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1.
Zhonghua Yi Shi Za Zhi ; 54(1): 29-33, 2024 Jan 28.
Article in Chinese | MEDLINE | ID: mdl-38475683

ABSTRACT

Modern Bai Jiu(liquor) was called Shao Jiu in ancient times.By consulting ancient books, it was found that there was a distillation and preparation process of Shao Jiu before the Ming Dynasty, but due to its high toxicity, the scope of application was limited, and there were few records of its medicinal use.However many records of its medicinal use was found in the Compendium of Materia Medica(«¼).By comparing the medical books that recorded Shao Jiu in previous dynasties, it is found that the Compendium of Materia Medica comprehensively records the relevant cognition and application of the medicinal use of Shao Jiu for the first time. The book lists in detail the causes of the toxicity of Shao Jiu and the methods to avoid it, comprehensively expounds its characteristics, efficacy and indications, lists a variety of ways to use it, skillfully uses Shao Jiu to treat syphilis sores, and proposes that high-concentration Shao Jiu can be used as a solvent for medical liquor.The record of Shao Jiu in the Compendium of Materia Medica had a profound impact on the medical liquor of later generations.The use of Shao Jiu in the Qing Dynasty continued to expand, and the types of medicinal liquor were also constantly enriched. The record of Shao Jiu in the Compendium of Materia Medica can also provide a reference for the medicinal use of modern liquor.


Subject(s)
Materia Medica , Books , China , Medicine, Chinese Traditional
2.
Zhonghua Yi Shi Za Zhi ; 52(6): 374-379, 2022 Nov 28.
Article in Chinese | MEDLINE | ID: mdl-36624679

ABSTRACT

The North China Medical College typically represented medical colleges for traditional Chinese medicine in the 1930s when many of them were set up. It was based on the principles of centring on traditional Chinese medicine, following western medicine and integrated medicine in teaching. This led to the emergence of a great number of people with a high level of traditional Chinese medicine and strong belief in it. In terms of the textbooks and handouts for western medicine, compared to similar textbooks in other medical colleges, such as the Medical College of Xie He, at that time, the textbooks in the North China Medical College covered a variety of perspectives and categories. It was found that 20 textbooks for western medicine in the North China Medical College were designed reasonably in content and were simple and applicable in teaching. More importantly, it contained some traditional Chinese medicine in different degrees, with its typical characteristics. The course design and textbook compilation provided references for the teaching in contemporary medical universities.


Subject(s)
Medicine , Humans , Universities , China , Medicine, Chinese Traditional
3.
J Clin Pharm Ther ; 43(1): 21-25, 2018 Feb.
Article in English | MEDLINE | ID: mdl-28726273

ABSTRACT

WHAT IS KNOWN AND OBJECTIVE: Oral nifedipine is commonly used to treat pre-eclampsia, one of the most severe complications during pregnancy, but its clinical efficacy is less than ideal. Epigallocatechin gallate (EGCG), a natural compound from green tea, could benefit cardiovascular health especially hypertension. We investigated the clinical efficacy of EGCG, when complemented with oral nifedipine, in treating pre-eclampsia. METHODS: A total of 350 pregnant women with severe pre-eclampsia were recruited and randomized to receive oral nifedipine, together with placebo (NIF+placebo) or EGCG (NIF+EGCG). The primary treatment outcome was the time needed to control blood pressure and interval time before a new hypertensive crisis, whereas the secondary treatment outcome was the number of treatment doses to effectively control blood pressure, maternal adverse effects and neonatal complications. RESULTS AND DISCUSSION: Comparing NIF+EGCG group to NIF+placebo group, the time needed to control blood pressure was significantly shorter (NIF+EGCG 31.2±16.7 minutes, NIF+placebo 45.3±21.9 minutes; 95% CI 9.7-18.5 minutes), whereas interval time before a new hypertensive crisis was significantly prolonged (NIF+EGCG 7.2±2.9 hours, NIF+placebo 4.1±3.7 hours; 95% CI 2.3-3.9 hours), and the number of treatment dosages needed to effectively control blood pressure was also lower. Between the two treatment groups, no differences in incidence rates of maternal adverse effects or neonatal complications were observed. WHAT IS NEW AND CONCLUSIONS: EGCG is both safe and effective in enhancing treatment efficacy of oral nifedipine against pregnancy-induced severe pre-eclampsia, but formal validation is required prior to its recommendation for use outside of clinical trials.


Subject(s)
Antihypertensive Agents/therapeutic use , Catechin/analogs & derivatives , Nifedipine/therapeutic use , Pre-Eclampsia/drug therapy , Administration, Oral , Adult , Blood Pressure/drug effects , Catechin/pharmacology , Double-Blind Method , Female , Humans , Pregnancy , Treatment Outcome
4.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi ; 35(10): 765-767, 2017 Oct 20.
Article in Chinese | MEDLINE | ID: mdl-29294552

ABSTRACT

Objective: To investigate the clinical effect and safety of electroencephalographic biofeedback therapy in improving memory disorders in patientsin the recovery stage of acute severe toxic encephalopathy. Methods: A total of 52 patients in the recovery stage of acute severe toxic encephalopathy who were hospitalized in our hospital from March 2013 to December 2016 were enrolled and randomly divided into observation group with 27 patients and control group with 25 patients. Both groups were given the drugs to promote the metabolism of brain cells,and the patients in the observation group were given electroencephalographic biofeedback therapy in addition. The Chinese revised version of Wechsler Memory Scale Type A was used to measure memory ability before and after each course of treatment. The treatment outcome was evaluated for both groups. Results: There were no significant differences in the scores of long-term memory,short-term memory, immediate memory, and memory quotient between the two groups before treatment(P>0.05).After the first course of treatment ended, the observation group had significant increases in the scores of forward task,backward task,association,and memory quotient(P<0.05); compared with the control group, the observation group had a significant reduction in the score of backward task(P<0.05).After the second course of treatmentended, the observation group had significant increases in the scores offorward task,backward task,memorization of pictures,reproduction,association,comprehension,and memory quotient,and the control group had significant increases in the scores of reproduction,association,comprehension,and memory quotient(P<0.05); compared with the control group, the observation group had significant increases in the scores of forward task,backward task,memorization of pictures, reproduction, association, comprehension, and memory quotient(P<0.05).Two patients experiencedchest distress, palpitation, and dysphoria during treatment, which did not affect the treatment. Conclusion: Electroencephalographic biofeedback therapy has a certain effect in the treatment of memory disorders in patients with acute severe toxic encephalopathy.


Subject(s)
Memory Disorders/therapy , Neurofeedback/methods , Neurotoxicity Syndromes/complications , Acute Disease , Biofeedback, Psychology , Brain , Humans , Memory , Memory Disorders/physiopathology , Treatment Outcome
5.
J Clin Pharm Ther ; 41(6): 657-661, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27578562

ABSTRACT

WHAT IS KNOWN AND OBJECTIVE: Pre-eclampsia is one of the most challenging diseases of pregnancy. Both nifedipine and labetalol have been used for treatment of pregnancy-induced severe pre-eclampsia. METHODS: In the present study, the efficacy and safety of oral nifedipine and intravenous labetalol for severe pre-eclampsia therapy were compared. Eligible pregnant women with severe pre-eclampsia (n = 147) were allocated to receive either oral nifedipine or intravenous labetalol. The primary endpoint of the study was the time needed to achieve target blood pressure. Secondary outcomes were the time interval before a new hypertensive crisis following effective blood pressure control, number of doses and adverse effects. RESULTS AND DISCUSSION: We found that the time taken to achieve effective blood pressure control was 35 vs. 42 min for oral nifedipine and intravenous labetalol, respectively (P = 0·37). Compared with labetalol group, no significant difference was observed regarding time interval and drug dosages in nifedipine arm. Moreover, no serious side effects on maternal or perinatal were observed in either group. WHAT IS NEW AND CONCLUSIONS: These findings suggest that both oral nifedipine and intravenous labetalol are effective for safely reducing blood pressure to target levels in patients with severe pre-eclampsia.


Subject(s)
Antihypertensive Agents/administration & dosage , Labetalol/administration & dosage , Nifedipine/administration & dosage , Pre-Eclampsia/drug therapy , Pregnancy Complications/drug therapy , Administration, Intravenous , Administration, Oral , Adult , Blood Pressure/drug effects , Double-Blind Method , Female , Humans , Hypertension/drug therapy , Pregnancy , Young Adult
6.
Hum Exp Toxicol ; 32(9): 904-13, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23444337

ABSTRACT

To determine the no-observed-adverse-effect level (NOAEL) of exposure and target organs of neem oil for establishing safety criteria for human exposure, the subchronic toxicity study with neem oil in mice was evaluated. The mice (10 per sex for each dose) was orally administered with neem oil with the doses of 0 (to serve as a control), 177, 533 and 1600 mg/kg/day for 90 days. After the treatment period, observation of reversibility or persistence of any toxic effects, mice were continuously fed without treatment for the following 30 days. During the two test periods, the serum biochemistry, organ weight and histopathology were examined. The results showed that the serum biochemistry and organ coefficient in experimental groups had no statistical difference compared with those of the control group. At the 90th day, the histopathological examinations showed that the 1600 mg/kg/day dose of neem oil had varying degrees of damage on each organ except heart, uterus and ovarian. After 30-day recovery, the degree of lesions to the tissues was lessened or even restored. The NOAEL of neem oil was 177 mg/kg/day for mice and the target organs of neem oil were determined to be testicle, liver and kidneys.


Subject(s)
Azadirachta/chemistry , Glycerides/toxicity , Terpenes/toxicity , Toxicity Tests, Subchronic , Administration, Oral , Animals , Dose-Response Relationship, Drug , Eating/drug effects , Female , Glycerides/isolation & purification , Male , Mice , Mice, Inbred Strains , No-Observed-Adverse-Effect Level , Organ Specificity , Plants, Medicinal , Seeds/chemistry , Terpenes/isolation & purification
7.
Osteoporos Int ; 23(4): 1317-27, 2012 Apr.
Article in English | MEDLINE | ID: mdl-21505910

ABSTRACT

UNLABELLED: This multicenter and randomized clinical trial showed that daily oral herbal formula Xian Ling Gu Bao (XLGB) was safe in postmenopausal women over a 1-year treatment. Those patients (n ∼ 50) treated with XLGB at the conventional dose demonstrated a statistically significant increase in dual-energy X-ray absorptiometry (DXA) bone mineral density (BMD) at lumbar spine at 6 months and a numerically increased BMD at 12 months. INTRODUCTION: The aim of this study was to examine the safety and efficacy of a herbal formula XLGB in postmenopausal women (ChiCTR-TRC-00000347). METHODS: One hundred eighty healthy postmenopausal women (≥60 years old) with BMD T-score ≤ -2.0 (lumbar spine or femoral neck) were recruited from four clinical centers to receive low-dose (conventional dose) XLGB (L-XLGB group, 3 g/day, n = 61) or high-dose XLGB (H-XLGB group, 6 g/day, n = 58) or placebo (CON group, n = 61). Women received daily calcium (500 mg) and vitamin D (200 IU) supplementation. Primary endpoints were lumbar spine BMD and safety; secondary endpoints were femoral neck BMD and bone turnover markers measured at baseline and at 6 and 12 months. RESULTS: Of 180 women recruited, 148 completed the study. The compliance in each group was comparable. Prominent adverse events were not observed in either group. In the L-XLGB group at 6 months, lumbar spine BMD by DXA increased significantly from baseline (+2.11% versus CON +0.58%, p < 0.05), but femoral neck BMD did not; at 12 months, BMD in the L-XLGB group decreased from 6-month levels yet remained higher than baseline, but without difference from the CON group. There was no dose-dependent response. Bone turnover marker levels declined during the first 6 months after XLGB treatment. There was no significant difference in the overall incidence of side effects among treatment and control groups. CONCLUSION: XLGB over 1-year treatment at the conventional dose demonstrated safe and only a statistically significant increase in BMD at lumbar spine at 6 months in postmenopausal women.


Subject(s)
Bone Density Conservation Agents/therapeutic use , Drugs, Chinese Herbal/therapeutic use , Osteoporosis, Postmenopausal/drug therapy , Absorptiometry, Photon/methods , Aged , Biomarkers/blood , Bone Density/drug effects , Bone Density Conservation Agents/administration & dosage , Bone Density Conservation Agents/adverse effects , Bone Remodeling/drug effects , Bone Remodeling/physiology , Double-Blind Method , Drugs, Chinese Herbal/administration & dosage , Drugs, Chinese Herbal/adverse effects , Female , Femur Neck/physiopathology , Humans , Lumbar Vertebrae/physiopathology , Medication Adherence/statistics & numerical data , Middle Aged , Osteocalcin/blood , Osteoporosis, Postmenopausal/blood , Osteoporosis, Postmenopausal/physiopathology , Treatment Outcome
8.
Reprod Domest Anim ; 45(2): 275-82, 2010 Apr.
Article in English | MEDLINE | ID: mdl-19090820

ABSTRACT

The objective of this study was to develop a culture system which could support buffalo spermatogonia differentiation into spermatids in vitro. Testes from 3- to 5-month-old buffaloes were decapsulated and seminiferous tubules were enzymatically dissociated to recover spermatogonia and sertoli cells. The cells were cultured in modified Dulbecco modified Eagle medium supplemented with different concentrations of foetal bovine serum, retinol, testosterone for 2 months at 37 degrees C. Spermatogonia and sertoli cells were identified with an antibody against c-kit or GATA4, respectively. The viability of spermatogonia in the media supplemented with different concentrations of serum was all significantly higher (p < 0.05) compared with that in the medium without serum. A-paired or A-aligned spermatogonia and spermatogonial colonies (AP-positive) were observed after 7-10 days of culture and spermatid-like cells with a flagellum (6-8 microm) appeared after 30 days of culture. For cultured conditions, retinol could not significantly promote the formation of spermatid-like cells (p > 0.05), whereas supplementation of testosterone could significantly promote (p < 0.05) the formation of spermatid-like cells after 41 days of culture. The expression of the spermatid-specific marker gene (PRM2) was identified after 30 days of culture by RT-PCR. Yet, the transition protein 1 (TP1, a haploid makers) was not detected. Meanwhile, spermatids developed in vitro were also confirmed by Raman spectroscopy. These results suggest that buffalo spermatogonia could differentiate into spermatids in vitro based on the analysis of their morphology, PRM2 expression and Raman spectroscopy. Yet, the normality of the spermatid-like cells was not supported by TP1 expression.


Subject(s)
Buffaloes/physiology , Cell Culture Techniques/veterinary , Spermatogonia/cytology , Spermatogonia/physiology , Animals , Culture Media/chemistry , Male , Sperm Maturation/physiology , Testosterone/chemistry , Vitamin A/chemistry
9.
Zhong Yao Cai ; 24(6): 411-3, 2001 Jun.
Article in Chinese | MEDLINE | ID: mdl-11563187

ABSTRACT

The existence of podophyllotoxin lignans in Dysosma versipellis and its allied plants was analyzed by twice developing TLC, and the content by chromotropic-colorimetric assay. The results showed that podophyllotoxin lignans exist in the rhizoma, radix, stem and leaf of Dysosma versipellis and its allied plants. The total lignans content is 2%-7%, and there is a big variation between different species. The total lignans content of Dysosma versipellis is related to the habitat.


Subject(s)
Berberidaceae/chemistry , Lignans/analysis , Plants, Medicinal/chemistry , Podophyllotoxin/analysis , Plant Roots/chemistry , Plant Stems/chemistry
10.
Zhong Yao Cai ; 24(2): 89-92, 2001 Feb.
Article in Chinese | MEDLINE | ID: mdl-11402736

ABSTRACT

The descriptions, histological and microscopical characteristics of three allied species of Dysosma versipellis were described.


Subject(s)
Berberidaceae/anatomy & histology , Plants, Medicinal/anatomy & histology , Berberidaceae/classification , Plants, Medicinal/classification
11.
Chemosphere ; 42(2): 209-14, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11237300

ABSTRACT

A long-term randomised block field experiment was established in 1997 to study the dynamics of total P and dissolved P in the surface waters of rice fields receiving two application rates of fertiliser P and one rate of combined fertiliser and manure P. Preliminary results from the first two crops show that concentrations of both total P and dissolved P in the surface waters increased significantly following P application, especially during the first 2 weeks after application. P concentrations subsequently declined sharply within about 10 days, then declined steadily and remained almost constant from about 1 month after application. The initial increase in P concentration of surface waters was higher with increasing rate of fertiliser P, and the P concentration at the highest fertiliser rate peaked within about 1 week of application. The elevated P concentrations following fertiliser P application declined more rapidly than those following the combined application of fertiliser and manure P. When fertiliser and manure P were applied together, about 7 days later the surface water P concentrations were significantly higher than when the same rate of P (or double) was applied as fertiliser only. Disturbance of the surface soil by hand harrowing further increased the P concentrations in surface waters, with a subsequent decline to a steady value after about 1 week. Application of P fertiliser to the high P status soil in this experiment gave no crop yield response and may have increased the risk of pollution of adjacent surface waters through drainage from heavy rainfall events during the rice growing season. Therefore, fertiliser P should not be applied to such soils. If, however, fertiliser or manure P is applied, the application should be made during the dry winter to reduce P losses. Manure should be applied with particular care because of the higher risk of P losses to surface water arising from the relatively long period of high P concentrations in surface waters and the potential for greater release of P to field surface waters from the soil. Hand harrowing should also be avoided during wet weather to protect water quality.


Subject(s)
Fertilizers , Manure , Oryza/metabolism , Phosphorus/metabolism , Water , Animals , Rain , Random Allocation , Surface Properties
12.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 21(8): 591-4, 2001 Aug.
Article in Chinese | MEDLINE | ID: mdl-12575573

ABSTRACT

OBJECTIVE: To study the effect of Xiongshao Capsule (XS) on vascular remodeling in porcine coronary balloon injury model. METHODS: Restenosis model was established by oversized balloon injury at mid-region of the left anterior descending coronary artery. The effect of drugs on late lumen loss and vascular remodeling was evaluated with quantitative histological method by combining results from histopathological analysis and coronary arteriography. RESULTS: Vascular remodeling explained (59 +/- 20)% of late lumen loss. All drugs significantly reduced late lumen loss 4 weeks after balloon injury (P < 0.05 or 0.01). Both low-dose and high-dose XS markedly reduced late lumen loss resulting from vascular remodeling, as compared with the control group (P < 0.05 and P < 0.01 respectively). CONCLUSION: Vascular remodeling played an important role in late lumen stenosis after balloon injury of coronary artery. XS could significantly inhibit pathological vascular remodeling after balloon injury, thus reduce late lumen loss and prevent restenosis.


Subject(s)
Angioplasty, Balloon, Coronary/adverse effects , Coronary Restenosis/pathology , Coronary Vessels/pathology , Drugs, Chinese Herbal/pharmacology , Animals , Capsules , Coronary Restenosis/prevention & control , Female , Male , Phytotherapy , Swine
13.
Zhonghua Yi Shi Za Zhi ; 31(1): 33-5, 2001 Jan.
Article in Chinese | MEDLINE | ID: mdl-11877109

ABSTRACT

Based on the comparison between the prescriptions of Zhongjing's Prescriptions and Jotting Prescriptions, it can be seen that Xiao pin fang (Jotting Prescriptions) in many aspects, reflecting partly the tendency of changes in prescriptions from the Eastern Han dynasty to Liu Song period of the Northern and Southern dynasties.


Subject(s)
Drug Prescriptions/history , China , History, Ancient , History, Medieval
15.
J Biomed Mater Res ; 53(5): 457-66, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10984692

ABSTRACT

To produce bioactive materials for bone substitutes, two major deposition methods, suspension method and thermal deposition method, were employed to develop bioactive, mechanically strong, and porous ceramics. Hydroxylapatite (HA) has been uniformly coated onto inner pore surfaces of reticulated alumina substrates. It has been found that the in vitro bioactivity of HA coatings was affected by both structural crystallinity and specific surface area. Well-crystallized HA heat-treated at high temperatures has resulted in reduced bioactivity. The bio-reaction rate was found to increase with the surface area of HA. We have found that the stability of the well-crystallized HA is associated with the high driving force required for the formation of hydroxy-carbonate apatite (HCA) phase.


Subject(s)
Aluminum Oxide/chemistry , Aluminum Oxide/pharmacokinetics , Bone Substitutes , Coated Materials, Biocompatible/chemistry , Coated Materials, Biocompatible/pharmacokinetics , Durapatite/chemistry , Durapatite/pharmacokinetics , Aluminum Oxide/blood , Body Fluids , Calcium/analysis , Coated Materials, Biocompatible/chemical synthesis , Crystallization , Durapatite/blood , Hot Temperature , Humans , Microscopy, Electron, Scanning , Spectroscopy, Fourier Transform Infrared , Surface Properties
16.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 20(10): 757-60, 2000 Oct.
Article in Chinese | MEDLINE | ID: mdl-11938813

ABSTRACT

OBJECTIVE: To observe the effect of Xiongshao Capsule (XSC) on proliferation and apoptosis of aortic smooth muscle cells (SMC) of rabbits by serum pharmacological method. METHODS: SMC were isolated from thoracic aorta of the normal rabbits and passaged. The SMC proliferation model was established by endothelin (ET). The medicated serum was prepared after given the normal rabbits suspension of XSC through gastrogavage for 10 days. The proliferation and apoptosis of SMC were observed by methyl thiazolyl tetrazolium (MTT) colorimetry, flow cytometry and agarose gel electrophoresis. RESULTS: ET obviously promoted proliferation of SMC, and the serum medicated with XSC could lower the proportion of SMC in S + G2 phase and markedly inhibited the proliferation of SMC caused by ET in dose dependent manner. It also had certain effect on inducing apoptosis of SMC. CONCLUSION: XSC could markedly inhibit the proliferation of SMC caused by ET and induce apoptosis of SMC, which might be the mechanism of preventing coronary restenosis after interventional treatment.


Subject(s)
Apoptosis/drug effects , Drugs, Chinese Herbal/pharmacology , Muscle, Smooth, Vascular/cytology , Animals , Aorta, Thoracic/cytology , Capsules , Cell Cycle , Cell Division/drug effects , Cells, Cultured , Endothelins/antagonists & inhibitors , Male , Rabbits
17.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 20(7): 494-7, 2000 Jul.
Article in Chinese | MEDLINE | ID: mdl-11789203

ABSTRACT

OBJECTIVE: To evaluate the effect of Xiongshao capsule (XSC) in preventing clinical and angiographic restenosis after coronary angioplasty or/and stenting. METHODS: Sixty-five coronary heart disease (CHD) patients with successful angioplasty or and stenting were randomly divided into the control group (37 cases, routine treatment) and the XSC group (28 cases, routine treatment plus XSC). The recurrent of angina, changing of blood stasis syndrome score (BSSS) and coronary angiography within 6 months after coronary angioplasty or/and stenting were observed. RESULTS: Recurrent angina occurred in 6 out of 28 patients in the XSC group, which was much better than that in the control group, 18 out of 37 patients (P < 0.05). Follow-up angiography was performed in 26 including 10 patients in the XSC group (restenosis was observed in 4 cases), and 16 cases in the control group (restenosis in 13 cases), there was significant difference between the XSC group and the control group (P < 0.05). For BSSS at follow-up, XSC group was much lower than that of the control group (P < 0.01). Logistic regress analysis showed the combination with XSC and the base-line BSSS were important affecting factors on the occurrence of restenosis (P < 0.05). The odds ratio of the occurrence of angiographic restenosis (BSSS > 25 to BSSS < or = 25) was 6.5. CONCLUSIONS: XSC could markedly reduce the occurrence of restenosis, recurrence of angina and improve the condition of blood stasis after coronary angioplasty or/and stenting. The severity of blood stasis syndrome was an important affecting factor on the occurrence of restenosis. BSSS > 25 can be served as one of the predicting factors of the occurrence of restenosis after coronary angioplasty or/and stenting.


Subject(s)
Angina, Unstable/therapy , Angioplasty, Balloon, Coronary , Coronary Restenosis/prevention & control , Drugs, Chinese Herbal/therapeutic use , Adult , Aged , Angina, Unstable/drug therapy , Capsules , Female , Follow-Up Studies , Humans , Male , Middle Aged , Recurrence , Stents
18.
J Reconstr Microsurg ; 15(7): 539-45, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10566584

ABSTRACT

Recent evidence has shown that changes in blood viscosity and marked increases in both platelet count and fibrinogen concentration occur after exposure to hyperbaric oxygen (HBO). The purpose of the present study was to address whether repeated HBO therapy would increase either hematocrit or platelet count, and to determine if these changes would influence the patency of the microvascular anastomosis, as well as anastomotic healing. Eighty femoral arteries from 40 rats were divided into four groups (n = 10), and arterial anastomoses were performed on normal arteries in the first two groups, and on crushed arteries in the second two groups. One of the normal artery groups and one of the crushed artery groups received repeated HBO treatments for 5 days. Anastomotic patency rates, platelet count, hematocrit, and breaking strength were recorded. Among the results of this study were that: (1) there was no difference in patency rate following HBO treatment in both the normal and crushed artery groups; (2) platelet count was significantly higher following HBO treatment in the groups with the undamaged arteries; (3) breaking strength was significantly increased following HBO treatment in the groups with the crushed arteries. The authors concluded that HBO therapy may be useful in improving the healing of microvascular anastomoses in vessels that have undergone crush injury. Although HBO treatment results in an increased platelet count, this does not influence anastomotic patency.


Subject(s)
Femoral Artery/surgery , Hyperbaric Oxygenation , Vascular Surgical Procedures/methods , Wound Healing , Anastomosis, Surgical , Animals , Chi-Square Distribution , Disease Models, Animal , Femoral Artery/pathology , Hematocrit , Male , Microcirculation/physiology , Platelet Count , Rats , Rats, Sprague-Dawley , Reference Values , Vascular Patency
19.
J Biomed Mater Res ; 48(2): 117-20, 1999.
Article in English | MEDLINE | ID: mdl-10331903

ABSTRACT

A thin film of hydroxyapatite (HA) was uniformly coated onto a highly porous substrate of alumina through the thermal decomposition method. Calcium 2-ethyl hexanoate and bis(2-ethyhexyl) phosphite were used as starting materials. Scanning electron microscopy, X-ray diffraction, and infrared spectroscopy were used to characterize the chemical and structural evolution of the coating. In vitro tests were conducted to evaluate the reactivity of the synthetic HA. It was found that the sintering process greatly influenced the in vitro behavior of HA. High temperature sintering may reduce the reactivity of HA, suggesting that the reactivity is structure dependent.


Subject(s)
Aluminum Oxide/chemistry , Biocompatible Materials/chemistry , Durapatite/chemistry , Microscopy, Electron, Scanning , Spectroscopy, Near-Infrared , Temperature , X-Ray Diffraction
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