Sigmoid colon duplication with ectopic immature renal tissue in an adult:A case report

BACKGROUNDColonic duplication is a rare congenital anomaly. Many types of heterotopic tissuewere identified within the wall of duplication. However, studies of ectopicimmature renal tissue (EIRT) involving colon duplication in an adult have yet tobe reported.CASE SUMMARYA 23-year-old woman visited our hospital with symptoms of recurrent abdominalpain and chronic constipation. Image analysis via abdomino-pelvic computedtomography, Gastrografin contrast study, and colonoscopy showed a blind anddilated bowel loop filled with fecal material located on the mesenteric side of thesigmoid colon. We established a diagnosis of sigmoid colon duplication anddecided to perform a laparoscopic investigation. Segmental resection of thesigmoid colon with duplication was done. Microscopically, the duplicatedsegment showed all three layers of the bowel wall and EIRT in the wall of theduplication. The postoperative period was uneventful and the patient wasdischarged nine days after the surgery without complications. She has been doingwell 12 mo after the follow-up period.CONCLUSIONA comprehensive histopathologic examination for ectopic tissues or tumors ismandatory after resection of colon duplication.

A porous hydrogel scaffold mimicking the extracellular matrix with swim bladder derived collagen for renal tissue regeneration

As a worldwide public health issue, chronic kidney disease still lacks of effective therapeutic approaches due to the challenges in conventional organ transplantation and dialysis. Renal tissue engineering offers an advantageous therapeutic or regenerative option over typical donor organ. However, despite the great progress of decellularized extracellular matrix based scaffold for the renal regeneration, several safety concerns and complex composition still remain to be addressed. Herein, the extracellular matrix-mimicking hydrogel scaffolds were developed through covalent and physical cross-linking between swim bladder-derived natural collagen(COL) and anti-fibrosis chondroitin sulfate(CS) derivatives.The biomimetic hydrogels showed proper mechanical property, excellent thermal stability and high biocompatibility both in vitro and in vivo, by altering the mass ratio of COL and CS. When implanted in partially nephrectomized rat model, the 1 COL/2CS scaffold enable it recruit more native kidney cells, reduce the tubular damage, and even induce the regeneration of renal tubular-like tissue and restore renal metabolic function more effectively comparing with the pure 2COL and 2CS scaffold. These results suggest that the biomimetic scaffold is a promising functional platform for treating renal diseases.

Orthotopical transplantation of human renal carcinoma tissue into nude mice and the establishment of a high metastatic cell line MRCC

Objective To establish a SOI model of human renal carcinoma and a high metastatic cell subline. Methods A human renal cell line RCC-9863 has been established by inoculating a human renal tumor tissue into nude mice s. c.. When RCC-9863 passaged for 20 times, the tissue from the same xemotransplant tumor were used to construct SOI model. Cultured the metastatic tissue in vitro, the tumor cell suspension was then injected orthotopically, The metastatic tissue obtained underwent the same procedure again. At last, the metastatic tumor was cultured in vitro and cloned. Results 15 days later, a tumor mass sized 1. 7 cm × 0. 6 cm in the nude mouse’s renal parenchyma was grown which lobulated, rude, and with multiply blood vessels and 55 days later later the mouse became moribund and metastases in the lungs were formed. The transplanted renal tumor in the SOI model grew fast and invasively and metastasized to lungs, lymphatic node and liver. A subline, MRCC, with metastatic ability to the lung was selected.

Assessment of Nephro-, Hepato-, and Sex-Dependent Toxicity of Carmoisine Exposure in Albino Rats

Aim: To evaluate chronic exposure of carmoisine at ADI doses on some hepatocellular and renal parameters of male and female albino rats as well as to determine sex-dependent toxicity. Study Design: The study involves treatment for 30, 60, and 90 days. Each phase consists of 40 rats, divided into treatment and control groups. The treated groups were orally administered with 4.0 mg/kg of carmoisine daily for the periods of 30, 60, and 90 days. Methodology: At the end of the treatment, the rats were allowed to fast for 18 hours followed by the collection of 5 ml of whole blood specimens by means of cardiac puncture into Lithium Heparin bottles and fluoride oxalate bottles (for glucose only). Plasma obtained was analyzed for glucose (GLU), AST, ALT, ALP, creatinine (CRT), and urea. Hepatic and Renal tissues collected were fixed in 10% formol saline and later examined histologically using H&E stain. Statistical data analysis was done using GraphPad Prism version 9.02. Results: Glucose indicated significant increases after 30, 60, and 90 days of chronic treatment at ADI doses. Urea, Creatinine, AST, ALT and ALP showed significantly higher values after 60 and 90 days of treatment (except creatinine in male rats and ALP in female rats after 60 and 90 days respectively). Hepatic distortions, vacuolation, compression of central vein were seen in the liver section while distortion of proximal and distal tubules, and inflammation of the glomerulus were observed in the renal tissue of the treated rats. Conclusion: The administration of camoisine over a period of 30 days at ADI dose did not indicate hepatocellullar and renal derangements as well histological distortions in liver, and kidneys. However, after 60 and 90 days, mild hepatocellular, and renal derangements were seen. No sex-dependent toxicity was observed.

Altered nuclear factor-kappaB inducing kinase expression in insulin-resistant mice

Background Insulin resistance is an underlying feature of both type 2 diabetes and metabolic syndrome. Currently, it is unclear whether nuclear factor （NF）-KB inducing kinase （NIK） plays a role in the development of insulin resistance. The present in vivo study investigated the roles of NIK and IKB kinase a （IKKa） in obesity-induced insulin resistance using animal models. Methods NIK expression was evaluated by Western blotting in male Lepob mice and C57BL/6J mice fed a high-fat diet （HFD） （45% fat）. After metformin and sulfasalazine treatment, NIK expression was investigated during the improvement of insulin resistance. Results NIK was increased by about 1-fold in the renal tissues of Lepab mice and C57BL/6J mice fed a HFD for 12 weeks. After 1 and 3 weeks of high-fat feeding, we observed an almost 50% decrease in NIK and IKKa expression in the liver and renal tissues of C57BL/6J mice. NIK expression was significantly lower in the liver and renal tissues of HFD-fed mice that were treated with insulin sensitizers, metformin and sulfasalazine. However, IKKa expression was increased after metformin treatment in both tissues. Conclusion These results suggest a possible role of NIK in the liver and renal tissues of insulin-resistant mice.