TY - JOUR
T1 - Platelet protein kinase C and brain-derived neurotrophic factor levels in borderline personality disorder patients
AU - Koenigsberg, Harold W.
AU - Yuan, Peixiong
AU - Diaz, George A.
AU - Guerreri, Stephanie
AU - Dorantes, Christine
AU - Mayson, Sarah Jo
AU - Zamfirescu, Constantin
AU - New, Antonia S.
AU - Goodman, Marianne
AU - Manji, Husseini K.
AU - Siever, Larry J.
N1 - Funding Information:
This work was supported by the James J Peters Veterans Affairs Medical Center and a grant from the National Center for Research Resources, National Institutes for Health for the Mount Sinai General Clinical Research Center ( 5MO1 RR00071 ).
PY - 2012/9/30
Y1 - 2012/9/30
N2 - Borderline personality disorder (BPD) is a prevalent and difficult to treat psychiatric condition characterized by abrupt mood swings, intense anger and depression, unstable interpersonal relationships, impulsive self-destructive behavior and a suicide rate of approximately 10%. Possible underlying molecular dysregulations in BPD have not been well explored. Protein kinase C (PKC) and brain-derived neurotrophic factor (BDNF) have both been implicated in affective disorders, but their role in BPD has not been examined. Platelets were isolated from blood obtained from 24 medication-free BPD patients and 18 healthy control subjects. PKC-α, phosphorylated-PKC-α (p-PKCα), PKC-ΒII, and BDNF were measured in platelet homogenates by immunoblotting. In the males, platelet BDNF and PKC-α levels were lower in patients than controls. p-PKC-α and PKC-ΒII were lower at trend levels. In the entire sample, platelet p-PKCα and PKC-α activity were lower, at a trend level, in patients compared to controls. This is the first report to our knowledge of PKC and BDNF activity in BPD and calls for replication. These findings are consistent with altered PKC and BDNF activity in a range of neuropsychiatric conditions including bipolar disorder, depression and suicide.
AB - Borderline personality disorder (BPD) is a prevalent and difficult to treat psychiatric condition characterized by abrupt mood swings, intense anger and depression, unstable interpersonal relationships, impulsive self-destructive behavior and a suicide rate of approximately 10%. Possible underlying molecular dysregulations in BPD have not been well explored. Protein kinase C (PKC) and brain-derived neurotrophic factor (BDNF) have both been implicated in affective disorders, but their role in BPD has not been examined. Platelets were isolated from blood obtained from 24 medication-free BPD patients and 18 healthy control subjects. PKC-α, phosphorylated-PKC-α (p-PKCα), PKC-ΒII, and BDNF were measured in platelet homogenates by immunoblotting. In the males, platelet BDNF and PKC-α levels were lower in patients than controls. p-PKC-α and PKC-ΒII were lower at trend levels. In the entire sample, platelet p-PKCα and PKC-α activity were lower, at a trend level, in patients compared to controls. This is the first report to our knowledge of PKC and BDNF activity in BPD and calls for replication. These findings are consistent with altered PKC and BDNF activity in a range of neuropsychiatric conditions including bipolar disorder, depression and suicide.
KW - BDNF
KW - Borderline personality disorder
KW - Neurotrophic factors
KW - PKC
KW - Personality disorders
KW - Second messengers
UR - http://www.scopus.com/inward/record.url?scp=84869198825&partnerID=8YFLogxK
U2 - 10.1016/j.psychres.2012.04.026
DO - 10.1016/j.psychres.2012.04.026
M3 - Article
C2 - 22633012
AN - SCOPUS:84869198825
SN - 0165-1781
VL - 199
SP - 92
EP - 97
JO - Psychiatry Research
JF - Psychiatry Research
IS - 2
ER -