• 한국어병학회지
• /
• 제5권1호
• /
• pp.37-48
• /
• 1992

항생제란 어떤 미생물의 생성물질로서 다른 미생물의 증식을 억제하거나 살균작용을 나타내는 것을 의미한다. 현재까지 알려진 4000여종의 항생제중, 수산용으로는 약 20여종이 사용되고 있다. 이러한 항생제의 분류는 화학적 구조와 부수되는 기능에 의하는 것이 일반적이며 그 효과는 적용되는 병원성균의 종류와 어류가 처해있는 환경에 따라 대단히 영향을 받는다. 그러므로 항생제의 종류와 적용방법은 정확한 질병에 대한 원인 규명이 있은 후 결정되어져야 할 것이다. 무절제하게 사용된 항생제는 자연적으로 발생하여 존재하고 있는 내성균을 선택적으로 증식 가능케 한다. 이미 일본의 수많은 양어장에서 내성균 출현의 보고가 있었고, 많은 종류의 내성균은 R plasmid를 가지고 있다는 것도 밝혀졌다. 우리나라의 양어장에서도 내성균 출현과 R plasmid에 의한 내성균 확산은 곧 문제가 될 수 있는 가능성이 크므로 전반적인 역학조사가 있어야 할 것이다. 상용항생제의 어류에 대한 약동력학, 잔존량, 임상적용 실험등에 대한 연구는 상당히 되어 있어 적절한 이들 항생제의 사용이 가능하지만, 현재까지 대부분의 수산용 항생제에 대해서는 연구해야 될 부분이 아직 많이 남아 있다. 그러므로 어류질병 치료와 항생제의 정확한 사용을 위해서는 양식사업을 하고 있는 현장과 진단을 할 수 있는 실험실의 긴밀한 협조관계가 무엇보다 중요하다 할 것이다.

• 동의생리병리학회지
• /
• 제19권4호
• /
• pp.982-992
• /
• 2005

Acupuncture as a therapeutic intervention is widely used for the treatment of many functional disorders such as substance abuse and mental dysfunction. Clinical trials are currently underway to determine the effectiveness of acupuncture in the treatment of drug addiction. Yet, there are still many unanswered questions about the basic mechanism of acupuncture. Studies have shown that both the psychomotor stimulant effects and rewarding properties of addictive drugs, including morphine, are sensitized by repeated drug administration and raised the possibility that both of these effects may De linked to the same or closely overlapping the mesolimbic dopamine systems. Neiguan (PC6) point on the pericardium channel which is associated with the brain and its mental function, has been used to treat mental, psychosomatic disorders and gastroenterological disorders. The present study was designed to investigate the effect of acupuncture on repeated morphine-induced changes in extracellular dopamine levels using in vivo microdialysis and to measure the effect of acupuncture on repeated morphine-induced behavioral changes. Male Sprague-Dawley rats were treated twice a day for three days with increasing doses of morphine (10, 20 and 40 mg/kg, s.c.) or with saline. After 15 days of withdrawal, rats were challenged with morphine hydrochloride (5 mg/kg, s.c.). Acupuncture was applied at bilateral Neiguan (PC6) points for 1min after the morphine challenge. Results showed that acupuncture at the specific acupoint PC6, but not at control points (tail and HE8) significantly decreased both dopamine release, behavior induced by a systemic morphine challenge or a single s.c. morphine injection in the morphine-repeated animals. These results suggest that reduction in sensitization may be one mechanism whereby acupuncture alleviates morphine craving in addicts. Moreover, in a more general sense these results suggest that acupuncture can be used as a therapeutic intervention for correcting reversible malfunction of the body by direction of brain pathway and thus acupuncture can contribute to the biochemical balance in the central nervous system by regulating neurotransmitters.

• Journal of Yeungnam Medical Science
• /
• 제18권1호
• /
• pp.51-58
• /
• 2001

담즙정체성 간염의 원인과 임상양상, 검사실 소견 및 경과를 알아보고자 1991년에서 2000년까지 영남대학교 의과대학 부속병원에서 혈액검사 및 간생검으로 담즙정체성 간염이 확진된 14명의 환자를 대상으로 후향적 연구를 시행하여 다음과 같은 결과를 얻었다. 담즙정체성 간염에서 비정상 간기능검사의 기간은 1개월에서 30개월까지 다양하게 나타났고, 항결핵제, 항생제에 의한 담즙정체성 간염이외에도 한약제, 건강식품에 의한 경우 검사실 소견과 임상경과가 중하게 나타나는 경우가 있으므로, 이들 약물을 사용한 병력이 있는 경우 정기적인 간기능 검사가 필요하다. 담즙정체성 간염이 만성 간내 담즙정체를 보이는 경우 바이러스에 의한 담즙정체성 간염과 담관소멸 증후군으로의 진행 유무, 원발성 담즙성 간경변증, 자가면역성 간염과의 감별이 필요하며, 지속적인 간기능 검사이상을 보일 경우에는 연속적인 간생검이 필요할 것으로 생각된다.

• Korean Journal of Acupuncture
• /
• 제29권2호
• /
• pp.179-187
• /
• 2012

목적 : 침 치료는 약물 중독을 위한 효과적인 치료법으로 인정받은 이래 이에 관한 많은 연구들이 이루어지고 있다. 본 논문에서는 모르핀 중독의 침 치료에 사용된 경혈 및 소속 경락에 대해 육경(六經)적인 관점에서 이를 해석하였다. 방법 : 미국 국립 의학도서관(PubMed)에서 "모르핀, 침"을 주제어로 하여 255개의 논문을 검색하였고, 한국학술정보(주)(KISS)에서 "모르핀"을 주제어로 하여 629개의 논문을 검색하였다. 영어로 기술된 논문만을 연구 대상으로 하였다. 모르핀에 대한 중독(남용, 의존, 민감화, 중독, 섭취, 금단 증상, 금단 증후군, 재발, 갈망)과 관련된 논문만을 연구 대상으로 하였다. 침 또는 전침을 사용한 논문만을 연구 대상으로 하였으며, 이침을 사용한 것은 제외하였다. 임상 연구와 실험 연구를 모두 연구 대상으로 하였다. 결과 : 모르핀의 침 연구에서 가장 많이 사용된 경혈은 족삼리-삼음교(足三里-三陰交)(전침, 10회)로 나타났고, 그 다음은 신문(神門)(5회)이었으며, 그밖에 합곡(合谷)(2회), 신유(腎兪)(1회), 내관(內關)(1회) 등의 경혈이 사용되었다. 족삼리(足三里)는 장부상통에 의해 심포경과 통하는 위경을 조절함으로써 스트레스 반응에 관계된 심포경을 조절할 수 있음에 따라 모르핀 중독 연구에 사용된 것으로 보인다. 음양이총혈의 하나인 삼음교(三陰交)는 정신 기능에 영향을 미치는 혈분을 다스리며 식욕을 조절하는 기능 또한 이러한 효능에 관련된 것으로 사료된다. 수소음심경의 원혈인 신문(神門)은 뇌와 관계된 소속 경맥의 기능 및 혈명으로부터 정신 기능을 조절할 수 있음을 알 수 있다. 양계(陽谿)는 양명경의 원혈로서 상통하는 궐음경을 조절함으로써 스트레스 반응을 조절할 수 있기 때문에 사용된 것으로 보이며, 신유(腎兪)는 소속 경맥이 뇌와 관련되어 있기 때문에 사용된 것으로 사료된다. 내관(內關)은 모르핀 중독에 수반되는 스트레스를 조절할 수 있기 때문에 사용된 것으로 보인다. 결론 : 모르핀 연구에 사용된 경혈은 다양한 기전을 통해 뇌 기능에 영향을 미치는 것으로 보이며, 스트레스 반응을 조절하는 것이 이에 관련된 것으로 사료된다.

• IMMUNE NETWORK
• /
• 제14권1호
• /
• pp.45-53
• /
• 2014

Osteoarthritis (OA) is a degenerative joint disease characterized by a progressive loss of cartilage. And, increased oxidative stress plays a relevant role in the pathogenesis of OA. Ursodeoxycholic acid (UDCA) is a used drug for liver diseases known for its free radical-scavenging property. The objectives of this study were to investigate the in vivo effects of UDCA on pain severity and cartilage degeneration using an experimental OA model and to explore its mode of actions. OA was induced in rats by intra-articular injection of monosodium iodoacetate (MIA) to the knee. Oral administration UDCA was initiated on the day of MIA injection. Limb nociception was assessed by measuring the paw withdrawal latency and threshold. Samples were analyzed macroscopically and histologically. Immunohistochemistry was used to investigate the expression of interleukin-$1{\beta}$ (IL-$1{\beta}$), IL-6, nitrotyrosine and inducible nitric oxide synthase (iNOS) in knee joints. UDCA showed an antinociceptive property and attenuated cartilage degeneration. OA rats given oral UDCA significantly exhibited a decreased number of osteoclasts in subchondral bone legion compared with the vehicle-treated OA group. UDCA reduced the expression of IL-$1{\beta}$, IL-6, nitrotyrosine and iNOS in articular cartilage. UDCA treatment significantly attenuated the mRNA expression of matrix metalloproteinase-3 (MMP-3), -13, and ADAMTS5 in IL-$1{\beta}$-stimulated human OA chondrocytes. These results show the inhibitory effects of UDCA on pain production and cartilage degeneration in experimentally induced OA. The chondroprotective properties of UDCA were achieved by suppressing oxidative damage and inhibiting catabolic factors that are implicated in the pathogenesis of cartilage damage in OA.

• 대한한의학회지
• /
• 제26권4호
• /
• pp.122-129
• /
• 2005

Objectives: Graves' disease is the most common cause of hyperthyroidism, and its pathogenesis includes thyroid specific autoimmunity. Anti-thyroid drugs are widely used for regulating the thyroid function. However, in spite of long-term therapy with anti-thyroid drugs, about 40$\sim$$70\%$ of the treated patients have a relapse, and some suffer adverse effects. In this study, to evaluate the clinical efficacy of Ahnjeonbaekho-tang(AJBHT) on Graves' disease patients, we performed the clinical study prospectively. Methods: Through the thyroid function test(TFT) of 54 patients diagnosed as Graves' disease in other hospitals, 21 patients were assigned into the study. After the withdrawal of anti-thyroid drugs, AJBHT was administerd to patients for 2 months. At the same time, TFT, TSH binding inhibiting immunoglobulin(TEII) level and visual analogue scales (VAS) about fatigue and palpitation were measured before and after administration. Thirteen patients have completed the entire follow-up of this study over two months. Results: Serum levels of T3 and FT4 were significantly improved by AJBHT(T3: 298.85$\pm$79.60 ng/dl 181.15$\pm$33.92 ng/dl p<0.0001, FT4: 2.78$\pm$1.06 ng/dl$\rightarrow$1.78$\pm$0.83 ng/dl p<0.05). However, there were no significant changes in TSH and TBII values. And the VAS scores of fatigue and palpitation also were significantly improved(5.80$\pm$3.01$\rightarrow$3.60$\pm$2.63, p<0.05; 6.19$\pm$2.09$\rightarrow$3.60$\pm$2.46, p<0.01). Patients' age was related to the post-treatment FT4 values(p<0.05). Conclusions: From these results, we suggest that AJBHT is effective on the TFT and the symptoms of Graves' disease, and is a safe alternative drug for Graves' disease patients.

• Journal of Pharmaceutical Investigation
• /
• 제9권2호
• /
• pp.11-21
• /
• 1979

It has been reported from our department that a few agents, such as $K_2S_2O_5,\;NaHSO_3,$ nicotinamide have a marked stabilizing effect in vitro on metoclopramide which is relatively unstable compound. In order to study the effect of these stabilizers on the action of metoclopramide in vitro, the fate of this compound combined with $K_2S_2O_5,\;NaHSO_3$ and nicotinamide, respectively, was studied and furthermore, the change of the biological activity of metoclopramide due to these stabilizers was studied by using the isolated stomach strip of rat. The blood concentration of metoclopramide was measured by using Bakke's method at the various time after intravenous injection of the mixed metoclopramide solution with the stabilizers. In order to study the excretion of the drug, rabbits were anesthesized and catheterized into bladder for withdrawal of urine. After intravenous injection of the mixed metoclopramide solution, urine was collected for 5 hours and the conjugated forms of metoclopramide as well as the free form were determined by using Arita's method. In the biological study of the metoclopramide combined with stabilizers, the contractability of the isolated rat stomach strip was observed by using polygraph recorder. The results were following: 1. When metoclopramide was administered with nicotinamide as stabilizer, the blood concentration of the unchanged from and the rate of the clearance of this compound were very similar to that of metoclopramide alone. On the other hand, other stabilizers, $K_2S_2O_5\;and\;NaHSO_3$, brought about 40% decrease in blood concentration of the unchanged form at 15 min after intravenous injection however, the rate of clearance of metoclopramide with $K_2S_2O_5\;or\;NaHSO_3$ was very slow. 2. In the case of urinary excretion, the excretory pattern of the metabolites of metoclopramide with $NaHSO_3$ or nicotinamide was very similar to that of metoclopramide alone. But metodopramide plus $K_2S_2O_5$ group showed the maked depression of excretion for first 1 hour. 3. In composition of metabolites, when metoclopramide was administered with $K_2S_2O_5$ or $NaHSO_3$, the sulfonate conjugation was predominant. But the glucuronic acid conjugation was predominant in metoclopramide plus nicotinamide gronp. 4. In the experiments on the biological activity of the metoclopramide, this compound exhibited the marked contracting effect in isolatd rat stomach strip. Specially, the meetoclopramide combined with $K_2S_2O_5$ showed the strong contraction of the isolated strip, suggesting the potenciating effect of $K_2S_2O_5$ on the action of metoclopramide in the isolated strip.

• 대한약침학회지
• /
• 제7권1호
• /
• pp.53-61
• /
• 2004

Substantial evidence suggests that behavioral and reinforcing effects of cocaine can be mediated by the mesolimbic dopaminergic system. It has been shown that repeated injections of cocaine produce increase in locomotor activity, expression of the immediate-early gene, c-fos in the nucleus accumbens (NAc), which was one of the main dopaminergic terminal areas. Herbal-acupuncture as a therapeutic intervention has been widely used for the treatment of many functional disorders such as drug abuse. Coptidis Rhizoma (CR) and its main component, berberine (BER) were selected as herbal medicine of herbal-acupuncture. Both medicines have been known to have the therapeutic effect on the central nervous system. In order to investigate the effects of CR and BER herbalacupuncture at shenmen (HT7) point (CR/H and BER/H) on the cocaine-induced behavioral sensitization, the influence of CR/H and BER/H on repeated cocaine-induced locomotor activity, the change of c-Fos expression in the brain by immunohistochemistry were examined. Male SD rats were given CR/H (0.4mg/kg) and BER/H (0.1mg/kg) 30 min before daily injections of cocaine hydrochloride (15mg/kg. i.p.) 10 days. After 3 days withdrawal, rats received a challenge injection of cocaine (15mg/kg, i.p.). Systemic challenge with cocaine produced much larger increased locomotor activity, accumbal Fos-like immunoreactivity in the NAc. Pretreatment with CR/H and BER/H significantly inhibited cocaine-induced locomotor activity, the change of c-Fos expression in the rats. Our data demonstrated that the inhibitory effects of cocaine-induced behavioral sensitization by CR/H and BER/H were closely associated with the reduction of presynaptic dopamine release in the NAc. These results suggest that CR/H and BER/H can be effectively applied to cocaine addiction.

• Journal of Animal Science and Technology
• /
• 제63권1호
• /
• pp.36-45
• /
• 2021

Presently, there is an increased demand for livestock products all over the world which has led to more devotion on improving livestock population. Although goats have been bred for a long time in Korea, but there is not much research conducted on traditional Korean black goat (Capra hircus coreanae) compared to other livestock populations. Mutton consumption has been dramatically changing from medicinal use to edible meat and this trend directs the black goat populations declining and also mutton import quantities are increasing consistently. The present study introduced a new estrus synchronizing technique with subsequent artificial insemination (AI) for Korean black goats to enable crossbreeding with non-native breeds for the small or subsistent farmers. Our data highlighted that, the percentage of motile sperm from the electro-ejaculated samples declined significantly after freezing and melting. In addition, the sperm motility significantly declined with regard to sperm incubation period (0, 5, 60, and 120 min at 37℃) and was negatively correlated (64.2 ± 7.9%, 63.3 ± 5.8%, 49.9 ± 6.3%, and 35.9 ± 7.6%, respectively) in frozen-thawed sperm samples. Moreover, the E2 levels were unchanged even 24 h after controlled internal drug releas (CIDR) withdrawal. But, 48 h and 72 h after CIDR removal, E2 levels increased significantly. These data helps us to consider the two time points for AI; CIDR removal after 24 h, at which E2 decreases, and after 48 h, as the time at which progesterone increases. Additionally, the AI after 48 h of CIDR removal group exhibited significantly higher pregnancy and parturition rates (42.9%) compared to AI after 24 h after CIDR removal 28.6% group. In conclusion, these studies will propose an optimal estrus synchronisation process with subsequent timing of AI and also will promote the Korean black goat breeding industry.

• Clinical and Experimental Pediatrics
• /
• 제53권4호
• /
• pp.560-564
• /
• 2010

목 적 : 항경련제는 대뇌의 여러 신경전달물질의 합성과 분비, 대사과정에 영향을 미쳐 간질파의 발생을 변화시키고 임상적인 경련 조절 효과를 나타낸다. 저자들은 소아 간질 환자에서 항경련제 치료 후 뇌파의 간질파 변화와 이에 영향을 미치는 인자를 알아보고자 이 연구를 시행하였다. 방 법: 2001년 1월부터 2007년 12월까지 부산대학교병원 소아청소년과에서 뇌파 검사를 시행한 후 소아 간질로 처음 진단받고 최소 6개월 이상 항경련제 치료를 지속한 환자 중 6-12개월 간격으로 정기적인 뇌파검사를 시행한 만 1세에서 15세까지의 257명(남아 151명, 여아 106명)의 환아를 대상으로 하였다. 항경련제의 투여 전과 최근의 뇌파를 기준으로 간질파 유무에 따라 네 군으로 나누어 성별, 진단 시 연령, 경련 형태, 간질 원인, 치료 기간, 사용한 항경련의 개수, 경련 조절 여부 등을 비교분석 하였다. 결 과: 대상 환아의 치료 시작 시 평균 연령은 $6.79{\pm}3.40$세였고, 평균 추적관찰기간은 $2.48{\pm}1.85$년이었다. 항경련제 치료 전후 간질파에 변화가 없는 환아는 176명(68.5%), 간질파가 변한 환아는 81명(31.5%)이었다. 항경련제 치료 전후 모두 간질파를 보인 군(1군)은 110명(42.8%), 치료 전 간질파가 있었으나 치료 후 간질파가 사라진 군(2군)은 61명(23.7%), 치료 전에 간질파가 없었으나 치료 후 간질파를 보인 군(3군)은 20명(7.8%), 치료 전후 간질파가 모두 없던 군(4군)은 66명(25.7%)이었다. 약물치료 기간은 1군에서 $2.42{\pm}1.81$년, 2군에서 $3.06{\pm}1.80$년, 3군에서 $2.75{\pm}1.94$년, 4군에서 $1.95{\pm}1.81$년으로, 치료 전에 간질파가 있었으나 치료 후 간질파가 소실된 2군에서 약물 치료 기간이 의미 있게 가장 길었다($P$=0.007). 경련 형태에서 전신 발작을 보인 경우는 1군에서 18.2% (20/110례), 2군에서 31.1% (19/61례), 3군에서 20.0% (4/20례), 4군에서 43.9% (29/66례)로 최종 뇌파 검사에서 간질파가 없었던 2, 4군에서 전신 발작이 유의하게 많았다($P$=0.002). 그 외 각 군에서 성별, 간질 원인, 사용한 항경련제의 개수, 발작 조절 여부, 진단 시 뇌파에 배경파 이상 유무에 의미 있는 차이는 없었다. 결 론: 간질파의 출현은 항경련제 치료 중 1/3의 환자에서 변화가 있었으며 최종 뇌파에서 간질파가 없는 군에서 전신 발작의 환자가 많았다.