Chronic pain defined as pain that persists beyond the period of healing, in the absence of ongoing pathology, usually means pain over 3 to 6 months after the cure of the original disease. In this situation, the pain itself loses its protective function only to fall into a disease entity. There have been many efforts to treat chronic pain, with analgesics being the most commonly used modality, which include non-steroidal anti-inflammatory drug, opioids, antidepressant, and anxiolytic agents. Pain clinicians especially use nerve blocks for the control of intractable pain. Although the effect of nerve block or trigger point injection with local anesthetics is temporary, its effect of breaking the vicious cycle of pain patheway gives a long-term effect of analgesia. There are many diseases managed at pain clinics, including headache, trigeminal neuralgia, neck and shoulder pain, low back pain, complex regional pain syndrome, herpes zoster and postherpetic neuralgia, fantom pain, peripheral neuralgia, and vascular disease. The main nerve indicated for pain control may be any kind of somatic and sympathetic nerves and ganglions responsible for the pain.
Analgesia ; Analgesics ; Analgesics, Opioid ; Anesthetics, Local ; Anti-Anxiety Agents ; Chronic Pain* ; Ganglion Cysts ; Headache ; Herpes Zoster ; Low Back Pain ; Neck ; Nerve Block ; Neuralgia ; Neuralgia, Postherpetic ; Pain Clinics ; Pain, Intractable ; Pathology ; Shoulder Pain ; Trigeminal Neuralgia ; Trigger Points ; Vascular Diseases

The effect of isoflurane and propofol anesthesia upon the infarct size after middle cerebral artery occlusion was studied using 18 male Sprague-Dawley rat. The infarct area was calculated using Quantimet autoradiography and compared between conscious control and anesthe-tized rats. The results were as follows; 1) Slightly increased volume of infarction was noted in anesthetized rat with no significancy compare to conscious control rats, but the caudate nucleus revealed statistically significant increased vloume of infarction in isoflurane anesthesia rats. 2) The protective effect for cerebral ischaemia of isoflurane or propofol seems insignificant, but we can use them in the neuroanesthetic field without difficulty because they do not increase the infarcted volume. 3) Durging iaoflurane anesthesia the elevated brain glucose and glucose-6-phosphate may increase neurological damage after ischaemia. Furthermore the change of CBF/Metabolism relationship may affect to the infarction.
Anesthesia ; Animals ; Autoradiography ; Brain ; Brain Ischemia* ; Caudate Nucleus ; Glucose ; Glucose-6-Phosphate ; Humans ; Infarction ; Infarction, Middle Cerebral Artery ; Isoflurane* ; Male ; Propofol* ; Rats ; Rats, Sprague-Dawley

The effect of isoflurane and propofol anesthesia upon the infarct size after middle cerebral artery occlusion was studied using 18 male Sprague-Dawley rat. The infarct area was calculated using Quantimet autoradiography and compared between conscious control and anesthe-tized rats. The results were as follows; 1) Slightly increased volume of infarction was noted in anesthetized rat with no significancy compare to conscious control rats, but the caudate nucleus revealed statistically significant increased vloume of infarction in isoflurane anesthesia rats. 2) The protective effect for cerebral ischaemia of isoflurane or propofol seems insignificant, but we can use them in the neuroanesthetic field without difficulty because they do not increase the infarcted volume. 3) Durging iaoflurane anesthesia the elevated brain glucose and glucose-6-phosphate may increase neurological damage after ischaemia. Furthermore the change of CBF/Metabolism relationship may affect to the infarction.
Anesthesia ; Animals ; Autoradiography ; Brain ; Brain Ischemia* ; Caudate Nucleus ; Glucose ; Glucose-6-Phosphate ; Humans ; Infarction ; Infarction, Middle Cerebral Artery ; Isoflurane* ; Male ; Propofol* ; Rats ; Rats, Sprague-Dawley

No abstract available.
Cryptococcosis* ; Hybridomas* ; Immunity, Cellular* ; T-Lymphocytes*

No abstract available.
Cryptococcosis* ; Hybridomas* ; Immunity, Cellular* ; T-Lymphocytes*

The influence of Propofol on regional cerebral function and CBF were studied using 24 male Spragus-Dawley rat by quantitative autoradiographic technique for glucose ( (14C)deoxyglucose) and (14C) Iodoantipyrine. Rats had both femoral artery and vein cannulated and were placed on lead weight. Propofol was infused intravenously at a rate of 0.35 mg/kg/min. for induction and 0.3 mg/kg/min for maintenance untill loss of corneal reflex with stable vital signs. Local cerebral glucose utilization and CBF were checked from conscious control rats and propofol anesthetized rats. The results were as follows; 1) There was no physiologically significant effect of propofol on body temperature, MAP, PaCO, and pH. 2) Regional cerebral glucose utilization was markedly decreased in many, but not all, cerebral structures. 3) The order of decreased glucose utilization was Diencephalone>Telencephalone>Mesence-phalone>Mylencephalone. which means the forebrain was more affected than hindbrain. 4) The most affected area of glucose utilization were cerebral association area, visual system and sensory motor cortex, but the auditory system was not so much affected. 5) During combined use of N,O and propofol, there was no significant stimulation effect of N,O to propofol in glucose utilization. 6) Regional CBF were markedly decreased in many brain regions which means low local cerebral glucose utilization with low CBF. 7) Propofol has specific effect of lowering cerebral metabolic rate, CBF, and intracranial pressure but no signigicant effect on cardiovascular system, pulmonary system, or temperature.
Anesthesia* ; Animals ; Body Temperature ; Brain ; Cardiovascular System ; Femoral Artery ; Glucose* ; Humans ; Hydrogen-Ion Concentration ; Intracranial Pressure ; Male ; Motor Cortex ; Propofol* ; Prosencephalon ; Rats* ; Reflex ; Rhombencephalon ; Veins ; Vital Signs

BACKGROUND: Hypertrophic scars and keloids have been regarded as representative of the proliferative change of the connective tissue of the dermis. Clinically, postburn and surgical scars show a smooth, shiny, erythematous appearance at an early stage. It is readily conceivable that, in such scars, changes may take place not only in the dermis but also in the epidermis and, possibly in the stratum corneum (SC). However, in contrast to the tremendous number of studies of scars on the dermis, those studies focusing on the epidermis and the SC have been scarce. OBJECTIVE: We have focused on the function of the SC covering the post-burn scar tissue and keloids. METHODS: Using noninvasive bioengineering measurements of functional properties of the SC, such as transepidermal water loss(TEWL), we evaluated the SC barrier function in various types of healing wounds, such as early erythematous lesion, hypertrophic scar, keloid, healed atrophic scar, scar occurring at the recipient site of the skin grafts and the adjacent normal appearing skin for control. RESULTS: 1. The TEWL values were 14.9+/-7.3 in early erythematous lesions, 13.2+/-7.5 in hypertrophic scars, 10.2+/-5.8 in keloids, 5.6+/-1.3 in healed atrophic scars, 6.9+/-4.3 in scars occurring at the recipient site of the skin grafts. Significantly increased TEWL values were found in all individual lesions(p>0.01) except for the scars occurring at the recipient site of the skin grafts(p<0.05) compared with the corresponding normal control skin. 2. When we randomly compared early erythematous lesions, hypertrophic scars, kelids, atrophic
Bioengineering ; Cicatrix ; Cicatrix, Hypertrophic* ; Connective Tissue ; Dermis ; Epidermis ; Keloid* ; Skin* ; Transplants ; Wounds and Injuries

The effect of inhalation anesthetics on memory was studied using 26 male Sprague-Dawley rats. In the control group the trained rats were tested the first performance time of T-maze and left them to anesthetic chamber for 120min. and checked second performance time 24hours later (Group A). For the experimental group the first performance time was tested and animals were exposed to the anesthetics (1% Halothane with N20:02=2:1) for 120min. and checked second performance time 24hours after cessation of exposure to evaluate retrograde amnesia (Group B). For the test of anterograde amnesia (Group C) rats were anesthetized before test the first performance time and checked second performance time 24hours later. The mean perfor- mance ratio (II/I) (i.e., I is the score in the first performance time and II is the score in the second performance time) was compared between anesthetized and non-anesthetized control group. In the group A the ratio was 102.8+/-19 but in group B it was 96.4+/-13 during anesthesia, 79.+/-19 after anesthesia and 92.3+/-11 in overaU anesthetized group, and was 100.2+/-17 in group C. All data of group B were significantly different with group A (p<0.01). But no statistical difference between group C and A was observed (p=0.174). These results suggest that post- training exposure to volatile anesthetics facilitates memory and no anterograde amnesia observed by pretraining exposure. These may be volatile anesthetics facilitate memory by enhancement of memory consolidation and/or retention or interference reduction.
Amnesia, Anterograde ; Amnesia, Retrograde ; Anesthesia ; Anesthetics ; Anesthetics, Inhalation* ; Animals ; Halothane ; Humans ; Inhalation* ; Male ; Memory* ; Rats* ; Rats, Sprague-Dawley

BACKGROUND: Onset of rocuronium is rapid but relatively large doses are needed to achieve a suitable intubating condition. So we compared the single bolus injection with divided injection of rocuronium about tlie onset time, intubation time and intubating condition. METHOD: Thirty patients were divided into three groups of 10 each randomly. Patients in group I were given a single dose of 0.6mg/kg rocuronium. Those in group 2I or 3 received 0.06 mg/kg or 0.09 mg/kg as priming dose followed by 0.54 mg/kg and 0.81 mg/kg as intubating dose 3 min. later. The train of four responses of adductor pollicis muscle was recorded using Paragraph(Utah Medical Product Inc. Midvale Utah, U.S.A.) every 10 seconds. The trachea was intubated by one clinician who was blinded to the muscle relaxant administered when he thought the patients were suitable for intubation, and he recorded the intubating conditions. The endotracheal intubation time and twitch height at the moment was recorded by other clinician. The onset time was recorded when the post tetanic count is marked as '0'. RESULT: The onset time of group 1, 2, and 3 were 90.0+/-22.lsec, 109.0+/-35.0 sec and 85.0+/-35.0 sec. respectively. Endotracheal intubation times were 77.0+/-10.6sec, 60.0+/-10.0sec and 44.0+/-5.2sec respectively. CONCLUSION: There was no differences about onset time between single and devided injection with same total dose or incremental dose of 0.9mg/kg. But the intubation time was faster in priming group with dose dependent manner, and the intubating conditions were excellent to good in all patients.
Humans ; Intubation* ; Intubation, Intratracheal ; Trachea ; Utah

The effect of anticholinergics on memory was studied using 32 male Sprague-Dawley rats. In the control group the trained rats were tested the first performance time of T-maze and the second performance time checked 4-6 hours after injection of 1.0-1.5 mL of normal saline via penile vein. For the experimental groups, after checking the first performance time, 0.1 mg/kg of atropine sulfate in group B, and 1.0 mg/kg in group C was injected via penile vein.And 30 mg/kg injected into intraperitoneal cavity in group D. But for the group E, the mixture of 1.0 mg/kg of atropine and 0.01 mg/kg of neostigmine was injected into the penile vein. 4-6 hours after injection the second performance time was checked and continued these sets of experiment once a day for 6 days. To compare the number of errors (the qualitative effect) the accuracy rate (Number of right trials/Number of total trials x 100) was checked. To eompare the running time (the quantitative effect) the mean performance ratio (II/I x 100) (i.e., I is the score in the first performance time and II is the score in the second performance time) was compared between control and experimental groups. The results were as follows ; 1) The percentage of correct performance was 84.2% in control group, but 86.1% in group B, 91.0% in C, 96.0% in D and 89.6% in E was noted. 2) The performance ratio of control group A was 100.2 but 82.4 in B, 94.7 in C, 83.2 in D and 89.4 in E was recorded. 3) These results suggest that posttraining exposure to atropine sulfate facilitates the accuracy of performance and shortens the running time and no different effect was observed by additional injection of neostigmine in rats.
Animals ; Atropine* ; Cholinergic Antagonists ; Humans ; Male ; Memory* ; Neostigmine* ; Rats* ; Rats, Sprague-Dawley ; Running ; Veins