Influence of endometriosis on pain behaviors and muscle hyperalgesia induced by a ureteral calculosis in female rats

• Published in: Pain (Amsterdam) Vol. 95; no. 3; pp. 247 - 257
• Main Authors: Giamberardino, Maria Adele, Berkley, Karen J, Affaitati, Giannapia, Lerza, Rosanna, Centurione, Lucia, Lapenna, Domenico, Vecchiet, Leonardo
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 01-02-2002; Lippincott Williams & Wilkins, Inc; Elsevier
• Subjects: Abdominal Muscles; Animals; Anti-Inflammatory Agents, Non-Steroidal - pharmacology; Behavior, Animal; Biological and medical sciences; Colic; Colic - drug therapy; Colic - etiology; Colic - physiopathology; Cysts - pathology; Endometriosis - pathology; Endometriosis - physiopathology; Female; Female genital diseases; Gynecology. Andrology. Obstetrics; Hyperalgesia - drug therapy; Hyperalgesia - etiology; Hyperalgesia - physiopathology; Hysterectomy; Ketoprofen; Ketoprofen - pharmacology; Medical sciences; Non tumoral diseases; Pelvic pain; Pelvic Pain - drug therapy; Pelvic Pain - etiology; Pelvic Pain - physiopathology; Pressure; Rats; Rats, Sprague-Dawley; Ureteral Calculi - complications; Urinary tract; Uterus; Hysterectomy; Urinary tract; Uterus; Pelvic pain; Colic; Ketoprofen; Urethral disease; Rat; Rodentia; Endometriosis; Urinary tract disease; Striated muscle; Female genital diseases; Urinary stone; Hyperalgesia; Vertebrata; Referred pain; Mammalia; Pain; Animal; Uterine diseases; Female
• ISSN: 0304-3959; 1872-6623
• DOI: 10.1016/S0304-3959(01)00405-5

Endometriosis and urinary calculosis can co-occur. Clinical studies have shown that both painful and non-painful endometriosis in women are associated with enhanced pain and referred muscle hyperalgesia from urinary calculosis, but the mechanisms underlying this phenomenon are still poorly understood. The aim of this study was to develop an animal model adequate to explore this viscero-visceral interaction in standardized conditions.
Using a model of endometriosis previously developed to study reduced fertility and vaginal hyperalgesia, endometriosis (
endo) or sham-endometriosis (
sham-endo) was induced in rats by autotransplantation of small pieces of uterus (or, for
sham-endo, fat) on cascade mesenteric arteries, ovary, and abdominal wall. After the endometrial, but not the fat autografts had produced fluid-filled cysts (3 weeks), urinary calculosis was induced by implanting an artificial stone into one ureter. Pain behaviors were monitored by continuous 24-h videotape recordings before and after stone implantation. Referred muscle hyperalgesia was assessed by measuring vocalization thresholds to electrical stimulation of the oblique musculature (L1 dermatome). The data were compared with previously reported data from rats that had received only the stone. Neither
endo nor
sham-endo alone induced pain behaviors. Following stone implantation, in
endo rats compared to
sham-endo and
stone-only rats, pain behaviors specifically associated with urinary calculosis were significantly increased and new pain behaviors specifically associated with uterine pathology became evident. Muscle hyperalgesia was also significantly increased. To explore the relationship between the amount of endometriosis and that of ureteral pain behavior, two separate groups of
endo rats were treated with either a standard non-steroidal anti-inflammatory drugs (ketoprofen) or placebo from the 12th to the 18th day after endometriosis induction. The stone was implanted on the 21st day. Ketoprofen treatment compared to placebo significantly reduced the size of the cysts and both ureteral and uterine pain behaviors post-stone implantation. The size of the cysts showed a significant linear correlation with the post-stone ureteral pain behaviors. In conclusion,
endo increased pain crises and muscle hyperalgesia typically induced by a ureteral calculosis, and the ureteral calculosis revealed additional pain behaviors typically induced by uterine pathophysiology; and this enhancement was a function of the degree of endometriosis. This result closely reproduces the condition observed in humans and could be due to a phenomenon of ‘viscero-visceral’ hyperalgesia, in which increased input from the cyst implantation sites to common spinal cord segments (T10-L1) facilitates the central effect of input from the urinary tract.