Pregabalin as a Pain Therapeutic: Beyond Calcium Channels DOI Creative Commons
Sascha R.A. Alles, Stuart M. Cain, Terrance P. Snutch

и другие.

Frontiers in Cellular Neuroscience, Год журнала: 2020, Номер 14

Опубликована: Апрель 15, 2020

Initially developed with the aim of generating new treatments for epilepsy, gabapentin and pregabalin ("gabapentinoids") were engineered to mimic action GABA modulate metabolism. Rather than their intended pharmacological on neurotransmission, instead they exhibit a high affinity α2δ-1and -2 subunits voltage-activated calcium channels, wherein binding gabapentinoids inhibits cellular influx attenuates neurotransmission. Despite lack activity levels, are effective at suppressing seizures subsequently approved as class antiepileptic therapy partial-onset epilepsy. Through same hypothesized molecular mechanism by controlling neuronal hyperexcitability, demonstrate clear efficacy in pain management, which has arguably been most extensively prescribed application date. In this review, we focus second-generation gabapentinoid widely employed treatment variety conditions. We also discuss wider functional roles  contributions that might play affecting physiological pathophysiological processes.

Язык: Английский

The Neuroimmunology of Chronic Pain: From Rodents to Humans DOI Creative Commons
Peter M. Grace, Vivianne L. Tawfik, Camilla I. Svensson

и другие.

Journal of Neuroscience, Год журнала: 2020, Номер 41(5), С. 855 - 865

Опубликована: Ноя. 25, 2020

Chronic pain, encompassing conditions, such as low back arthritis, persistent post-surgical fibromyalgia, and neuropathic pain disorders, is highly prevalent but remains poorly treated. The vast majority of therapeutics are directed solely at neurons, despite the fact that signaling between immune cells, glia, neurons now recognized indispensable for initiation maintenance chronic pain. This review highlights recent advances in understanding fundamental neuroimmune mechanisms novel therapeutic targets rodent models We further discuss new technological developments to study, diagnose, quantify contributions patient populations.

Язык: Английский

Процитировано

96

Alloknesis and hyperknesis—mechanisms, assessment methodology, and clinical implications of itch sensitization DOI
Hjalte Holm Andersen, Tasuku Akiyama, Leigh Nattkemper

и другие.

Pain, Год журнала: 2018, Номер 159(7), С. 1185 - 1197

Опубликована: Апрель 11, 2018

Abstract Itch and pain share numerous mechanistic similarities. Patients with chronic itch conditions (for instance atopic dermatitis or neuropathic itch) often experience symptoms such as mechanical alloknesis hyperknesis. These dysesthesias are analogous to the pain-associated phenomena allodynia hyperalgesia, which observed, for example, in conditions. Mechanical represent abnormal sensory states (caused by neuroplastic changes), wherein considerable is evoked, light cutaneous stimuli from clothing (alloknesis), where increased perceived response normally itch-evoking (hyperknesis). sensitization have been explored experimental human studies, observed patients, animal models of itch. Limited attention has paid these clinical it unknown how they respond antipruritics. Psychophysical quantitative testing can quantify presence, severity, spatial extent providing a proxy measurement sensitization. This review outlines current assessment techniques, knowledge on mechanisms hyperknesis, presents diverse results derived studies exploring presence patients. A key role neuronal patients accepted used assessments. However, precise potential implications remain be evaluated.

Язык: Английский

Процитировано

91

Effects of Herbal Medicines on Pain Management DOI
Yun Luo, Chong‐Zhi Wang,

Richard Sawadogo

и другие.

The American Journal of Chinese Medicine, Год журнала: 2020, Номер 48(01), С. 1 - 16

Опубликована: Янв. 1, 2020

Pain is an unpleasant sensory and emotional experience in many diseases often caused by intense or damaging stimuli. negatively affects the quality of life increases high health expenditures. Drugs with analgesic properties are commonly used to relieve pain, but these Western medications could be overwhelmed side effects including tolerance addiction. Herbal medicines may provide alternative measures for pain management. In this review paper, after introduction Chinese medicine theory treatment modality, emphasis placed on application herbs herbal formulations Three most herbs, i.e., Corydalis yanhusuo, Ligusticum chuanxiong, Aconitum carmichaeli, reviewed. Subsequently, using ancient medical remedy, formulation treating common conditions associated such as headache/migraine, chest abdominal low back neuropathic osteoarthritis, cancer presented. considered a complementary integrative approach modern armamentarium combating pain.

Язык: Английский

Процитировано

79

Estrogen receptors in pain modulation: cellular signaling DOI Creative Commons
Qing Chen, Wenxin Zhang,

Neeti Sadana

и другие.

Biology of Sex Differences, Год журнала: 2021, Номер 12(1)

Опубликована: Фев. 10, 2021

Sensory perception and emotional disorders are disproportionally represented in men women thus thought to be modulated by different sex hormones various conditions. Among the most important perceived affect sensory processing transduction is estrogen. Numerous previous researchers have endeavored demonstrate that estrogen capable of modulating activity neurons peripheral central sites female, male, or castrated animals. However, underlying mechanisms its modulation neuronal somewhat unclear. In present review, we discuss possible cellular molecular involved nociception

Язык: Английский

Процитировано

77

Pregabalin as a Pain Therapeutic: Beyond Calcium Channels DOI Creative Commons
Sascha R.A. Alles, Stuart M. Cain, Terrance P. Snutch

и другие.

Frontiers in Cellular Neuroscience, Год журнала: 2020, Номер 14

Опубликована: Апрель 15, 2020

Initially developed with the aim of generating new treatments for epilepsy, gabapentin and pregabalin ("gabapentinoids") were engineered to mimic action GABA modulate metabolism. Rather than their intended pharmacological on neurotransmission, instead they exhibit a high affinity α2δ-1and -2 subunits voltage-activated calcium channels, wherein binding gabapentinoids inhibits cellular influx attenuates neurotransmission. Despite lack activity levels, are effective at suppressing seizures subsequently approved as class antiepileptic therapy partial-onset epilepsy. Through same hypothesized molecular mechanism by controlling neuronal hyperexcitability, demonstrate clear efficacy in pain management, which has arguably been most extensively prescribed application date. In this review, we focus second-generation gabapentinoid widely employed treatment variety conditions. We also discuss wider functional roles  contributions that might play affecting physiological pathophysiological processes.

Язык: Английский

Процитировано

76