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1.
Br J Nutr ; 126(4): 510-517, 2021 08 28.
Article in English | MEDLINE | ID: mdl-33143765

ABSTRACT

To evaluate the impacts of guanidinoacetic acid (GAA) and coated folic acid (CFA) on growth performance, nutrient digestion and hepatic gene expression, fifty-two Angus bulls were assigned to four groups in a 2 × 2 factor experimental design. The CFA of 0 or 6 mg/kg dietary DM folic acid was supplemented in diets with GAA of 0 (GAA-) or 0·6 g/kg DM (GAA+), respectively. Average daily gain (ADG), feed efficiency and hepatic creatine concentration increased with GAA or CFA addition, and the increased magnitude of these parameters was greater for addition of CFA in GAA- diets than in GAA+ diets. Blood creatine concentration increased with GAA or CFA addition, and greater increase was observed when CFA was supplemented in GAA+ diets than in GAA- diets. DM intake was unchanged, but rumen total SCFA concentration and digestibilities of DM, crude protein, neutral-detergent fibre and acid-detergent fibre increased with the addition of GAA or CFA. Acetate:propionate ratio was unaffected by GAA, but increased for CFA addition. Increase in blood concentrations of albumin, total protein and insulin-like growth factor-1 (IGF-1) was observed for GAA or CFA addition. Blood folate concentration was decreased by GAA, but increased with CFA addition. Hepatic expressions of IGF-1, phosphoinositide 3-kinase, protein kinase B, mammalian target of rapamycin and ribosomal protein S6 kinase increased with GAA or CFA addition. Results indicated that the combined supplementation of GAA and CFA could not cause ADG increase more when compared with GAA or CFA addition alone.


Subject(s)
Animal Feed , Cattle/growth & development , Folic Acid/administration & dosage , Glycine/analogs & derivatives , Animal Feed/analysis , Animal Nutritional Physiological Phenomena , Animals , Creatine , Detergents , Diet/veterinary , Dietary Supplements , Digestion , Gene Expression , Glycine/administration & dosage , Insulin-Like Growth Factor I , Liver , Male , Nutrients , Phosphatidylinositol 3-Kinases , Rumen
2.
Clin Exp Dermatol ; 38(4): 344-51, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23551214

ABSTRACT

BACKGROUND: Various laser and light sources are been used increasingly in cosmetic dermatology. AIM: To evaluate the efficacy and safety of combination intense pulsed light (IPL) and fractional CO2 laser in treating patients with acne with both inflammatory and scarring lesions. METHODS: In total, 37 Chinese patients with acne with facial inflammatory and scar lesions were treated. Successive sessions of 4-6 IPL treatments followed by 2 sessions of fractional CO2 laser treatments were applied. Effectiveness was determined by the dermatologist's evaluation, patient self-assessment, and devices that measure skin colour, sebum secretion and skin hydration. RESULTS: IPL treatments significantly reduced the inflammatory lesion score and the atrophic scar score compared with baseline. Subsequent fractional CO2 laser treatments further decreased the atrophic scar score. Both scores remained low when patients were followed up at 6 months. Around 90% of the patients experienced significant or moderate overall improvement, and almost 80% patients rated their results as 'excellent' or 'good'. The melanin index (MI), erythema index (EI) and skin sebum level all significantly decreased after IPL treatments, and the EI and sebum level were still low when assessed at the 3-month follow-up, although the MI had increased again. The adverse effects (AEs) of both treatments were transient and bearable. CONCLUSIONS: IPL in combination with fractional CO2 laser was effective in treating patients with acne with both inflammatory lesions and atrophic scars, and the AEs were acceptable.


Subject(s)
Acne Vulgaris/therapy , Cicatrix/therapy , Inflammation/therapy , Intense Pulsed Light Therapy , Lasers, Gas/therapeutic use , Acne Vulgaris/complications , Adult , Asian People , China , Cicatrix/etiology , Female , Humans , Inflammation/etiology , Low-Level Light Therapy , Male , Patient Satisfaction , Young Adult
3.
Nutr Metab Cardiovasc Dis ; 22(6): 463-70, 2012 Jun.
Article in English | MEDLINE | ID: mdl-21310599

ABSTRACT

BACKGROUND AND AIM: The effect of soy isoflavones on blood pressure is controversial. The objective of this study was to evaluate the effect of dietary soy isoflavones on blood pressure. METHODS AND RESULTS: Trials were searched in PubMed, the Cochrane Library, Embase and references cited in related reviews and studies. A total of eleven trials were reviewed. Meta-analysis results showed a mean decrease of 2.5 mm Hg (95% CIs, - 5.35 to 0.34 mm Hg; P = 0.08) for systolic blood pressure and 1.5 mm Hg (95% CIs, - 3.09 to 0.17 mm Hg; P = 0.08) for diastolic blood pressure in the soy isoflavones-treated group compared to placebo. Meta-regression and subgroup analyses indicated that blood pressure status was a significant predictor of heterogeneity for the effect of soy isoflavones on blood pressure. Subgroup analysis of hypertensive subjects revealed that a greater blood pressure reduction was identified in the soy isoflavone-treated group compared to placebo (5 trials; SBP: - 5.94, 95% CIs [- 10.55, - 1.34] mm Hg, P = 0.01; DBP: - 3.35, 95% CIs [- 6.52, - 0.19] mm Hg, P = 0.04). In contrast, treatment with soy isoflavones did not lead to a significant reduction in blood pressure in normotensive subjects (6 trials; SBP: 0.29, 95% CIs [- 2.39, 2.97] mm Hg, P = 0.83; DBP: - 0.43, 95% CIs [- 1.66, 0.81] mm Hg, P = 0.50). CONCLUSION: Soy isoflavones had an effect of lowering blood pressure in hypertensive subjects, but not in normotensive subjects. Larger trials need to be carried out to confirm the present findings.


Subject(s)
Blood Pressure/drug effects , Glycine max/chemistry , Isoflavones/pharmacology , Plant Extracts/pharmacology , Databases, Factual , Energy Intake , Humans , Randomized Controlled Trials as Topic
4.
Eur J Pediatr Surg ; 20(6): 375-8, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20954107

ABSTRACT

INTRODUCTION: The diagnosis of long segment Hirschsprung's disease (LSHD) is frequently delayed. Our purpose was to: 1) summarize contrast enema (CE) findings in patients with LSHD, and 2) evaluate the utility of CE by comparing LSHD patients managed with/without pre-biopsy CE. METHODS: All LSHD cases (transition zone [TZ] proximal to the splenic flexure) treated between 1984 and 2009 were stratified according to whether a pre-biopsy CE was done (Group 1) or not (Group 2). CE were reviewed by a single pediatric radiologist, and the original reports were categorized as "helpful", "inconclusive" or "misleading". Group comparisons included elapsed days from admission to diagnostic rectal biopsy/first operation and initial hospitalization length of stay (LOS). RESULTS: 29 patients (16 in Group 1; 13 in Group 2) were identified. CE review revealed TZ in 7/16 (44%); and of these, 6 (86%) underestimated the actual aganglionic segment length. 6/16 (38%) original CE reports were "misleading". Overall, Group 1 patients experienced a significant delay in time to biopsy (p=0.047), first operation (p=0.005), and showed a trend towards prolonged LOS. CONCLUSIONS: Pre-biopsy CE offers little to the diagnosis of LSHD and may contribute to diagnosis/treatment delays. Even if a TZ is recognized in biopsy proven HD, the predicted aganglionic segment length should not guide the operative planning.


Subject(s)
Colon/pathology , Hirschsprung Disease/diagnostic imaging , Hirschsprung Disease/pathology , Rectum/pathology , Barium Sulfate , Biopsy , Contrast Media , Enema , Humans , Radiography , Retrospective Studies
5.
Xenobiotica ; 39(11): 850-61, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19845436

ABSTRACT

GDC-0449 (2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(methylsulfonyl)benzamide) is a potent, selective Hedgehog (Hh) signalling pathway inhibitor being developed for the treatment of various cancers. The in vivo clearance of GDC-0449 was estimated to be 23.0, 4.65, 0.338, and 19.3 ml min(-1) kg(-1) in mouse, rat, dog and monkeys, respectively. The volume of distribution ranged from 0.490 in rats to 1.68 l kg(-1) in mice. Oral bioavailability ranged from 13% in monkeys to 53% in dogs. Predicted human clearance using allometry was 0.096-0.649 ml min(-1) kg(-1) and the predicted volume of distribution was 0.766 l kg(-1). Protein binding was extensive with an unbound fraction less than or equal to 6%, and the blood-to-plasma partition ratio ranged from 0.6 to 0.8 in all species tested. GDC-0449 was metabolically stable in mouse, rat, dog and human hepatocytes and had a more rapid turnover in monkey hepatocytes. Proposed metabolites from exploratory metabolite identification in vitro (rat, dog and human liver microsomes) and in vivo (dog and rat urine) include three primary oxidative metabolites (M1-M3) and three sequential glucuronides (M4-M6). Oxidative metabolites identified in microsomes M1 and M3 were formed primarily by P4503A4/5 (M1) and P4502C9 (M3). GDC-0449 was not a potent inhibitor of P4501A2, P4502B6, P4502D6, and P4503A4/5 with IC50 estimates greater than 20 microM. K(i)'s estimated for P4502C8, P4502C9 and P4502C19 and were 6.0, 5.4 and 24 microM, respectively. An evaluation with Simcyp suggests that GDC-0449 has a low potential of inhibiting P4502C8 and P4502C9. Furthermore, GDC-0449 (15 microM) was not a potent P-glycoprotein/ABCB1 inhibitor in MDR1-MDCK cells. Overall, GDC-0449 has an attractive preclinical profile and is currently in Phase II clinical trials.


Subject(s)
Anilides/pharmacokinetics , Antineoplastic Agents/pharmacokinetics , Hedgehog Proteins/antagonists & inhibitors , Microsomes, Liver/metabolism , Pyridines/pharmacokinetics , Administration, Oral , Animals , Biological Availability , Cytochrome P-450 Enzyme System/metabolism , Dogs , Drug Evaluation, Preclinical , Hepatocytes/drug effects , Hepatocytes/enzymology , Humans , Injections, Intravenous , Macaca fascicularis , Metabolic Clearance Rate , Mice , Microsomes, Liver/drug effects , Rabbits , Rats , Rats, Sprague-Dawley
6.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 14(10): 595-7, 1994 Oct.
Article in Chinese | MEDLINE | ID: mdl-7719091

ABSTRACT

47 cases of adhesive intestinal obstruction after decompression operation were treated with intraperitoneal perfusion of compound injection of Salvia Miltiorrhizam intraperitoneally before closing the abdominal cavity and Dachengqi decoction oral given post-operatively. Follow up study for 2-9 years showed the effective rate was 100% except one case died of other unrelevant disease. Another 38 cases of the same disease and same operation procedure were selected as the control group, which were given antibiotics intraperitoneally before closing the abdominal cavity. The effective rate was 73.38%. The result in the therapeutic group was significantly better than that in the control group (P < 0.01).


Subject(s)
Drugs, Chinese Herbal/administration & dosage , Intestinal Obstruction/drug therapy , Adolescent , Adult , Aged , Amikacin/administration & dosage , Combined Modality Therapy , Female , Follow-Up Studies , Humans , Infusions, Parenteral , Intestinal Obstruction/surgery , Intraoperative Period , Male , Middle Aged , Plant Extracts , Salvia miltiorrhiza , Tissue Adhesions
7.
Zhong Xi Yi Jie He Za Zhi ; 10(12): 717-9, 707, 1990 Dec.
Article in Chinese | MEDLINE | ID: mdl-2292116

ABSTRACT

This study observed the effect of chemotherapy combined with Chinese herbs and western drugs on white blood cell count in 31 patients with gastric cancer. These patients were divided into 3 groups: (1) Fu Zheng (strengthen the body resistance) with invigorating the Spleen and Kidney recipe; (2) Fu Zheng with western drugs raising WBC and enhancing immunity; (3) Gong Xiao (eliminating the evil factors and mass) with promoting blood circulation to remove blood stasis recipe or eliminating the evil factors and mass recipe. After chemotherapy, the mean of WBC count was greater than 4.0 X 10(9)/L in group I; less than 3.5 X 10(9)/L in group II; less than 3.0 X 10(9)/L in group III. Because of WBC count below 3.0 X 10(9)/L, in group II there were 5 cases (5/14) whose chemotherapies had to be discontinued, and in group III there were 4 cases (4/6). While all patients were completed their chemotherapies in group I. Its statistical difference was significant (P less than 0.05). It suggested that invigorating the Spleen and Kidney recipe had specific effect on decreasing the toxicity and side effect of chemotherapy, preventing bone marrow suppression and leukopenia, and was better than western drugs used in group II. It showed in the treatment of cancer with TCM, we must pay attention to the relationship between the Fu Zheng and the Gong Xiao.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Drugs, Chinese Herbal/therapeutic use , Leukopenia/drug therapy , Stomach Neoplasms/drug therapy , Adult , Aged , Cytarabine/administration & dosage , Cytarabine/adverse effects , Female , Fluorouracil/administration & dosage , Fluorouracil/adverse effects , Humans , Leukopenia/chemically induced , Male , Middle Aged , Mitomycin , Mitomycins/administration & dosage , Mitomycins/adverse effects
9.
J Pediatr Surg ; 19(3): 281-4, 1984 Jun.
Article in English | MEDLINE | ID: mdl-6747790

ABSTRACT

In 31 cases of Hirschsprung's disease, the mean value of erythrocyte AChE activity was discovered to be 91.24 +/- 10.24 u/mL, being significantly higher than that from 127 normal children of 73.51 +/- 9.36 u/mL (P less than 0.001); whereas serum ChE mean value of 14.49 +/- 4.04 u/mL showed no difference from normal control (16.89 +/- 8.86 u/mL, P greater than 0.05). In addition, the erythrocyte AChE activity of six newborns with Hirschsprung's disease was also found to be much higher than its own normal control. It was therefore, concluded that this assay may be of supplementary diagnostic significance in diagnosing neonatal Hirschsprung's disease.


Subject(s)
Acetylcholinesterase/blood , Erythrocytes/enzymology , Hirschsprung Disease/enzymology , Child , Child, Preschool , Cholinesterases/blood , Clinical Enzyme Tests , Constipation/complications , Diagnosis, Differential , Female , Hirschsprung Disease/blood , Hirschsprung Disease/diagnosis , Humans , Infant , Infant, Newborn , Male
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