1.Anatomical basis and clinical research of pelvic autonomic nerve preservation with laparoscopic radical resection for rectal cancer.
Yan LIU ; Xiao-ming LU ; Kai-xiong TAO ; Jian-hua MA ; Kai-lin CAI ; Lin-fang WANG ; Yan-feng NIU ; Guo-bin WANG
Journal of Huazhong University of Science and Technology (Medical Sciences) 2016;36(2):211-214
The clinical effect of laparoscopic rectal cancer curative excision with pelvic autonomic nerve preservation (PANP) was investigated. This study evaluated the frequency of urinary and sexual dysfunction of 149 male patients with middle and low rectal cancer who underwent laparoscopic or open total mesorectal excision with pelvic autonomic nerve preservation (PANP) from March 2011 to March 2013. Eighty-four patients were subjected to laparoscopic surgery, and 65 to open surgery respectively. The patients were followed up for 12 months, interviewed, and administered a standardized questionnaire about postoperative functional outcomes and quality of life. In the laparoscopic group, 13 patients (18.37%) presented transitory postoperative urinary dysfunction, and were medically treated. So did 12 patients (21.82%) in open group. Sexual desire was maintained by 52.86%, un-ability to engage in intercourse by 47.15%, and un-ability to achieve orgasm and ejaculation by 34.29% of the patients in the laparoscopic group. Sexual desire was maintained by 56.36%, un-ability to engage in intercourse by 43.63%, and un-ability to achieve orgasm and ejaculation by 33.73% of the patients in the open group. No significant differences in urinary and sexual dysfunction between the laparoscopic and open rectal resection groups were observed (P>0.05). It was concluded that laparoscopic rectal cancer radical excision with PANP did not aggravate or improve sexual and urinary dysfunction.
Adult
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Autonomic Nervous System
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injuries
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Humans
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Laparoscopy
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adverse effects
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Male
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Middle Aged
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Peripheral Nerve Injuries
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etiology
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prevention & control
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Postoperative Complications
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Rectal Neoplasms
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surgery
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Sexual Dysfunction, Physiological
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etiology
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Urologic Diseases
;
etiology
2.Various types of total laparoscopic nerve-sparing radical hysterectomies and their effects on bladder function.
Hiroyuki KANAO ; Kazuko FUJIWARA ; Keiko EBISAWA ; Tomonori HADA ; Yoshiaki OTA ; Masaaki ANDOU
Journal of Gynecologic Oncology 2014;25(3):198-205
OBJECTIVE: This study was conducted to ascertain the correlation between preserved pelvic nerve networks and bladder function after laparoscopic nerve-sparing radical hysterectomy. METHODS: Between 2009 and 2011, 53 patients underwent total laparoscopic radical hysterectomies. They were categorized into groups A, B, and C based on the status of preserved pelvic nerve networks: complete preservation of the pelvic nerve plexus (group A, 27 cases); partial preservation (group B, 13 cases); and complete sacrifice (group C, 13 cases). To evaluate bladder function, urodynamic studies were conducted preoperatively and postoperatively at 1, 3, 6, and 12 months after surgery. RESULTS: No significant difference in sensory function was found between groups A and B. However, the sensory function of group C was significantly lower than that of the other groups. Group A had significantly better motor function than groups B and C. No significant difference in motor function was found between groups B and C. Results showed that the sensory nerve is distributed predominantly at the dorsal half of the pelvic nerve networks, but the motor nerve is predominantly distributed at the ventral half. CONCLUSION: Various types of total laparoscopic nerve-sparing radical hysterectomies can be tailored to patients with cervical carcinomas.
Adult
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Aged
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Female
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Humans
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Hypogastric Plexus/injuries
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Hysterectomy/adverse effects/*methods
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Laparoscopy/adverse effects/*methods
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Middle Aged
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Neoplasm Staging
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Pelvis/innervation
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Peripheral Nerve Injuries/etiology/*prevention & control
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Postoperative Period
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Urinary Bladder/*innervation/physiopathology
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Urodynamics
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Uterine Cervical Neoplasms/pathology/*surgery
3.Early intervention of ERK activation in the spinal cord can block initiation of peripheral nerve injury-induced neuropathic pain in rats.
Mei HAN ; Ru-Yi HUANG ; Yi-Min DU ; Zhi-Qi ZHAO ; Yu-Qiu ZHANG
Acta Physiologica Sinica 2011;63(2):106-114
The present study is to investigate whether the extracellular signal-regulated kinase (ERK) and cAMP response element binding protein (CREB) signaling pathway contributes to the initiation of chronic constriction injury (CCI)-induced neuropathic pain in rats. Mechanical allodynia was assessed by measuring the hindpaw withdrawal threshold in response to a calibrated series of von Frey hairs. Thermal hyperalgesia was assessed by measuring the latency of paw withdrawal in response to a radiant heat source. The expressions of phosphor-ERK (pERK) and phosphor-CREB (pCREB) were examined using Western blot analysis and immunohistochemistry. An early robust increase in the expression of pERK on the spinal cords ipsilateral to injury was observed on day 1 after CCI, when the CCI-induced behavioral hypersensitivity had not developed yet. Moreover, the upregulation of pERK expression in ipsilateral spinal cord was associated with the increase in pCREB expression in bilateral spinal cord. Intrathecal administration of mitogen-activated protein kinase kinase (MEK) inhibitor U0126 before CCI can efficiently block and delay the CCI-induced mechanical allodynia and thermal hyperalgesia. These data suggest that activation of ERK and CREB in the spinal cord contributes to the initiation of peripheral nerve injury-induced pain hypersensitivity, and an early intervention strategy should be proposed.
Animals
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Butadienes
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pharmacology
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Cyclic AMP Response Element-Binding Protein
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metabolism
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Enzyme Inhibitors
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pharmacology
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Extracellular Signal-Regulated MAP Kinases
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metabolism
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Hyperalgesia
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etiology
;
physiopathology
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prevention & control
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Male
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Nitriles
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pharmacology
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Pain
;
etiology
;
physiopathology
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prevention & control
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Peripheral Nerve Injuries
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complications
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metabolism
;
physiopathology
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Rats
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Rats, Sprague-Dawley
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Sciatic Neuropathy
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metabolism
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physiopathology
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Spinal Cord
;
metabolism