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      KCI등재 SCI SCIE SCOPUS

      Effective Dosage and Administration Schedule of Oral Alendronate for Non-nociceptive Symptoms in Rats with Chronic Constriction Injury

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      https://www.riss.kr/link?id=A104744125

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      다국어 초록 (Multilingual Abstract)

      We evaluated the efficacy of oral alendronate with different dosing regimens for nonnociceptive symptoms and osteoporosis in a sciatic nerve chronic constriction injury (CCI) model. Male Sprague-Dawley rats (n=60) were subdivided into sham control (SC) group and CCI groups, which were divided according to dosage and time of oral alendronate administration: no treatment (NT), low dosage early (LE), high dosage early (HE), low dosage late (LL) and high dosage late (HL). We measured the thickness and temperature of the hind paw, bone mineral density (BMD) of the tibia, along with tibia bone strength. On the 14th day post-CCI, the HE group showed significant reduction in thickness and temperature (P<0.001). On the 42nd day post-CCI, the HE group showed significant reduction in temperature compared to the NT group (P<0.001). Also, both HE and HL groups showed statistically significant increased tibia BMD (P<0.001), along with increase of tibia bone strength compared to the NT group. Based on these findings, early alendronate in high dosages is effective in the non-nociceptive symptoms; early and late alendronate in high dosages,are effective in preventing bone dystrophic changes in a CCI model.
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      We evaluated the efficacy of oral alendronate with different dosing regimens for nonnociceptive symptoms and osteoporosis in a sciatic nerve chronic constriction injury (CCI) model. Male Sprague-Dawley rats (n=60) were subdivided into sham control (SC...

      We evaluated the efficacy of oral alendronate with different dosing regimens for nonnociceptive symptoms and osteoporosis in a sciatic nerve chronic constriction injury (CCI) model. Male Sprague-Dawley rats (n=60) were subdivided into sham control (SC) group and CCI groups, which were divided according to dosage and time of oral alendronate administration: no treatment (NT), low dosage early (LE), high dosage early (HE), low dosage late (LL) and high dosage late (HL). We measured the thickness and temperature of the hind paw, bone mineral density (BMD) of the tibia, along with tibia bone strength. On the 14th day post-CCI, the HE group showed significant reduction in thickness and temperature (P<0.001). On the 42nd day post-CCI, the HE group showed significant reduction in temperature compared to the NT group (P<0.001). Also, both HE and HL groups showed statistically significant increased tibia BMD (P<0.001), along with increase of tibia bone strength compared to the NT group. Based on these findings, early alendronate in high dosages is effective in the non-nociceptive symptoms; early and late alendronate in high dosages,are effective in preventing bone dystrophic changes in a CCI model.

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      참고문헌 (Reference)

      1 Burr DB, "Tissue mineralization is increased following 1-yr treatment with high doses of bisphosphonates in dogs" 33 : 960-969, 2003

      2 Mashiba T, "Suppressed bone turnover by bisphosphonates increases microdamage accumulation and reduces some biomechanical properties in dog rib" 15 : 613-620, 2000

      3 Guo TZ, "Substance P signaling contributes to the vascular and nociceptive abnormalities observed in a tibial fracture rat model of complex regional pain syndrome type I" 108 : 95-107, 2004

      4 van der Laan L, "Severe complications of reflex sympathetic dystrophy: infection, ulcers, chronic edema, dystonia, and myoclonus" 79 : 424-429, 1998

      5 Manicourt DH, "Role of alendronate in therapy for posttraumatic complex regional pain syndrome type I of the lower extremity" 50 : 3690-3697, 2004

      6 Rodan GA, "Preclinical pharmacology of alendronate" 3 (3): 7-12, 1993

      7 Poplawski ZJ, "Post-traumatic dystrophy of the extremities" 65 : 642-655, 1983

      8 Mackey S, "Pharmacologic therapies for complex regional pain syndrome" 11 : 38-43, 2007

      9 Birklein F, "Pattern of autonomic dysfunction in time course of complex regional pain syndrome" 8 : 79-85, 1998

      10 Suyama H, "Osteoporosis following chronic constriction injury of sciatic nerve in rats" 20 : 91-97, 2002

      1 Burr DB, "Tissue mineralization is increased following 1-yr treatment with high doses of bisphosphonates in dogs" 33 : 960-969, 2003

      2 Mashiba T, "Suppressed bone turnover by bisphosphonates increases microdamage accumulation and reduces some biomechanical properties in dog rib" 15 : 613-620, 2000

      3 Guo TZ, "Substance P signaling contributes to the vascular and nociceptive abnormalities observed in a tibial fracture rat model of complex regional pain syndrome type I" 108 : 95-107, 2004

      4 van der Laan L, "Severe complications of reflex sympathetic dystrophy: infection, ulcers, chronic edema, dystonia, and myoclonus" 79 : 424-429, 1998

      5 Manicourt DH, "Role of alendronate in therapy for posttraumatic complex regional pain syndrome type I of the lower extremity" 50 : 3690-3697, 2004

      6 Rodan GA, "Preclinical pharmacology of alendronate" 3 (3): 7-12, 1993

      7 Poplawski ZJ, "Post-traumatic dystrophy of the extremities" 65 : 642-655, 1983

      8 Mackey S, "Pharmacologic therapies for complex regional pain syndrome" 11 : 38-43, 2007

      9 Birklein F, "Pattern of autonomic dysfunction in time course of complex regional pain syndrome" 8 : 79-85, 1998

      10 Suyama H, "Osteoporosis following chronic constriction injury of sciatic nerve in rats" 20 : 91-97, 2002

      11 Huygen FJ, "Neuroimmune alterations in the complex regional pain syndrome" 429 : 101-113, 2001

      12 Daemen MA, "Neurogenic inflammation in an animal model of neuropathic pain" 20 : 41-45, 1998

      13 Daemen M, "Neurogenic inflammation and reflex sympathetic dystrophy (in vivo and in vitro assessment in an experimental model)" 64 : 441-447, 1998

      14 Varenna M, "Intravenous clodronate in the treatment of reflex sympathetic dystrophy syndrome. A randomized, double blind, placebo controlled study" 27 : 1477-1483, 2000

      15 Schinkel C, "Inflammatory mediators are altered in the acute phase of posttraumatic complex regional pain syndrome" 22 : 235-239, 2006

      16 Guo TZ, "Glucocorticoid inhibition of vascular abnormalities in a tibia fracture rat model of complex regional pain syndrome type I" 121 : 158-167, 2006

      17 Kingery WS, "Glucocorticoid inhibition of neuropathic limb edema and cutaneous neurogenic extravasation" 913 : 140-148, 2001

      18 Robinson JN, "Efficacy of pamidronate in complex regional pain syndrome type I" 5 : 276-280, 2004

      19 Bianchi M, "Effects of the bisphosphonate ibandronate on hyperalgesia, substance P, and cytokine levels in a rat model of persistent inflammatory pain" 12 : 284-292, 2008

      20 Griffin MG, "Dual-energy x-ray absorptiometry of the rat: accuracy, precision, and measurement of bone loss" 8 : 795-800, 1993

      21 Janig W, "Complex regional pain syndrome: mystery explained?" 2 : 687-697, 2003

      22 Coderre TJ, "Chronic post-ischemia pain (CPIP): a novel animal model of complex regional pain syndrome- type I (CRPS-I; reflex sympathetic dystrophy) produced by prolonged hindpaw ischemia and reperfusion in the rat" 112 : 94-105, 2004

      23 Lee JI, "Changes in bone metabolism in a rat model of traumatic brain injury" 19 : 1207-1211, 2005

      24 Adami S, "Bisphosphonate therapy of reflex sympathetic dystrophy syndrome" 56 : 201-204, 1997

      25 Bonabello A, "Analgesic effect of bisphosphonates in mice" 91 : 269-275, 2001

      26 Breuer B, "An openlabel pilot trial of ibandronate for complex regional pain syndrome" 24 : 685-689, 2008

      27 Goicoechea C, "Alendronate induces antinociception in mice, not related with its effects in bone" 79 : 433-437, 1999

      28 Kingery WS, "A substance P receptor (NK1) antagonist enhances the widespread osteoporotic effects of sciatic nerve section" 33 : 927-936, 2003

      29 Bennett GJ, "A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man" 33 : 87-107, 1988

      30 Kingery WS, "A critical review of controlled clinical trials for peripheral neuropathic pain and complex regional pain syndromes" 73 : 123-139, 1997

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 SCI 등재 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.48 0.37 1.06
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.85 0.75 0.691 0.11
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