas show an increased number of SBCs. But the frequency of UVB-induced SBC formation was reduced by intraperitoneal injection of BZYQT extract (p less than 0.01). The numbers of DC in normal ICR mouse were 628.00 ± 51.56 or 663.20 ± 62.58 per ㎟ of ear epidermis. By 1 day after UVB treatment, the number of ATPase-positive cells/㎟ were decreased by 39.0% or 27.1% in i.p. or topical application group with vehicle. Treatment of BZYQT was associated with increase of 33.9% in i.p. group (p less than 0.05) or 2.7% in topical application group in the number of ATPase positive cells compared with the irradiation control group. The results presented herein that BZYQT administration could reduce the extent of skin damages produced by UVB.

Transmission of avian viruses both bird-to-bird and from birds to non-avian species is a major health concern. Newcastle disease virus (NDV) is an economically important avian virus that poses substantial risks to the poultry industry. Rapid and sensitive diagnostic methods, such as the enzyme-linked immunosorbent assay (ELISA), are required to track such infections. To develop an ELISA for detecting anti-NDV antibody in avian sera, the nucleocapsid protein (NCP) gene of the NDV La Sota strain was cloned and expressed in Escherichia coli and the 513-amino acid recombinant NCP was purified by Ni-NTA affinity chromatography. To evaluate its ability to replace NDV whole virus antigen as a coating antigen, NCP-coated and whole NDV-coated ELISAs were tested and compared using a panel of NDV positive antisera from chickens. Results using purified NCP were highly correlated with those obtained using whole NDV (r=0.927), demonstrating that recombinant NCP expressed in Escherichia coli is a suitable substitute antigen for whole NDV in a diagnostic ELISA.